<i>Salmonella enterica</i>: Survival, Colonization, and Virulence Differences among Serovars

Andino, A.; Hanning, I.

doi:https://doi.org/10.1155/2015/520179

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Review Article | Open Access

Volume 2015 | Article ID 520179 | https://doi.org/10.1155/2015/520179

Salmonella enterica: Survival, Colonization, and Virulence Differences among Serovars

A. Andino¹and I. Hanning¹

Academic Editor: Prerak Desai

Received30 Jul 2014

Revised04 Dec 2014

Accepted15 Dec 2014

Published13 Jan 2015

Abstract

Data indicate that prevalence of specific serovars of Salmonella enterica in human foodborne illness is not correlated with their prevalence in feed. Given that feed is a suboptimal environment for S. enterica, it appears that survival in poultry feed may be an independent factor unrelated to virulence of specific serovars of Salmonella. Additionally, S. enterica serovars appear to have different host specificity and the ability to cause disease in those hosts is also serovar dependent. These differences among the serovars may be related to gene presence or absence and expression levels of those genes. With a better understanding of serovar specificity, mitigation methods can be implemented to control Salmonella at preharvest and postharvest levels.

1. Introduction

Salmonellae are facultative anaerobic Gram-negative rod-shaped bacteria generally 2–5 microns long by 0.5–1.5 microns wide and motile by peritrichous flagella. Genome sizes of Salmonella vary among serovars (Table 1) with ranges from 4460 to 4857 kb. Salmonellae belong to the family Enterobacteriaceae and are a medically important pathogen for both humans and animals. Salmonellae form a complex group of bacteria consisting of two species and six subspecies and include more than 2,579 serovars [1, 2]. Two species are currently recognized in the genus Salmonella, S. enterica and S. bongori [3]. S. enterica can be subdivided into the subspecies enterica, salamae, arizonae, diarizonae, houtenae, and indica based on biochemical and genomic modifications [4]. The majority of Salmonellae are lactose fermenters, hydrogen sulfite producers, oxidase negative, and catalase positive. Other biochemical properties that allow identification of Salmonella include the ability to grow on citrate as a sole carbon source, decarboxylate lysine, and hydrolyze urea [5, 6].

The main niche of Salmonella serovars is the intestinal tract of humans and farm animals. It can also be present in the intestinal tract of wild birds, reptiles, and occasionally insects. Feedstuff, soil, bedding, litter, and fecal matter are commonly identified as sources of Salmonella contamination in farms [7–10]. As Salmonella colonizes the gastrointestinal tract, the organisms are excreted in feces from which they may be transmitted by insects and other animals to a large number of places and are generally found in polluted water. Salmonellae do not originate in water; therefore their presence denotes fecal contamination [6]. Humans and animals that consume polluted water may shed the bacteria through fecal matter continuing of the cycle of contamination.

Like many other infectious diseases, the course and outcome of the infection depend on variable factors including the dose of inoculation and the immune status of the host [11]. In the US, Salmonella is the leading foodborne pathogen, causing the largest number of deaths and has the highest cost burden [12]. The annual costs associated with salmonellosis for 2010 were estimated at $2.71 billion for 1.4 million cases [13]. The highest numbers of Salmonella outbreaks from the past decade are related to land animals, with poultry as a main reservoir (Table 2). More than 70% of human salmonellosis in the US has been attributed to the consumption of contaminated chicken, turkey, or eggs [14]. From 1998 to 2008, approximately 145 Salmonella outbreaks have been associated with poultry while 117 outbreaks were associated with eggs, causing illnesses in 2580 and 2,938 people, respectively [14].

However, a considerable number of outbreaks have been related to crops (Table 3). From 1998 to 2008 fruits and nuts were the highest cause of Salmonella outbreaks in plant products, followed by vine stalk vegetables and sprouts. Sanderson and Demerec [11] reported that Salmonella appears eight times between the top 20 ranked pathogen-food combinations and is most notably associated with poultry, produce, and eggs. It is not always easy to identify specific serovars in an outbreak; in many cases Salmonella cannot be linked to a specific food component due to complex food preparations using a variety of ingredients.

In the US, data from foodborne outbreaks related to human illness collected from 2007 to 2011 reported that 89% were confirmed serotypes [14]. Serovar Enteritidis was the most frequently isolated followed by Typhimurium, Newport, Heidelberg, and Montevideo (Table 4). The food vehicles associated with this serovars include a wide variety of products including eggs, chicken, pork, leafy greens, peanut butter, turkey, dairy products, and vegetables (Table 4).

Salmonellae can enter and survive in the farm environment for long periods of time. Prevalence of Salmonella in farm environments ranges from 10 to 26% according to a recent study [9]. Presence of Salmonella in feed and feed ingredients is well documented [9, 31–33]. However, very low levels of Salmonella have been obtained from drinking water samples from broiler farms. Conversely, recovery of Salmonella was easily accomplished in samples from standing water where the bacteria can persist in biofilms [31, 32, 34]. Variety and prevalence of Salmonella serovars differ among studies in different regions and types of farms. Yet, there is some consistency in recovery rates of specific serovars: Heidelberg, Kentucky, Enteritidis, Typhimurium, Montevideo, Seftenberg, and Thompson as these are the highest recovered serotypes [32, 34, 35]. In a one year experiment in an integrated operation, Bailey et al. [32] found that hatchery transport pads, flies, drag swabs, and boot swabs exhibited the highest prevalence of Salmonella. The most frequently identified serotypes from those farm samples were Seftenberg, Thompson, and Montevideo. According to reports from the monitoring system by the USDA through the Food and Safety Inspection Service (FSIS), from 2000 to 2009 serotypes Kentucky, Enteritidis, Heidelberg, Typhimurium, and antigenic formula I 4, 5,12:i:- were commonly isolated from broilers (Table 5) and ground chicken (Table 6).

Shell eggs are a major vehicle for S. Enteritidis in humans. By 1994 S. Enteritidis became the most frequent serovar reported in the US causing human salmonellosis. From 1985 to 2003 in 75% of S. Enteritidis outbreak cases, eggs were confirmed as the primary ingredient or food vehicle of contamination [14]. A major outbreak occurred in 1994 where tanker trailers that previously carried S. Enteritidis contaminated liquid eggs cause the cross contamination of ice-cream prepared at the same facility [37]. Serovar Enteritidis is known to be very well adapted to the hen house environment, the bird, and the egg. Most commonly, hens are infected with S. Enteritidis by vertical transmission and through transovarian infection eggs may become contaminated [38]. S. Typhimurium and other serovars usually contaminate eggs externally by penetrating the egg shell [39]. Surveys conducted in US report Salmonella contamination in table eggs by other serovars including Heidelberg and Montevideo [39, 40]. Enhanced biosecurity practices, postharvest intervention methods (sanitizing and decontamination), and egg pasteurization can reduce the risk factors for Salmonella infection in laying hen operations [41].

2. Salmonella Serovar Host Specificity and Disease

2.1. Diseases in Chickens

Birds infected with most Salmonella serovars do not show clinical signs of the disease, making it difficult to diagnose at the farm. However, S. Pullorum and S. Gallinarum do cause disease in poultry but rarely cause illness in humans. These Salmonella serovars are nonmotile and host-specific and cause Pullorum disease (PD) and fowl typhoid (FT), respectively [42].

Pullorum disease was first described as “fatal septicemia” or “white diarrhea” [42]. Clinical signs are predominantly observed in young chickens, showing lack of appetite, depression, respiratory distress, caseous core diarrhea, and early death a few days after hatching. In laying hens symptoms include reduced egg production, fertility, and hatchability [43–45]. Salmonella Pullorum may cause severe systemic lesions including peritonitis and liver and spleen enlargement, and organs may be streaked with hemorrhages; animals can also develop white focal necrosis in the case of young birds and abnormal color and shape in ovaries in older birds. Pullorum disease mortality rate is variable but maybe as high as 100% in critical cases.

Fowl typhoid disease is caused by S. Gallinarum and affects chickens, turkeys, guinea fowl, and birds of all ages and breeds [46]. The first described outbreak was characterized by high mortality and signs of the disease that began with yellow-to-green diarrhea with the birds dying few days after infection [42]. Unlike S. Pullorum, S. Gallinarum is more frequently seen in older birds than young birds. One of the first signs of this disease is an increase in mortality rate, followed by a decline in feed consumption and therefore a drop in egg production and weight gain [44]. Histological examination reveals fatty degeneration of the liver, occasionally accompanied by areas of necrosis, disintegration of muscle fibers, and congestion and perivascular infiltration of mononuclear cells in the kidneys [47].

Salmonella Pullorum and S. Gallinarum have been eradicated in developed regions including the US, Canada, and Western Europe but are still problems in other parts of the world. Control programs that incorporated good hygiene management, biosecurity enforcement, serological tests, and slaughter policies helped with the eradication of these pathogens. In 1935, the US Federal Government executed the National Poultry Improvement Plan (NPIP) in order to reduce the mortality of chickens from Pullorum and Gallinarum disease. In the 1950s, poultry breeders and hatchers in US implemented tests (blood analysis, tube agglutination, and rapid serum test) for S. Pullorum and S. Gallinarum on a regular basis while uniform national management standards were adopted. Furthermore, in the 1950s vaccination was implemented to control Pullorum disease and fowl typhoid. Two decades later both diseases were eradicated and by 1975 there was no evidence of infection in commercial poultry [43, 48, 49].

It has been suggested that clearing poultry flocks of S. Gallinarum and S. Pullorum opened a favorable niche for S. Enteritidis [50–52]. The use of mathematical models with data from Europe and US suggests that S. Gallinarum excluded S. Enteritidis from poultry [53]. Coincidently, S. Enteritidis detection was on the rise after eradication of S. Gallinarum and S. Pullorum, and by the 1990s it was the most frequently reported serovars in the US. Unlike avian Salmonella pathogens, serovar Enteritidis has rodents as reservoirs, making it more difficult to control on the farms. S. Enteritidis and S. Gallinarum are antigenic similar, both belonging to serogroup D1 possessing a similar lipopolysaccharide structure and O9 antigens. When commercial flocks were cleared from S. Gallinarum, serovar Enteritidis was able to colonize chickens without noticeable signs of disease. It is believed that seropositive S. Pullorum had an enhanced immunity dominant O9 antigen that protected against S. Enteritidis infection [50].

2.2. Diseases in Humans

2.2.1. Typhoid and Paratyphoid Fevers

Clinically, salmonellosis may be manifested as gastroenteritis, septicemia, or enteric fever. Enteric fevers are caused by the human-specific pathogens S. enterica serovars Typhi and Paratyphi. Infection severity may vary by the resistance of each individual and the immune system as well as the virulence of the Salmonella isolate.

Salmonella Typhi is a motile, nonlactose fermenting bacillus that causes most endemic and epidemic cases of typhoid fever globally [54, 55]. Enteric fevers cause 200,000 deaths and 22 million illnesses per year, with the highest incidence happening in Southeast and Central Asia where it is endemic [56]. Doses from 10³ to 10⁹ CFU of Salmonella Typhi are known to cause enteric fever [57].

2.2.2. Nontyphoidal Salmonellosis

Like enteric fevers, nontyphoidal salmonellosis (NTS) is spread via the fecal-oral route, but estimated cases of NTS worldwide greatly surpass those for enteric fevers. Unlike Typhi and Paratyphi, nontyphoidal Salmonellae are not human-restricted. Many serovars closely related to foodborne outbreaks include S. Typhimurium, S. Enteritidis, S. Newport, and S. Heidelberg and have reservoirs in farm animals [9, 58]. Among other foodborne pathogens, NTS is the leading cause of death and hospitalizations [59]. In NTS, cases are characterized by gastroenteritis or bacteraemia; symptoms may involve nausea, vomiting, and diarrhea and are typically self-limiting lasting approximately 7 days. Salmonella can also induce chronic conditions including aseptic reactive arthritis and Reiter’s syndrome.

2.3. Differences among Serovars with respect to Disease Severity

Different Salmonella serovars may demonstrate unique reservoirs and pathogeneses. It is still poorly understood why a few Salmonella serovars are responsible for a majority of human diseases, but nearly all of them belong to subspecies enterica. In a 1995 global survey, serotypes Enteritidis and Typhimurium were the most prevalent serovars of all isolates [60]. The biggest difference among severity and treatment methods is between enteric fever salmonellae and nontyphoid salmonellae (Table 7). It is suggested that a combination of factors specific to each serovar including the presence of plasmid virulence genes (spv), surface cell structure, flagellin, and pathogenity islands (SPIs) is involved in severity of salmonellosis. It has been demonstrated that S. Seftenberg and S. Litchfield have large deletions in invasion related genes, which might have been the result of a selective advantage in the intestinal environment [61]. Jones et al. [62] analyzed data from more than 50 salmonellosis cases from 1996 to 2006 assessing differences among serovars in terms of severity. From these data, most illnesses were related to serovars Typhimurium, Enteritidis, and Newport, while fatality rates reported were in most cases related to serovars Dublin, Muenster, and Choleraesuis.

2.4. Differences among Serovars with respect to Antibiotic Resistance

Resistant Salmonella strains are commonly found in food animal sources [63, 64]. Mismanagement of antimicrobial agents for treatment in humans and animals and the use of growth promoters in livestock have promoted antimicrobial resistance in Salmonellae [64, 65]. The occurrence of Salmonella serovars resistant to quinolones, fluoroquinones, and third generation cephalosporins which are medically significant treatments has increased [66–68]. According to a NARMS report in 2010, the serovars with greater resistance to antimicrobials are Typhimurium specific to ampicillin, chloramphenicol, streptomycin, sulfamethoxazole/sulfisoxazole, and tetracycline (ACSSuT), as well as Enteritidis with resistance to naldixic acid. Serovars Newport, Heidelberg, Dublin, and I4, [5], 12:i:- were also shown to be resistant to various antimicrobial groups (Table 8). In terms of multidrug resistance (more than 5 antimicrobials) the most prevalent serovars of epidemiological importance are Typhimurium, Heidelberg, Dublin, Paratyphi B, and I4, [5], 12:i:- (Table 9). Although S. Enteritidis is highly prevalent in human infections; it has lower antimicrobial resistance compared to other serovars. Antimicrobial resistance in Salmonella can be associated with horizontal transference of antibiotic resistant genes characteristically found on mobile genetic elements among Salmonella strains and other Enterobacteria or by clonal spread of antimicrobial drug resistant serovars that are particularly effective in worldwide dissemination [69–72]. The mechanisms from which Salmonella develops resistance include production of enzymes that can degrade cell permeability to antibiotics, activation of antimicrobial efflux pumps, and production of β-lactamase to degrade the chemical structure of antimicrobial agents [73, 74].

Farm animals have been a common source of isolation for antimicrobial resistant Salmonella serovars [76–78]. A predominantly infectious S. Typhimurium DT104 emerged in the 1980s and has managed to spread worldwide. This serovar commonly carries chromosomally based resistance to five antimicrobials (ACSSuT) and it is believed that it was disseminated worldwide by human travel and then spread locally by the absence of effective antimicrobials [76, 79, 80]. Salmonella Newport has been identified to harbor plasmids encoding ACSSuT and produces β-lactamase, which inactivates cephalosporins, providing resistance to ampicillin and chloramphenicol (AmpC). In human isolates from S. Heidelberg showing high invasive infections, large plasmids (IncA/C and IncI1) were found to carry multiple resistance genes [65, 81]. It is believed that horizontal transmission of virulence genes in multidrug resistant Salmonella strains can increase virulence and invasiveness and cause higher mortality rates compared to susceptible Salmonella [79, 81, 82].

3. Prevalence on the Farm

3.1. Cattle

Salmonellosis in cattle is caused by numerous serovars, with S. Typhimurium and S. Dublin being the most common [83]. Salmonella Dublin serovar is commonly detected in calves and adult cattle. Most infections are introduced into Salmonella free herds by the purchase of infected animals that might have acquired infection on farm premises, in transit or on dealer’s premises [84]. Another route of contamination can be waterborne infection. During the early stages of the acute enteric disease affected animals develop fever, dullness, loss of appetite, and depressed milk yield and adult pregnant animals may abort [83, 85]. Infection of S. Dublin in humans is commonly developed after contact with carrier animals but can also be transmitted through contaminated food and may cause gastroenteritis [86, 87].

In samples taken by FSIS/USDA from 2000 to 2009 from cows and bulls, the increasing prevalence of serovars Montevideo, Newport, Agona, Kentucky, and Mbandanka is notable over the last decade (Table 10). Furthermore, when steers and heifers were submitted to the same testing S. Dublin, S. Montevideo, S. Typhimirium, S. Anatum, and S. Newport were more prevalent than other serovars (Table 11). Beef products are among the top five products related to Salmonella foodborne outbreaks (Table 2). When ground beef was tested, a constant increase in S. Montevideo and S. Dublin isolates was detected from 2004 to 2009, followed by serovars Newport, Typhimurium, and Anatum (Table 12). A multistate sample collection from dairy cows reported that 7.3% of the samples were positive for Salmonella and the five most predominant serotypes were Meleagridis, Montevideo, Typhimurium, Kentucky, and Agona [88]. However, 83% of the isolates were susceptible to all the antimicrobial drugs tested.

3.2. Pigs

Pigs are an important reservoir of human nontyphoidal salmonellosis and the isolation of the organism from pork and pork products is very common. Porcine salmonellae consist of two groups separated by host range and clinical presentation. The first group consists of the host-adapted serovar S. Choleraesuis and tends to elicit systemic disease in the form of septicaemia with a high mortality rate in young pigs. The second group consists of all the other serovars, which have a broader host range and tend to produce momentary enteritis. Like other animal farms, the prevalence of Salmonella from swine varies depending on the region and type of farm surveyed. Prevalence of Salmonella in samples taken from swine farm environments ranges from 3 to 33% [9, 89, 90]. When fecal samples were taken from grower and finisher pigs, the prevalence among serovars was higher for S. Derby and S. Typhimurium followed by Agona and Anatum, which are among the serovars with highest incidence in human foodborne outbreaks [91]. Moreover, 79.6% isolates were resistant to at least one antibiotic [91]. Antimicrobial resistance has been more likely associated with S. Typhimurium and S. Derby and pigs can become asymptomatic carriers [92].

In the US, from 2000 to 2009 the most prevalent serovars isolated from market hogs were Derby, Typhimurium, Johannesburg, Infantis, and Anatum, two of which were also in the top five serotypes isolated from humans in the same period [36]. Other serovars commonly isolated from pigs in recent years include Heidelberg, Saintpaul, and Agona (Table 13). Since the early 1990s there has been a shift in the predominant serovar isolated from swine, where Choleraesuis has a higher incidence and replaced S. Typhimurium.

3.3. Poultry

Chicks may acquire Salmonella via vertical transmission from the parent, but horizontal transmission from environmental facilities, transportation, feed, and vectors including humans, rodents, and insects can be a significant problem [90, 93]. Among commercial layers, contaminated eggs will typically result from flock infections acquired via persistent environmental Salmonella and are associated with the serovar Enteritidis [94–96]. In studies conducted in poultry farms, Salmonella prevalence ranges between 5 and 100% among various environmental and fecal samples [9, 97–99]. It appears that Salmonella Enteritidis filled an ecological niche that was available after eradication of serovars Pullorum and Gallinarum. S. Enteritidis was the most prevalent serovar isolated from chickens during the 1990s but that has changed in the following decade. In recent years the serotypes commonly associated with chickens are Enteritidis, Kentucky, Heidelberg, Typhimurium, and I 4, [5], 12:i:- (Tables 5 and 6).

3.4. Food Products

Salmonella outbreaks linked to consumption of nonmeat foods have rapidly increased during the last decades. Recent data indicates that 13% of the Salmonella outbreaks in the US have been related to contaminated nonmeat foods [100, 101]. Salmonella Saintpaul, S. Rubislaw, and S. Javiana spread by paprika and paprika-powdered potato chips caused outbreaks with more than 1000 infected people [102]. An increase of S. Oranienburg infections was registered in the early 2000s where multistate control studies revealed the consumption of chocolate as the apparent cause of infection [103]. Epidemiological and environmental investigations indicate that cross contamination in the manufacturing plants may be the cause of outbreaks associated with low moisture foods [104]. Salmonella Typhimurium, S. Ofda, S. Tennessee, and S. Poona were isolated from sesame paste and sesame seed which were sold for raw consumption in cereals [105]. It is known that bacteria on plant surfaces may form large biofilms with other bacteria [106]. The persistence of these biofilms makes it difficult to clean and sanitize the crops. These factors are thought to contribute to outbreaks related to plant products including fruits, nuts, and vine stalk vegetables as common sources (Table 3). Outbreaks of salmonellosis associated with seafood that occurred in the US were from cross contamination during farming, processing, preparation, and transportation. From 1999 to 2011, serovars Newport, Typhimurium, Dublin, Montevideo, and Java were reported to have caused outbreaks associated with consumption of milk and cheese products in the US [104]. The reason some Salmonella serovars are more prevalent in specific food products is not completely understood. It is suggested that Salmonellae react in a serovar dependent manner to environmental stresses including differences in temperature, chemicals, and low-nutrient available conditions that can vary by food [107–109].

4. Survival and Stress

4.1. Temperature

Salmonella is considered to be mesophilic with some strains being able to survive at extremely low or high temperatures (2°C to 54°C). Sigma factors are proteins that compose fundamental subunits of prokaryotic RNA polymerase and provide a mechanism for cellular responses by redirecting transcription initiation [110]. Alternate sigma factors control the gene expression of bacteria by sensing the changes in the environment. The sigma factors can sense perturbation in the outer membrane and activate genes in response to heat stress in order to adapt to high temperatures. The mechanism used is by specific activation and transcription of rpoH genes under high temperature [111]. Transcription of rpoH genes in S. Enteritidis was at the highest level when cultured at 42°C. Additionally all virulence genes were upregulated in response to high temperature [112, 113].

Water activity in foods is defined as the ratio of the vapor pressure of water in a food matrix compared to that of pure water at the same temperature. Extended time and temperature are required to kill 90% of Salmonella populations (D-value) in low foods and may reflect the low efficiency of thermal inactivation in dry foods involved in Salmonella related outbreaks including flour, nuts, butter, dry milk, and chocolate [104, 114]. The surrounding moisture and the conformation of the food matrix can influence the thermotolerance of Salmonella by increasing the temperature required to inactivate the organism. Under low conditions in high carbohydrate or high fat products, the heat resistance of S. Seftenberg strain 775W was greater than S. Typhimurium [115–118]. It is widely known that S. Seftenberg strain 775W has high resistance to heat, with a thermotolerance approximately 30 times more than S. Typhimurium. The thermotolerance of Salmonella in poultry products including liquid egg yolks and chicken meat highlights the distinctiveness of S. Seftenberg to survive high cooking temperatures. Other strains of S. Seftenberg and S. Bedford have shown similar inactivation temperatures to strain 775W. Salmonella Senftenberg and S. Typhimurium exhibited higher resistance to heat in chicken litter among other Salmonella serovars [119–121]. Heat stress encountered during feed processing increased the thermotolerance of S. Enteritidis strains and may induce expression of virulence gene hilA in S. Enteritidis, S. Typhimurium, and S. Seftenberg [122, 123]. It is believed that heat resistance confers a preadaptation to temperatures and it is influenced by the strain tested and culture conditions [124, 125].

Salmonella uses cold shock proteins (CSP) as a response for quick adaptation to temperature downshifts in the environment. The CSPs are created during the acclimation phase from 30°C to 10°C. During the downshift CSPs are synthesized for the cell to later resume growth [126–128]. Many studies have been conducted on the ability of salmonellae to increase its survival rate by expressing a CSP when treated at low temperature (5°C to 10°C) prior to freezing. S. Enteritidis was able to survive in chicken parts at 2°C, and in shell eggs at 4°C, while S. Typhimurium survives in minced chicken at 2°C; S. Panama has also shown an elevated propensity to survive in agar at 4°C and S. Typhimurium and S. Tennessee had the ability to survive in estuarine environments below 10°C [129].

4.2. Chemicals

There are a wide variety of potential chemical stresses, including pH, oxidation, membrane disruption, and denaturation of critical macromolecules or metabolic poisons that can affect pathogenic bacteria [130, 131]. Chlorine, commonly used to disinfect water, can be antimicrobial to Salmonella. Salmonellae are capable of producing biofilms providing the organism with an exopolysaccharide matrix that inhibits chemical attack against chlorine [132–134]. Chlorine in recommended doses (2–5 ppm of available chlorine) is able to prevent bacterial biofilm formation in poultry drinking systems and reduce the incidence of Salmonella in the crop and ceca of broilers [135, 136]. However, chlorination by itself is not enough to reduce Salmonella incidence and infection in birds [137].

Decontamination of broiler carcasses occurs during immersion in the chilling tank and the bacterial load in each carcass is expected to be lower than an initial count. The use of chlorine at range of 20–50 ppm in the chilling tank is enough to remove Salmonella biofilm on stainless steel. Chlorine is also used as a sanitizing method in poultry processing plants along with organic acids, inorganic phosphates, and other organic preservatives. Treatments for decontamination of carcasses were performed on different strains of Salmonella in the presence of acidified sodium chlorite varied widely with serotype; the highest resistance levels were shown by serotypes Typhimurium, Newport, and Derby [138]. Among organic acids the use of acetic and propionic acid has shown inhibitory effects against Salmonella [139, 140]. Equipment sanitization is also important, and previous studies have shown the importance of combining sanitizing agents, including detergents and acids. Treatments with sanitizers and detergent successfully inactivated S. Enteritidis cells compared with a 50% inactivation by using sanitizers only [141]. In general, chlorate preparations act as selective toxic agents to enteric pathogens by disrupting cell membrane causing the leakage of intracellular components in bacterium.

4.3. pH

In the case of organic acids their bactericidal activity is related to pH, affecting creation of undissociated acids that will acidify the cytoplasm and disrupt key biochemical processes. In chickens, Salmonella first reaches the crop with a pH range of 4 to 5, as a result of bacterial lactic acid fermentation. If adaptation to that pH occurs, Salmonella can survive and adapt to a more acidic pH and therefore oppose antibacterial effects of the stomach [142].

Many virulence factors in bacteria, including Salmonella, are regulated via the PhoP/PhoQ system. PhoP genes act on the bacterial cell envelope by increasing the resistance to low pH and enhancing survival within the macrophage [143]. Salmonella responds to acidic environmental challenges of pH 5.5 to 6.0 (preshock) followed by exposure of the adapted cells to pH 4.5 (acid shock) and then activates a complex acid tolerance response (ATR) that increases the potential of Salmonella survival under extremely acid environments (pH 3.0 to 4.0) [144]. The ATR mechanism requires acid shock proteins including RpoS sigma factor and PhoPQ. It has been shown that RpoS and PhoPQ provide protection against inorganic acids, while regulators RpoS, iron regulatory protein Fur, and adaptive response protein Ada provide a major tolerance to stress of organic acids [142, 145, 146]. The PhoP locus is a crucial virulence determinant and Salmonella phoP strains are very sensitive to microbial peptides. Several genes, including rpoS, and some acid shock proteins and heat shock proteins are implicated in Salmonella virulence. Commonly isolated from chicken carcasses S. Kentucky shows more acid sensitivity (pH 5.5) than other Salmonella serovars (Enteritidis, Mbandaka, and Typhimurium) [107]. When virulence gene presence was surveyed, acid adaptive stress genes including rpoS, fur, and phoPQ were detected in S. Kentucky [107]. Virulent S. Typhimurium strains with mutations in the rpoS gene were unable to develop a full ATR and had significantly reduced virulence potential [147–149].

It is known that virulence can be activated by acetic acid stress through the hilA gene. Virulence gene expression using hilA in response to pH showed upregulation in strains Typhimurium 23595, Typhimurium 14028, Seftenberg, Heidelberg, Mbandanka, Montevideo, and Infantis [108, 150].

4.4. Desiccation

Salmonella is heat tolerant and persistent in nature and survives long periods of time in dry products but requires for growth. Increasing numbers of multistate Salmonella outbreaks associated with dry foods have occurred [151, 152]. Some of these outbreaks have been characterized by a low infectious dose. It is believed that Salmonella has increased virulence potential induced by survival of other stresses including acid and heat. Salmonellae can be exposed to desiccation stress in the poultry farm environment by numerous factors. Persistence of Salmonella cells in poultry house surroundings, environment dust, dry fecal matter, and floor materials and equipment remaining contaminated after cleaning and sanitization procedures can expose Salmonella to desiccation. The incapacity to detect dormant Salmonella cells may undermine routine hygiene checks [153].

The genetic mechanism of Salmonella survival is related to the proP (Proline permease II) gene. When a proP deletion was assayed, mutants could not survive desiccation for long periods and became undetectable after four weeks. Sigma factor RpoS also plays a role in protecting cells from drying by stabilizing membranes and enzymes by trehalose synthesis, resulting in a more stable structure in the cell [151].

The formation of multicellular filamentous cells by rdar (red, dry, and rough colony) morphology is a major change induced in Salmonella by low exposure. Rdar morphology promotes formation of aggregative fimbriae and cellulose increases desiccation resistance in Salmonella cells, and these can remain viable for months [154, 155]. The of food matrices, product formulation, and storage temperature critically affect the survival of Salmonella in dry food matrices [156]. When bacteria are exposed to desiccation stress, the in the cell is lowered. Strains Enteritidis, Typhimurium, and Mbandaka have been found to have greater persistence (over one year) than Seftenberg, but most authors agree that S. Seftenberg is the most tolerant to desiccation, surviving exposure to detergents and disinfectants up to 30 months [157–159].

More recently a cell shrinkage strategy for Salmonella has been studied as a mechanism of protection during desiccation. A scatter plot analysis showed that the conversion from rod shape to cocci occurred at a greater extent in S. Tennessee (strong desiccation resistance) than S. Typhimurium LT2 (weak desiccation resistance) responding to a 5-day desiccation treatment. Gene expression profile for the two serovars significantly differed with S. Tennessee having no change in genes involved in cell elongation (rodA, rodZ, mrdB, mreB, mrdA, mrcA, and mrcB) after 24 hours of desiccation while S. Typhimurium LT2 cell morphology genes were upregulated from 38- to 91-fold [160].

4.5. Fatty Acid Associated Genes

Adaptive mechanisms of Salmonella related to survival and virulence in low foods include a modification of the fatty acid profile. Salmonella will induce and express genes encoding enzymes involved in the modification of the fatty acids, which will increase osmotolerance.

Increase in cyclopropane fatty acids is considered to be an indicator of starvation or desiccation stress [161]. Fatty acid profiles affect the lipid membrane and increase osmotolerance. Salmonella enterica increases membrane fluidity via fabA, fabB, and cfa pathway [162, 163]. Upregulation of short chain fatty acid related genes including fabA, fabB, and cfa was determined when Salmonella was inoculated in poultry feed [109]. Upregulation of fatty acid catabolic genes has been identified when Salmonella is exposed to dehydration stress under aerobic conditions [151, 164].

4.6. Cross Protection Effects

It is believed that cross protection between different factors including heat and acid stress can affect the virulence of Salmonella, although it is generally acknowledged that several genes, including rpoS, and some acid and heat shock proteins have related effects [148, 165]. For example, desiccation tolerance of Salmonella enterica can have a cross-tolerance effect for other stresses. S. Enteritidis, S. Newport, S. Infantis, and S. Typhimurium can show resistance to commonly used disinfectants, dry heat, and UV irradiation when exposed to a previous dehydration stress. The interaction between temperature and pH is also important. As cross protection effects can impact the survival and virulence of Salmonella, it is important to evaluate these factors during formulation, processing, and preservation of food products.

5. Conclusions

Salmonella serovars are resilient microorganisms with a complex genomic system that makes the organism able to react to different harsh environmental conditions at the farm, during processing and in the gastrointestinal tract. Different stress factors that the bacteria may be exposed to include temperature, pH, osmotic shifts, and low beyond their normal growth range. More research is needed to understand why a few Salmonella serovars are responsible for a majority of human diseases and demonstrate such unique reservoirs and pathogenesis. With a better understanding of serovar specifity, mitigation methods can be implemented to control Salmonella at preharvest and postharvest levels.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

References

P. A. Grimont and F. X. Weill, Antigenic Formulae of the Salmonella Serovars, WHO Collaborating Centre for Reference and Research on Salmonella, Institut Pasteur, Paris, France, 2007.
B. Malorny, E. Hauser, and R. Dieckmann, “New approaches in subspecies-level Salmonella classification,” in Salmonella From Genome to Function, S. Porwollik, Ed., pp. 1–23, Academic Press, Norfolk, UK, 2011.
View at: Google Scholar
B. J. Tindall, P. A. D. Grimont, G. M. Garrity, and J. P. Euzéby, “Nomenclature and taxonomy of the genus Salmonella,” International Journal of Systematic and Evolutionary Microbiology, vol. 55, no. 1, pp. 521–524, 2005.
View at: Publisher Site | Google Scholar
F. W. Brenner, R. G. Villar, F. J. Angulo, R. Tauxe, and B. Swaminathan, “Salmonella nomenclature,” Journal of Clinical Microbiology, vol. 38, no. 7, pp. 2465–2467, 2000.
View at: Google Scholar
A. N. Jensen and J. Hoorfar, “Immediate differentiation of Salmonella-resembling colonies on brilliant green agar,” Journal of Rapid Methods and Automation in Microbiology, vol. 8, no. 3, pp. 219–225, 2000.
View at: Publisher Site | Google Scholar
H. H. Abulreesh, “Salmonellae in the environment,” in Salmonella—Distribution, Adaptation, Control Measures and Molecular Technologies, B. Annous and J. B. Gurtler, Eds., pp. 19–50, InTech, 2012.
View at: Google Scholar
L. Le Minor, “The genus Salmonella,” in The Prokaryotes: A Handbook on the Biology of Bacteria: Ecophysiology, Isolation, Identification, Applications, vol. 1, pp. 2760–2774, Springer, New York, NY, USA, 2nd edition, 1992.
View at: Google Scholar
S. Sanchez, C. L. Hofacre, M. D. Lee, J. J. Maurer, and M. P. Doyle, “Animal sources of salmonellosis in humans,” Journal of the American Veterinary Medical Association, vol. 221, no. 4, pp. 492–497, 2002.
View at: Publisher Site | Google Scholar
A. Rodriguez, P. Pangloli, H. A. Richards, J. R. Mount, and F. A. Draughon, “Prevalence of Salmonella in diverse environmental farm samples,” Journal of Food Protection, vol. 69, no. 11, pp. 2576–2580, 2006.
View at: Google Scholar
K. Hoelzer, A. I. M. Switt, and M. Wiedmann, “Animal contact as a source of human non-typhoidal salmonellosis,” Veterinary Research, vol. 42, no. 1, article 34, 2011.
View at: Publisher Site | Google Scholar
K. E. Sanderson and M. Demerec, “The linkage map of Salmonella typhimurium,” Genetics, vol. 51, pp. 897–913, 1965.
View at: Google Scholar
M. B. Batz, S. Hoffmann, and J. G. Morris Jr., “Ranking the disease burden of 14 pathogens in food sources in the United States using attribution data from outbreak investigations and expert elicitation,” Journal of Food Protection, vol. 75, no. 7, pp. 1278–1291, 2012.
View at: Google Scholar
USDA, “Foodborne illness cost calculator: Salmonella,” 2013, http://www.ers.usda.gov/topics/food-safety/foodborne-illness/salm_intro.asp.
View at: Google Scholar
Center for Disease Control and Prevention (CDC), Foodborne Outbreak Online Database (FOOD), 2013, http://wwwn.cdc.gov/foodborneoutbreaks/Default.aspx.
M. Deligios, D. Bacciu, E. Deriu et al., “Draft genome sequence of the host-restricted Salmonella enterica serovar abortusovis strain SS44,” Genome Announcements, vol. 2, no. 2, Article ID e00261-14, 2014.
View at: Publisher Site | Google Scholar
M. P. McCusker, K. Hokamp, J. F. Buckley, P. G. Wall, M. Martins, and S. Fanning, “Complete genome sequence of Salmonella enterica serovar Agona pulsed-field type SAGOXB.0066, cause of a 2008 Pan-European outbreak,” Genome Announcements, vol. 2, no. 1, pp. e01219-9–e01219-13, 2014.
View at: Publisher Site | Google Scholar
G. Gopinath, J. J.-G. Beaubrun, C. Grim et al., “Whole-genome sequences of six Salmonella enterica Serovar Bovismorbificans isolates associated with a 2011 multistate hummus-borne outbreak,” Genome Announcements, vol. 2, no. 2, 2014.
View at: Publisher Site | Google Scholar
C. H. Chiu, P. Tang, C. Chu et al., “The genome sequence of Salmonella enterica serovar Choleraesuis, a highly invasive and resistant zoonotic pathogen,” Nucleic Acids Research, vol. 33, no. 5, pp. 1690–1698, 2005.
View at: Google Scholar
M. Hoffmann, T. Muruvanda, C. Pirone et al., “First fully closed genome sequence of Salmonella enterica subsp. enterica serovar cubana associated with a food-borne outbreak,” Genome Announcements, vol. 2, no. 5, Article ID e01112-14, 2014.
View at: Publisher Site | Google Scholar
D. A. Russell, C. A. Bowman, and G. F. Hatfull, “Genome sequence of Salmonella enterica subsp. enterica Strain Durban,” Genome Announcements, vol. 2, no. 3, Article ID e00399-14, 2014.
View at: Publisher Site | Google Scholar
N. R. Thomson, D. J. Clayton, D. Windhorst et al., “Comparative genome analysis of Salmonella enteritidis PT4 and Salmonella gallinarum 287/91 provides insights into evolutionary and host adaptation pathways,” Genome Research, vol. 18, no. 10, pp. 1624–1637, 2008.
View at: Publisher Site | Google Scholar
D. Sassera, S. Gaiarsa, E. Scaltriti et al., “Draft genome sequence of Salmonella enterica subsp. enterica serovar Manhattan strain 111113, from an outbreak of human infections in Northern Italy,” Genome Announcements, vol. 1, no. 4, Article ID e00632-13, 2013.
View at: Publisher Site | Google Scholar
E. Barbau-Piednoir, S. Bertrand, N. H. Roosens, and S. C. J. de Keersmaecker, “Genome sequence of the Salmonella enterica subsp. enterica serovar namur strain 05-2929, lacking the Salmonella atypical fimbrial operon,” Genome Announcements, vol. 2, no. 2, Article ID e00299-14, 2014.
View at: Publisher Site | Google Scholar
M. Estrada-Acosta, A. Medrano-Félix, M. Jiménez et al., “Draft genome sequence of Salmonella enterica subsp. enterica serotype saintpaul strain S-70, isolated from an aquatic environment,” Genome Announcements, vol. 1, no. 6, 2013.
View at: Publisher Site | Google Scholar
M. McClelland, K. E. Sanderson, S. W. Clifton et al., “Comparison of genome degradation in Paratyphi A and Typhi, human-restricted serovars of Salmonella enterica that cause typhoid,” Nature Genetics, vol. 36, no. 12, pp. 1268–1274, 2004.
View at: Publisher Site | Google Scholar
A. Medrano-Félix, M. Estrada-Acosta, M. Jimenez et al., “Draft genome sequence of Salmonella enterica subsp. enterica serotype Oranienburg Strain S-76, isolated from an aquatic environment,” Genome Announcements, vol. 1, no. 6, 2013.
View at: Publisher Site | Google Scholar
C. T. Parker, L. Gorski, and S. Huynh, “Complete genome sequence of Salmonella enterica subsp. enterica Serovar Thompson Strain RM6836,” Genome Announcements, vol. 1, no. 6, 2013.
View at: Publisher Site | Google Scholar
J. Parkhill, G. Dougan, K. D. James et al., “Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18,” Nature, vol. 413, no. 6858, pp. 848–852, 2001.
View at: Publisher Site | Google Scholar
M. McClelland, K. E. Sanderson, J. Spieth et al., “Complete genome sequence of Salmonella enterica serovar Typhimurium LT2,” Nature, vol. 413, no. 6858, pp. 852–856, 2001.
View at: Publisher Site | Google Scholar
W. Deng, S.-R. Liou, G. Plunkett III et al., “Comparative genomics of Salmonella enterica serovar Typhi strains Ty2 and CT18,” Journal of Bacteriology, vol. 185, no. 7, pp. 2330–2337, 2003.
View at: Publisher Site | Google Scholar
W. Q. Alali, S. Thakur, R. D. Berghaus, M. P. Martin, and W. A. Gebreyes, “Prevalence and distribution of Salmonella in organic and conventional broiler poultry farms,” Foodborne Pathogens and Disease, vol. 7, no. 11, pp. 1363–1371, 2010.
View at: Publisher Site | Google Scholar
J. S. Bailey, N. J. Stern, P. Fedorka-Cray et al., “Sources and movement of Salmonella through integrated poultry operations: a multistate epidemiological investigation,” Journal of Food Protection, vol. 64, no. 11, pp. 1690–1697, 2001.
View at: Google Scholar
K. G. Maciorowski, F. T. Jones, S. D. Pillai, and S. C. Ricke, “Incidence, sources, and control of foodborne Salmonella spp. in poultry feeds,” World's Poultry Science Journal, vol. 60, no. 4, pp. 446–457, 2004.
View at: Publisher Site | Google Scholar
K. A. Liljebjelke, C. L. Hofacre, T. Liu et al., “Vertical and horizontal transmission of Salmonella within integrated broiler production system,” Foodborne Pathogens and Disease, vol. 2, no. 1, pp. 90–102, 2005.
View at: Publisher Site | Google Scholar
P. Roy, A. S. Dhillon, L. H. Lauerman, D. M. Schaberg, D. Bandli, and S. Johnson, “Results of Salmonella isolation from poultry products, poultry, poultry environment, and other characteristics,” Avian Diseases, vol. 46, no. 1, pp. 17–24, 2002.
View at: Publisher Site | Google Scholar
C. A. Haley, D. A. Dargatz, E. J. Bush, M. M. Erdman, and P. J. Fedorka-Cray, “Salmonella prevalence and antimicrobial susceptibility from the national animal health monitoring system swine 2000 and 2006 studies,” Journal of Food Protection, vol. 75, no. 3, pp. 428–436, 2012.
View at: Publisher Site | Google Scholar
T. W. Hennessy, C. W. Hedberg, L. Slutsker et al., “A national outbreak of Salmonella enteritidis infections from ice cream,” The New England Journal of Medicine, vol. 334, no. 20, pp. 1281–1286, 1996.
View at: Publisher Site | Google Scholar
C. R. Braden, “Salmonella enterica serotype enteritidis and eggs: a national epidemic in the United States,” Clinical Infectious Diseases, vol. 43, no. 4, pp. 512–517, 2006.
View at: Publisher Site | Google Scholar
F. Martelli and R. H. Davies, “Salmonella serovars isolated from table eggs: an overview,” Food Research International, vol. 45, no. 2, pp. 745–754, 2012.
View at: Publisher Site | Google Scholar
D. R. Jones and M. T. Musgrove, “Pathogen prevalence and microbial levels associated with restricted shell eggs,” Journal of Food Protection, vol. 70, no. 9, pp. 2004–2007, 2007.
View at: Google Scholar
Z. R. Howard, C. A. O'Bryan, P. G. Crandall, and S. C. Ricke, “Salmonella Enteritidis in shell eggs:current issues and prospects for control,” Food Research International, vol. 45, no. 2, pp. 755–764, 2012.
View at: Publisher Site | Google Scholar
L. F. Rettger, “Further studies on fatal septicemia in young chickens, or ‘white diarrhea’,” The Journal of Medical Research, vol. 21, no. 1, p. 115, 1909.
View at: Google Scholar
K. L. Bullis, “The history of avian medicine in the U.S. II. Pullorum disease and fowl typhoid,” Avian Diseases, vol. 21, no. 3, pp. 422–429, 1977.
View at: Publisher Site | Google Scholar
S. A. Lister and P. Barrow, “Bacterial diseases,” in Poultry Diseases, M. Pattison, Ed., pp. 110–145, Saunders, Edinburgh, UK, 2008.
View at: Google Scholar
H. M. Hafez and S. Jodas, “Salmonella infections in turkeys,” in Salmonella in Domestic Animals, vol. 1, pp. 133–156, 2000.
View at: Google Scholar
H. L. Shivaprasad, U. Methner, and P. A. Barrow, “Salmonella infections in the domestic fowl,” in Salmonella in Domestic Animals, U. Methner and P. A. Barrow, Eds., pp. 162–192, CABI, Oxfordshire, UK, 2013.
View at: Publisher Site | Google Scholar
H. L. Shivaprasad, “Fowl typhoid and pullorum disease,” Revue Scientifique et Technique de l'OIE, vol. 19, no. 2, pp. 405–424, 2000.
View at: Google Scholar
W. Boyd, “Making meat: science, technology, and American poultry production,” Technology and Culture, vol. 42, no. 4, pp. 631–664, 2001.
View at: Publisher Site | Google Scholar
S. M. L. Kabir, “Avian colibacillosis and salmonellosis: a closer look at epidemiology, pathogenesis, diagnosis, control and public health concerns,” International Journal of Environmental Research and Public Health, vol. 7, no. 1, pp. 89–114, 2010.
View at: Publisher Site | Google Scholar
A. J. Bäumler, B. M. Hargis, and R. M. Tsolis, “Tracing the origins of Salmonella outbreaks,” Science, vol. 287, no. 5450, pp. 50–52, 2000.
View at: Publisher Site | Google Scholar
T. A. Cogan and T. J. Humphrey, “The rise and fall of Salmonella enteritidis in the UK,” Journal of Applied Microbiology, vol. 94, no. 1, pp. 114–119, 2013.
View at: Google Scholar
Y. Kumar, A. Sharma, R. Sehgal, and S. Kumar, “Distribution trends of Salmonella serovars in India (2001–2005),” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 103, no. 4, pp. 390–394, 2009.
View at: Publisher Site | Google Scholar
W. Rabsch, B. M. Hargis, R. M. Tsolis et al., “Competitive exclusion of Salmonella enteritidis by Salmonella gallinarum in poultry,” Emerging Infectious Diseases, vol. 6, no. 5, pp. 443–448, 2000.
View at: Publisher Site | Google Scholar
B. A. Connor and E. Schwartz, “Typhoid and paratyphoid fever in travellers,” The Lancet Infectious Diseases, vol. 5, no. 10, pp. 623–628, 2005.
View at: Publisher Site | Google Scholar
J. A. Crump, P. K. Ram, S. K. Gupta, M. A. Miller, and E. D. Mintz, “Part I. Analysis of data gaps pertaining to Salmonella enterica serotype Typhi infections in low and medium human development index countries, 1984–2005,” Epidemiology and Infection, vol. 136, no. 4, pp. 436–448, 2008.
View at: Publisher Site | Google Scholar
J. A. Crump, S. P. Luby, and E. D. Mintz, “The global burden of typhoid fever,” Bulletin of the World Health Organization, vol. 82, no. 5, pp. 346–353, 2004.
View at: Google Scholar
M. Fangtham and H. Wilde, “Emergence of Salmonella paratyphi A as a major cause of enteric fever: need for early detection, preventive measures, and effective vaccines,” Journal of Travel Medicine, vol. 15, no. 5, pp. 344–350, 2008.
View at: Publisher Site | Google Scholar
W. Rabsch, H. Tschäpe, and A. J. Bäumler, “Non-typhoidal salmonellosis: emerging problems,” Microbes and Infection, vol. 3, no. 3, pp. 237–247, 2001.
View at: Publisher Site | Google Scholar
E. Scallan, R. M. Hoekstra, F. J. Angulo et al., “Foodborne illness acquired in the United States—major pathogens,” Emerging Infectious Diseases, vol. 17, no. 1, pp. 7–15, 2011.
View at: Publisher Site | Google Scholar
H. Herikstad, Y. Motarjemi, and R. V. Tauxe, “Salmonella surveillance: a global survey of public health serotyping,” Epidemiology and Infection, vol. 129, no. 1, pp. 1–8, 2002.
View at: Publisher Site | Google Scholar
C. C. Ginocchio, K. Rahn, R. C. Clarke, and J. E. Galán, “Naturally occurring deletions in the centisome 63 pathogenicity island of environmental isolates of Salmonella spp,” Infection and Immunity, vol. 65, no. 4, pp. 1267–1272, 1997.
View at: Google Scholar
T. F. Jones, L. A. Ingram, P. R. Cieslak et al., “Salmonellosis outcomes differ substantially by serotype,” The Journal of Infectious Diseases, vol. 198, no. 1, pp. 109–114, 2008.
View at: Publisher Site | Google Scholar
M. N. Swartz, “Human diseases caused by foodborne pathogens of animal origin,” Clinical Infectious Diseases, vol. 34, supplement 3, pp. S111–S122, 2002.
View at: Publisher Site | Google Scholar
L.-H. Su, C.-H. Chiu, C. Chu, and J. T. Ou, “Antimicrobial resistance in nontyphoid Salmonella serotypes: a global challenge,” Clinical Infectious Diseases, vol. 39, no. 4, pp. 546–551, 2004.
View at: Publisher Site | Google Scholar
J. Hur, C. Jawale, and J. H. Lee, “Antimicrobial resistance of Salmonella isolated from food animals: a review,” Food Research International, vol. 45, no. 2, pp. 819–830, 2012.
View at: Publisher Site | Google Scholar
G. Rajashekara, E. Haverly, D. A. Halvorson, K. E. Ferris, D. C. Lauer, and K. V. Nagaraja, “Multidrug-resistant Salmonella typhimurium DT104 in poultry,” Journal of Food Protection, vol. 63, no. 2, pp. 155–161, 2000.
View at: Google Scholar
L. J. Martin, M. Fyfe, K. Doré et al., “Increased burden of illness associated with antimicrobial-resistant Salmonella enterica serotype Typhimurium infections,” The Journal of Infectious Diseases, vol. 189, no. 3, pp. 377–384, 2004.
View at: Publisher Site | Google Scholar
M. A. Davis, D. D. Hancock, and T. E. Besser, “Multiresistant clones of Salmonella enterica: the importance of dissemination,” The Journal of Laboratory and Clinical Medicine, vol. 140, no. 3, pp. 135–141, 2002.
View at: Publisher Site | Google Scholar
A. E. Mather, S. W. J. Reid, D. J. Maskell et al., “Distinguishable epidemics of multidrug-resistant Salmonella typhimurium DT104 in different hosts,” Science, vol. 341, no. 6153, pp. 1514–1517, 2013.
View at: Publisher Site | Google Scholar
P. Butaye, G. B. Michael, S. Schwarz, T. J. Barrett, A. Brisabois, and D. G. White, “The clonal spread of multidrug-resistant non-typhi Salmonella serotypes,” Microbes and Infection, vol. 8, no. 7, pp. 1891–1897, 2006.
View at: Publisher Site | Google Scholar
G. B. Michael, P. Butaye, A. Cloeckaert, and S. Schwarz, “Genes and mutations conferring antimicrobial resistance in Salmonella: an update,” Microbes and Infection, vol. 8, no. 7, pp. 1898–1914, 2006.
View at: Publisher Site | Google Scholar
S. D. Alcaine, L. D. Warnick, and M. Wiedmann, “Antimicrobial resistance in nontyphoidal Salmonella,” Journal of Food Protection, vol. 70, no. 3, pp. 780–790, 2007.
View at: Google Scholar
A. M. Sefton, “Mechanisms of antimicrobial resistance,” Drugs, vol. 62, no. 4, pp. 557–566, 2002.
View at: Publisher Site | Google Scholar
S. L. Foley and A. M. Lynne, “Food animal-associated Salmonella challenges: pathogenicity and antimicrobial resistance,” Journal of Animal Science, vol. 86, no. 14, pp. E173–E187, 2008.
View at: Google Scholar
National Antimicrobial Resistance Monitoring System (NARMS), “Executive report,” 2010, http://www.fda.gov/AnimalVeterinary/SafetyHealth/AntimicrobialResistance/NationalAntimicrobialResistanceMonitoringSystem/ucm312356.htm.
View at: Google Scholar
E. F. Dunne, P. D. Fey, P. Kludt et al., “Emergence of domestically acquired ceftriaxone-resistant Salmonella infections associated with AmpC β-lactamase,” The Journal of the American Medical Association, vol. 284, no. 24, pp. 3151–3156, 2000.
View at: Publisher Site | Google Scholar
A. Gupta, J. Fontana, C. Crowe et al., “Emergence of multidrug-resistant Salmonella enterica serotype Newport infections resistant to expanded-spectrum cephalosporins in the United States,” The Journal of Infectious Diseases, vol. 188, no. 11, pp. 1707–1716, 2003.
View at: Publisher Site | Google Scholar
S. Zhao, S. Qaiyumi, S. Friedman et al., “Characterization of Salmonella enterica serotype newport isolated from humans and food animals,” Journal of Clinical Microbiology, vol. 41, no. 12, pp. 5366–5371, 2003.
View at: Publisher Site | Google Scholar
M. K. Glynn, C. Bopp, W. Dewitt, P. Dabney, M. Mokhtar, and F. J. Angulo, “Emergence of multidrug-resistant Salmonella enterica serotype typhimurium DT104 infections in the United States,” The New England Journal of Medicine, vol. 338, no. 19, pp. 1333–1338, 1998.
View at: Publisher Site | Google Scholar
D. Acheson and E. L. Hohmann, “Nontyphoidal salmonellosis,” Clinical Infectious Diseases, vol. 32, no. 2, pp. 263–269, 2001.
View at: Publisher Site | Google Scholar
J. Han, D. E. David, J. Deck et al., “Comparison of Salmonella enterica serovar Heidelberg isolates from human patients with those from animal and food sources,” Journal of Clinical Microbiology, vol. 49, no. 3, pp. 1130–1133, 2011.
View at: Publisher Site | Google Scholar
F. J. Angulo and K. Mølbak, “Human health consequences of antimicrobial drug-resistant Salmonella and other foodborne pathogens,” Clinical Infectious Diseases, vol. 41, no. 11, pp. 1613–1620, 2005.
View at: Publisher Site | Google Scholar
R. la Ragione, H. J. Metcalfe, B. Villarreal-Ramos, D. Werling, P. A. Barrow, and U. Methner, “Salmonella infections in cattle,” in Salmonella in Domestic Animals, pp. 233–262, 2nd edition, 2013.
View at: Publisher Site | Google Scholar
C. Wray, N. Todd, I. McLaren, Y. Beedell, and B. Rowe, “The epidemiology of Salmonella infection of calves: the role of dealers,” Epidemiology and Infection, vol. 105, no. 2, pp. 295–305, 1990.
View at: Publisher Site | Google Scholar
R. F. Kahrs, J. Bentinck-Smith, G. R. Bjorck, D. W. Bruner, J. M. King, and N. F. Lewis, “Epidemiologic investigation of an outbreak of fatal enteritis and abortion associated with dietary change and Salmonella typhimurium infection in a dairy herd. A case report,” The Cornell Veterinarian, vol. 62, no. 2, pp. 175–191, 1972.
View at: Google Scholar
D. L. Fone and R. M. Barker, “Associations between human and farm animal infections with Salmonella typhimurium DT104 in Herefordshire,” Communicable Disease Report. CDR Review, vol. 4, no. 11, pp. R136–140, 1994.
View at: Google Scholar
S. Uzzau, D. J. Brown, T. Wallis et al., “Host adapted serotypes of Salmonella enterica,” Epidemiology and Infection, vol. 125, no. 2, pp. 229–255, 2000.
View at: Publisher Site | Google Scholar
D. M. Blau, B. J. McCluskey, S. R. Ladely et al., “Salmonella in dairy operations in the United States: prevalence and antimicrobial drug susceptibility,” Journal of Food Protection, vol. 68, no. 4, pp. 696–702, 2005.
View at: Google Scholar
R. H. Davies, I. M. McLaren, and S. Bedford, “Observations on the distribution of Salmonella in a pig abattoir,” Veterinary Record, vol. 145, no. 23, pp. 655–661, 1999.
View at: Google Scholar
S. L. Foley, A. M. Lynne, and R. Nayak, “Salmonella challenges: prevalence in swine and poultry and potential pathogenicity of such isolates,” Journal of Animal Science, vol. 86, no. 14, pp. 149–162, 2008.
View at: Google Scholar
USDA/FSIS, “Serotypes Profile of Salmonella Isolates from Meat and Poultry Products January 1998 through December 2011,” 2011, http://www.fsis.usda.gov/wps/portal/fsis/topics/data-collection-and-reports/microbiology/annual-serotyping-reports.
View at: Google Scholar
F. Boyen, F. Haesebrouck, D. Maes, F. van Immerseel, R. Ducatelle, and F. Pasmans, “Non-typhoidal Salmonella infections in pigs: a closer look at epidemiology, pathogenesis and control,” Veterinary Microbiology, vol. 130, no. 1-2, pp. 1–19, 2008.
View at: Publisher Site | Google Scholar
A. Wales, R. H. Davies, P. A. Barrow, and U. Methner, “Environmental aspects of Salmonella,” in Salmonella in Domestic Animals, U. Methner and P. A. Barrow, Eds., pp. 399–425, CABI, Wallingford, UK, 2013.
View at: Google Scholar
A. W. van de Giessen, “Intervention strategies for Salmonella enteritidis in poultry flocks: a basic approach,” International Journal of Food Microbiology, vol. 21, no. 1-2, pp. 145–154, 1994.
View at: Publisher Site | Google Scholar
H. Kinde, D. H. Read, R. P. Chin et al., “Salmonella enteritidis, phage type 4 infection in a commercial layer flock in southern California: bacteriologic and epidemiologic findings,” Avian Diseases, vol. 40, no. 3, pp. 665–671, 1996.
View at: Publisher Site | Google Scholar
A. Wales, M. Breslin, and R. Davies, “Semiquantitative assessment of the distribution of Salmonella in the environment of caged layer flocks,” Journal of Applied Microbiology, vol. 101, no. 2, pp. 309–318, 2006.
View at: Publisher Site | Google Scholar
F. T. Jones, R. C. Axtell, D. V. Rives et al., “A survey of Salmonella contamination in modern broiler production,” Journal of Food Protectection, vol. 54, pp. 502–507, 1991.
View at: Google Scholar
J. J. Carramiñana, J. Yangüela, D. Blanco et al., “Salmonella incidence and distribution of serotypes throughout processing in a Spanish poultry slaughterhouse,” Journal of Food Protection, vol. 60, no. 11, pp. 1312–1317, 1997.
View at: Google Scholar
J. S. Bailey, N. A. Cox, S. E. Craven, and D. E. Cosby, “Serotype tracking of Salmonella through integrated broiler chicken operations,” Journal of Food Protection, vol. 65, no. 5, pp. 742–745, 2002.
View at: Google Scholar
M. P. Doyle and M. C. Erickson, “Reducing the carriage of foodborne pathogens in livestock and poultry,” Poultry Science, vol. 85, no. 6, pp. 960–973, 2006.
View at: Publisher Site | Google Scholar
I. B. Hanning, J. D. Nutt, and S. C. Ricke, “Salmonellosis outbreaks in the united states due to fresh produce: sources and potential intervention measures,” Foodborne Pathogens and Disease, vol. 6, no. 6, pp. 635–648, 2009.
View at: Publisher Site | Google Scholar
A. Lehmacher, J. Bockemuhl, and S. Aleksic, “Nationwide outbreak of human salmonellosis in Germany due to contaminated paprika and paprika-powdered potato chips,” Epidemiology and Infection, vol. 115, no. 3, pp. 501–511, 1995.
View at: Publisher Site | Google Scholar
D. Werber, J. Dreesman, F. Feil et al., “International outbreak of Salmonella Oranienburg due to German chocolate,” BMC Infectious Diseases, vol. 5, no. 1, article 7, 2005.
View at: Publisher Site | Google Scholar
M. P. Doyle and R. L. Buchanan, “Salmonella species,” in Food Microbiology: Fundamentals and Frontiers, pp. 225–261, ASM Press, 4th edition, 2013.
View at: Google Scholar
S. O. Brockmann, I. Piechotowski, and P. Kimmig, “Salmonella in sesame seed products,” Journal of Food Protection, vol. 67, no. 1, pp. 178–180, 2004.
View at: Google Scholar
F. Cooke, E. Threlfall, and J. Wain, “Current trends in the spread and occurrences of human salmonellosis: molecular typing and emerging antibiotic resistance Salmonella,” in Molecular Biology and Pathogenesis, pp. 1–34, 2007.
View at: Google Scholar
R. D. Joerger, C. A. Sartori, and K. E. Kniel, “Comparison of genetic and physiological properties of Salmonella enterica isolates from chickens reveals one major difference between serovar Kentucky and other serovars: response to acid,” Foodborne Pathogens and Disease, vol. 6, no. 4, pp. 503–512, 2009.
View at: Publisher Site | Google Scholar
F. González-Gil, A. Le Bolloch, S. Pendleton, N. Zhang, A. Wallis, and I. Hanning, “Expression of hilA in response to mild acid stress in Salmonella enterica is serovar and strain dependent,” Journal of Food Science, vol. 77, no. 5, pp. M292–M297, 2012.
View at: Publisher Site | Google Scholar
A. Andino, S. Pendleton, N. Zhang, W. Chen, F. Critzer, and I. Hanning, “Survival of Salmonella enterica in poultry feed is strain dependent,” Poultry Science, vol. 93, no. 2, pp. 441–447, 2014.
View at: Publisher Site | Google Scholar
M. J. Kazmierczak, M. Wiedmann, and K. J. Boor, “Alternative sigma factors and their roles in bacterial virulence,” Microbiology and Molecular Biology Reviews, vol. 69, no. 4, pp. 527–543, 2005.
View at: Publisher Site | Google Scholar
M. P. Spector and W. J. Kenyon, “Resistance and survival strategies of Salmonella enterica to environmental stresses,” Food Research International, vol. 45, no. 2, pp. 455–481, 2012.
View at: Publisher Site | Google Scholar
J. H. Brumell, C. M. Rosenberger, G. T. Gotto, S. L. Marcus, and B. B. Finlay, “SifA permits survival and replication of Salmonella typhimurium in murine macrophages,” Cellular Microbiology, vol. 3, no. 2, pp. 75–84, 2001.
View at: Publisher Site | Google Scholar
Y. Yang, W. J. Khoo, Q. Zheng, H.-J. Chung, and H.-G. Yuk, “Growth temperature alters Salmonella enteritidis heat/acid resistance, membrane lipid composition and stress/virulence related gene expression,” International Journal of Food Microbiology, vol. 172, no. 1, pp. 102–109, 2014.
View at: Publisher Site | Google Scholar
V. N. Scott, Y. Chun, J. Kuehm et al., “Control of Salmonella in low-moisture foods I: minimizing entry of Salmonella into a processing facility,” Food Protection Trends, vol. 29, no. 6, pp. 342–353, 2009.
View at: Google Scholar
J. M. Goepfert and R. A. Biggie, “Heat resistance of Salmonella typhimurium and Salmonella senftenberg 775W in milk chocolate,” Applied Microbiology, vol. 16, no. 12, pp. 1939–1940, 1968.
View at: Google Scholar
W. A. Moats, R. Dabbah, and V. M. Edwards, “Survival of Salmonella anatum heated in various media,” Applied Microbiology, vol. 21, no. 3, pp. 476–481, 1971.
View at: Google Scholar
B. Gibson, “The effect of high sugar concentrations on the heat resistance of vegetative micro-organisms,” Journal of Applied Bacteriology, vol. 36, no. 3, pp. 365–376, 1973.
View at: Publisher Site | Google Scholar
K. L. Mattick, F. Jørgensen, P. Wang et al., “Effect of challenge temperature and solute type on heat tolerance of Salmonella serovars at low water activity,” Applied and Environmental Microbiology, vol. 67, no. 9, pp. 4128–4136, 2001.
View at: Publisher Site | Google Scholar
R. Y. Murphy, B. P. Marks, E. R. Johnson, and M. G. Johnson, “Inactivation of Salmonella and Listeria in ground chicken breast meat during thermal processing,” Journal of Food Protection, vol. 62, no. 9, pp. 980–985, 1999.
View at: Google Scholar
M. E. Doyle and A. S. Mazzotta, “Review of studies on the thermal resistance of Salmonellae,” Journal of Food Protection, vol. 63, no. 6, pp. 779–795, 2000.
View at: Google Scholar
Z. Chen, J. Diao, M. Dharmasena, C. Ionita, X. Jiang, and J. Rieck, “Thermal inactivation of desiccation-adapted Salmonella spp. in aged chicken litter,” Applied and Environmental Microbiology, vol. 79, no. 22, pp. 7013–7020, 2013.
View at: Publisher Site | Google Scholar
A. Churi, V. I. Chalova, I. B. Zabala-Díaz, C. L. Woodward, and S. C. Ricke, “Increased temperature influences hilA gene fusion expression in a Salmonella typhimurium poultry isolate,” Food Biotechnology, vol. 24, no. 1, pp. 51–61, 2010.
View at: Publisher Site | Google Scholar
S. H. Park, R. Jarquin, I. Hanning, G. Almeida, and S. C. Ricke, “Detection of Salmonella spp. survival and virulence in poultry feed by targeting the hilA gene,” Journal of Applied Microbiology, vol. 111, no. 2, pp. 426–432, 2011.
View at: Publisher Site | Google Scholar
P. Mañas, R. Pagán, I. Alvarez, and S. C. Usón, “Survival of Salmonella senftenberg 775 W to current liquid whole egg pasteurization treatments,” Food Microbiology, vol. 20, no. 5, pp. 593–600, 2003.
View at: Publisher Site | Google Scholar
D. B. Shah, J. G. Bradshaw, and J. T. Peeler, “Thermal resistance of egg associated epidemic strains of Salmonella enteritidis,” Journal of Food Science, vol. 56, no. 2, pp. 391–393, 1991.
View at: Publisher Site | Google Scholar
A. G. Jeffreys, K. M. Hak, R. J. Steffan, J. W. Foster, and A. K. Bej, “Growth, survival and characterization of CspA in Salmonella enteritidis following cold shock,” Current Microbiology, vol. 36, no. 1, pp. 29–35, 1998.
View at: Publisher Site | Google Scholar
J. E. Craig, D. Boyle, K. P. Francis, and M. P. Gallagher, “Expression of the cold-shock gene cspB in Salmonella typhimurium occurs below a threshold temperature,” Microbiology, vol. 144, no. 3, pp. 697–704, 1998.
View at: Publisher Site | Google Scholar
B. H. Kim, I. S. Bang, S. Y. Lee et al., “Expression of cspH, encoding the cold shock protein in Salmonella enterica serovar Typhimurium UK-1,” Journal of Bacteriology, vol. 183, no. 19, pp. 5580–5588, 2001.
View at: Google Scholar
M. W. Rhodes and H. Kator, “Survival of Escherichia coli and Salmonella spp. in estuarine environments,” Applied and Environmental Microbiology, vol. 54, no. 12, pp. 2902–2907, 1988.
View at: Google Scholar
P. A. Lambert, “Mechanisms of action of biocides. Principles and practice of disinfection,” in Preservation and Sterilization, A. P. Fraise, P. A. Lambert, and J. Y. Maillard, Eds., pp. 139–153, Blackwell, Oxford, UK, 2008.
View at: Google Scholar
A. D. Wales, V. M. Allen, and R. H. Davies, “Chemical treatment of animal feed and water for the control of Salmonella,” Foodborne Pathogens and Disease, vol. 7, no. 1, pp. 3–15, 2010.
View at: Publisher Site | Google Scholar
G. McDonnell and A. D. Russell, “Antiseptics and disinfectants: activity, action, and resistance,” Clinical Microbiology Reviews, vol. 12, no. 1, pp. 147–179, 1999.
View at: Google Scholar
C. Solano, B. García, J. Valle et al., “Genetic analysis of Salmonella enteritidis biofilm formation: critical role of cellulose,” Molecular Microbiology, vol. 43, no. 3, pp. 793–808, 2002.
View at: Publisher Site | Google Scholar
A. P. White and M. G. Surette, “Comparative genetics of the rdar morphotype in Salmonella,” Journal of Bacteriology, vol. 188, no. 24, pp. 8395–8406, 2006.
View at: Publisher Site | Google Scholar
J. A. Byrd, J. R. DeLoach, D. E. Corrier, D. J. Nisbet, and L. H. Stanker, “Evaluation of Salmonella serotype distributions from commercial broiler hatcheries and grower houses,” Avian Diseases, vol. 43, no. 1, pp. 39–47, 1999.
View at: Publisher Site | Google Scholar
L. A. do Amaral, “Drinking water as a risk factor to poultry health,” Revista Brasileira de Ciência Avícola, vol. 6, no. 4, pp. 191–199, 2004.
View at: Publisher Site | Google Scholar
C. Poppe, D. A. Barnum, and W. R. Mitchell, “Effect of chlorination of drinking water on experimental Salmonella infection in poultry,” Avian Diseases, vol. 30, no. 2, pp. 362–369, 1986.
View at: Publisher Site | Google Scholar
R. Capita, “Variation in Salmonella resistance to poultry chemical decontaminants, based on serotype, phage type, and antibiotic resistance patterns,” Journal of Food Protection, vol. 70, no. 8, pp. 1835–1843, 2007.
View at: Google Scholar
K. C. Chung and J. M. Goepfert, “Growth of Salmonella at low pH,” Journal of Food Science, vol. 35, no. 3, pp. 326–328, 1970.
View at: Google Scholar
K. C. Tamblyn and D. E. Conner, “Bactericidal activity of organic acids against Salmonella typhimurium attached to broiler chicken skin,” Journal of Food Protection, vol. 60, no. 6, pp. 629–633, 1997.
View at: Google Scholar
E. A. Zottola and K. C. Sasahara, “Microbial biofilms in the food processing industry—should they be a concern?” International Journal of Food Microbiology, vol. 23, no. 2, pp. 125–148, 1994.
View at: Publisher Site | Google Scholar
I. Rychlik and P. A. Barrow, “Salmonella stress management and its relevance to behaviour during intestinal colonisation and infection,” FEMS Microbiology Reviews, vol. 29, no. 5, pp. 1021–1040, 2005.
View at: Publisher Site | Google Scholar
R. K. Ernst, T. Guina, and S. I. Miller, “How intracellular bacteria survive: surface modifications that promote resistance to host innate immune responses,” The Journal of Infectious Diseases, vol. 179, supplement 2, pp. S326–S330, 1999.
View at: Publisher Site | Google Scholar
A. Álvarez-Ordóñez, M. Prieto, A. Bernardo, C. Hill, and M. López, “The acid tolerance response of Salmonella spp.: an adaptive strategy to survive in stressful environments prevailing in foods and the host,” Food Research International, vol. 45, no. 2, pp. 482–492, 2012.
View at: Publisher Site | Google Scholar
J. W. Foster and H. K. Hall, “Adaptive acidification tolerance response of Salmonella typhimurium,” Journal of Bacteriology, vol. 172, no. 2, pp. 771–778, 1990.
View at: Google Scholar
B. L. Bearson, L. Wilson, and J. W. Foster, “A low pH-inducible, PhoPQ-dependent acid tolerance response protects Salmonella typhimurium against inorganic acid stress,” Journal of Bacteriology, vol. 180, no. 9, pp. 2409–2417, 1998.
View at: Google Scholar
G. J. Leyer and E. A. Johnson, “Acid adaptation induces cross-protection against environmental stresses in Salmonella typhimurium,” Applied and Environmental Microbiology, vol. 59, no. 6, pp. 1842–1847, 1993.
View at: Google Scholar
J. W. Foster and M. P. Spector, “How Salmonella survive against the odds,” Annual Review of Microbiology, vol. 49, no. 1, pp. 145–174, 1995.
View at: Publisher Site | Google Scholar
I. S. Lee, J. Lin, H. K. Hall, B. Bearson, and J. W. Foster, “The stationary-phase sigma factor $σ$ S (RpoS) is required for a sustained acid tolerance response in virulent Salmonella typhimurium,” Molecular Microbiology, vol. 17, no. 1, pp. 155–167, 1995.
View at: Publisher Site | Google Scholar
J. A. Durant, D. E. Corrier, L. H. Stanker, and S. C. Ricke, “Expression of the hilA Salmonella typhimurium gene in a poultry Salm, enteritidis isolate in response to lactate and nutrients,” Journal of Applied Microbiology, vol. 89, no. 1, pp. 63–69, 2000.
View at: Publisher Site | Google Scholar
H. Li, A. Bhaskara, C. Megalis, and M. L. Tortorello, “Transcriptomic analysis of Salmonella desiccation resistance,” Foodborne Pathogens and Disease, vol. 9, no. 12, pp. 1143–1151, 2012.
View at: Publisher Site | Google Scholar
R. Podolak, E. Enache, W. Stone, D. G. Black, and P. H. Elliott, “Sources and risk factors for contamination, survival, persistence, and heat resistance of Salmonella in low-moisture foods,” Journal of Food Protection, vol. 73, no. 10, pp. 1919–1936, 2010.
View at: Google Scholar
L. L. Sarlin, E. T. Barnhart, R. W. Moore, D. E. Corrier, L. H. Stanker, and B. M. Hargis, “Comparison of enrichment methods for recovery and chick infectivity of chlorine-injured Salmonella enteritidis,” Journal of Food Protection, vol. 61, no. 11, pp. 1504–1506, 1998.
View at: Google Scholar
A. P. White, D. L. Gibson, W. Kim, W. W. Kay, and M. G. Surette, “Thin aggregative fimbriae and cellulose enhance long-term survival and persistence of Salmonella,” Journal of Bacteriology, vol. 188, no. 9, pp. 3219–3227, 2006.
View at: Publisher Site | Google Scholar
S. Finn, O. Condell, P. McClure, A. Amézquita, and S. Fanning, “Mechanisms of survival, responses, and sources of Salmonella in low-moisture environments,” Frontiers in Microbiology, vol. 4, article 331, 2013.
View at: Publisher Site | Google Scholar
J. A. Troller, “Water relations of foodborne bacterial pathogens—an updated review,” Journal of Food Protection, vol. 49, no. 1, pp. 656–670, 1986.
View at: Google Scholar
R. H. Davies and C. Wray, “Persistence of Salmonella enteritidis in poultry units and poultry food,” British Poultry Science, vol. 37, no. 3, pp. 589–596, 1996.
View at: Publisher Site | Google Scholar
A. Kumar and S. Kumar, “Survival kinetics of Salmonella enterica serotype senftenberg (S. senftenberg) after heat and acid stress,” World Journal of Microbiology and Biotechnology, vol. 19, no. 9, pp. 985–987, 2003.
View at: Publisher Site | Google Scholar
T. B. Pedersen, J. E. Olsen, and M. Bisgaard, “Persistence of Salmonella Senftenberg in poultry production environments and investigation of its resistance to desiccation,” Avian Pathology, vol. 37, no. 4, pp. 421–427, 2008.
View at: Publisher Site | Google Scholar
C. Megalis, “Cell shrinkage strategy for Salmonella during desiccation,” Unpublished data, 2013.
View at: Google Scholar
T. L. Kieft, D. B. Ringelberg, and D. C. White, “Changes in ester-linked phospholipid fatty acid profiles of subsurface bacteria during starvation and desiccation in a porous medium,” Applied and Environmental Microbiology, vol. 60, no. 9, pp. 3292–3299, 1994.
View at: Google Scholar
C. Baysse and F. O’Gara, “Role of membrane structure during stress signaling and adaptation in Pseudomonas,” in Pseudomonas: A Model System in Biology, J.-L. Ramos and A. Filloux, Eds., pp. 193–224, Springer, Dordrecht, The Netherlands, 2007.
View at: Publisher Site | Google Scholar
B. H. Kim, S. Kim, H. G. Kim, J. Lee, I. S. Lee, and Y. K. Park, “The formation of cyclopropane fatty acids in Salmonella enterica serovar Typhimurium,” Microbiology, vol. 151, no. 1, pp. 209–218, 2005.
View at: Publisher Site | Google Scholar
S. Finn, K. Händler, O. Condell et al., “ProP is required for the survival of desiccated Salmonella enterica serovar typhimurium cells on a stainless steel surface,” Applied and Environmental Microbiology, vol. 79, no. 14, pp. 4376–4384, 2013.
View at: Publisher Site | Google Scholar
G. J. Leyer and E. A. Johnson, “Acid adaptation promotes survival of Salmonella spp. in cheese,” Applied and Environmental Microbiology, vol. 58, no. 6, pp. 2075–2080, 1992.
View at: Google Scholar

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Copyright © 2015 A. Andino and I. Hanning. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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