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Linkages between animal and human health sentinel data

Abstract

Introduction

In order to identify priorities for building integrated surveillance systems that effectively model and predict human risk of zoonotic diseases, there is a need for improved understanding of the practical options for linking surveillance data of animals and humans. We conducted an analysis of the literature and characterized the linkage between animal and human health data. We discuss the findings in relation to zoonotic surveillance and the linkage of human and animal data.

Methods

The Canary Database, an online bibliographic database of animal-sentinel studies was searched and articles were classified according to four linkage categories.

Results

465 studies were identified and assigned to linkage categories involving: descriptive, analytic, molecular, or no human outcomes of human and animal health. Descriptive linkage was the most common, whereby both animal and human health outcomes were presented, but without quantitative linkage between the two. Rarely, analytic linkage was utilized in which animal data was used to quantitatively predict human risk. The other two categories included molecular linkage, and no human outcomes, which present health outcomes in animals but not humans.

Discussion

We found limited use of animal data to quantitatively predict human risk and listed the methods from the literature that performed analytic linkage. The lack of analytic linkage in the literature might not be solely related to technological barriers including access to electronic database, statistical software packages, and Geographical Information System (GIS). Rather, the problem might be from a lack of understanding by researchers of the importance of animal data as a 'sentinel' for human health. Researchers performing zoonotic surveillance should be aware of the value of animal-sentinel approaches for predicting human risk and consider analytic methods for linking animal and human data. Qualitative work needs to be done in order to examine researchers' decisions in linkage strategies between animal and human data.

Introduction

In recent years, there has been increasing awareness on the part of both human and animal health professionals that disease events in animal populations may have direct relevance to human health. As with the analogy of the "canary in the coal mine", animals may serve as sentinels of human health threats in the environment, and work by Halliday and others [1] have focused on establishing a framework to facilitate surveillance efforts. Examples of sentinels include the emergence of zoonotic diseases in wildlife populations concurrent with a novel outbreak of disease in humans such as West Nile Virus (WNV) [2, 3], SARS [4, 5], and Avian Influenza [6, 7]. As a result of these recent events, there has been a heightened emphasis on the use of surveillance efforts in both domestic and wild animal populations. This includes the worldwide surveillance of wild birds for avian influenza. In 2006, the United States Geological Survey, sampled more than 193,000 birds in the US alone as part of their Wild Bird Surveillance Plan [8]. On a global scale, The Global Avian Network for Surveillance (GAINS) surveillance system, funded by US AID, has one of the leading avian surveillance systems and has over 100,000 birds included in their electronic database [9].

This awareness of the shared risk faced by animal and human populations has led to a call for a "One Medicine" approach [10] (now called "One Health"), of communication and interdisciplinary practice between veterinary and human medical professionals. A key part of such an approach is "Joint cross-species disease surveillance and control efforts in public health" (Kahn, L., B. Kaplan, and T.P. Monath: One Health Mission Statement, unpublished). There have been a number of attempts to link human and animal health data such as the tracking of syndromic events in pet animals [11] or the collection of data on sentinel birds for West Nile infection control [12–21]. Controversy exists about the value of such approaches. For example while Eidson et al reported that dead crow clusters predicted human WNV risk [22], Brownstein et al have reported that dead crow sightings are less reliable than mosquito surveillance for prediction of human WNV risk [15]. Similarly, no clear correlations have been published to date from ongoing surveillance of pet populations. Perhaps the clearest example of routine use of animal disease data is in national and state rabies surveillance, in which 49 states and Puerto Rico participated in the monitoring and reporting of nearly 7,000 animal cases (and 3 human cases) to the CDC [23].

Animal health surveillance efforts and human health surveillance efforts are often separate initiatives resulting in the data being stored in separate and potentially vastly different databases. Careful attention and planning must be done if these data sources are to be effectively linked. There is a belief that automated systems to integrate public health data can enhance the surveillance process. The design and development of these systems requires experts in public health informatics, which is the study of the acquisition, storage, and management of electronic public health data for identifying and controlling health issues in the population [24]. Much of the public health informatics work has been in the development of biosurveillance systems that automatically merge disparate health, environmental, geographical, consumer, and population data to model and detect aberrations that might signify a public health priority. Examples include the Real-Time Outbreak and Disease Surveillance Systems (RODS) [25] and the Automated Epidemiologic Geotemporal Integrated Surveillance Systems (AEGIS) [26] that use electronic hospital syndromic information to predict bioterrorism and naturally occurring outbreaks such as influenza.

In order to identify priorities for building integrated surveillance systems that effectively model and predict human risk of zoonotic disease, there is a need for improved understanding of the practical options for linking surveillance data of animals and humans. For this study, we performed an analysis of the Canary Database [27], an online resource for literature on the animal-sentinel interface, in order to examine the use of how animal and human data is linked for analysis purposes. The Canary Database does not represent the entire spectrum of epidemiological papers of animal-human events. However, the purpose of this paper is not an exhaustive search of the literature on animal-human health events. Rather, the intent is to highlight the use of various linkage strategies for animal and human data and discuss implications of these strategies for public health research. In addition, both humans and non-human animals share the same ecosystem and while it is possible that animals can serve as sentinels for humans, there are times when a sentinel event in humans has implications for animal health. The Canary Database, however, is oriented toward animals as sentinels for human health hazards, therefore for the remainder of this paper, we use the term 'animal sentinel' to mean an instance in which a non-human animal might indicate concurrent or future health risk to humans. However, we believe that our findings regarding linkage between human and animal data streams have relevance to both human health and animal health.

Methods

The Canary Database [27] is a publicly accessible online database of studies in the biomedical literature concerned with animals as sentinels of zoonotic, environmental, and toxic effects on human health. Curators of this database include both human and animal health professionals who periodically search the medical bibliographic databases such as PubMed and identify, using predetermined algorithms, studies that analyze the effects of zoonotic and environmental health hazards on free ranging animal populations, including companion, livestock, and wildlife animals. Articles are curated into the database according to study methodology, hazards and outcomes studied, animal species, and location. Currently, there are over 1,600 articles in the database going back to 1966.

Using the advanced search feature in the Canary Database, an initial group of papers were retrieved that described at least a shared health outcome between animals and humans or a shared exposure (e.g. of an environmental toxin). Then, two of the reviewers (MS and LO) reviewed the curated information for each of these papers and if needed, the papers themselves, to determine if they were original investigations. Review articles and media analysis (newspaper or magazine articles) were not included. In addition, papers describing laboratory-based toxicology work were not included.

For each paper in the study, we defined their linkage category, based on consensus among the authors, to be at least one of four possibilities:

â—¦ Analytic: Studies that use quantitative methods to assess human risk. For example, studies that use cases of WNV found in dead crows to quantify the risk of the disease in humans, would fall under this category.

â—¦ Descriptive: Studies that describe the health outcomes in both animals and humans, but do not attempt a quantitative linkage between the two. For example, a seroprevalence study that lists the number of positive Hantavirus cases in both rodents and humans in a particular area would fall under this category.

â—¦ Molecular: Studies in which the investigators use molecular epidemiological techniques to show similarities between strains of a pathogen occurring in animals compared to humans, thereby providing evidence as to whether or not species crossover of infection has occurred. For example, studies that use phylogenetic algorithms to assess the lineage of H5N1 Avian Influenza strains isolated in animals and humans would fall under this category.

â—¦ No human outcomes. Studies in which no outcomes in humans are considered. These studies often provide evidence of exposure in humans, but do not discuss outcomes related to human health. For example, a study that assesses the bioaccumulation of mercury in tilapia would fall under this category. Humans are considered exposed since they could eat the fish or drink the contaminated water but outcomes are not assessed.

Thus, the first three categories represent original investigations that describe health outcomes in both animals and humans, while the final category describes all papers that include only animal outcomes or no health outcomes at all.

Each paper was assigned to at least one of these four linkage categories, with some papers counted in two categories. For example a paper that describes the seroprevalence of a field study of Nipah Virus in fruit bats and humans and then develops a phylogenetic tree to assess the similarities would be considered both a descriptive linkage and a molecular linkage.

Results

At the time of this study, Canary contained 1,661 articles from 1966 to 2007. Of these, 465 (28%) were judged to be appropriate original epidemiological investigations that related animal disease data to human disease data. These 465 papers were further analyzed.

Table 1 shows that the majority of studies linked animal and human data in a descriptive fashion (57%), thus describing or listing the number of cases in animals and humans without an attempt to predict future risk based on the results. This often includes the trapping of suspected animal reservoirs that are located in the vicinity of confirmed or suspected human cases. In these types of studies, results are often reported as percentage of positive cases in animals and percentage of positive cases in humans. Complicated or in-depth statistical analysis is often not conducted in descriptive linkage studies. Papers that used analytic methods ([2, 13, 15, 18, 20, 21, 28–50]) to link animal and human data consisted of 6% of the articles retrieved and the methods used in each are summarized in Table 2. For each paper, the primary author, the zoonotic disease, the animals studied (domestic, livestock, or wildlife), and our summary of the methods for analytic linkage are presented.

Table 1 Papers in our Canary search by type of Linkage Category.
Table 2 Papers in our Canary search using Analytic Linkage for human and animal health data

Analytic Linkage of Human and Animal Data Using Regression

Popular linkage approaches included multiple regression (Logistic, Linear, Poisson), spatial analysis (Cluster analysis, Digital mapping, etc.) and odds ratio/relative risk calculation. The purpose of these papers tended to use infection, death, or contact with animals as the main independent variable to predict risk of infection in humans. Many also used additional input variables such as interview and survey data to identify the most parsimonious model. For example a paper by Dubey et al [30] studying risk of Toxoplasmosis on US farms collected interview data from farmers and collected blood and fecal specimens from animals and farmers as well as soil and water samples. In order to study the association between the seroprevalence of farmers, the authors combined the various animal specimen data with farmer interview data in a logistic regression model. Seroprevalence of toxoplasmosis in cats was the only variable found to be significant. In another study, Brownstein et al [15] used a regression model to study the value of non-human surveillance programs on predicting risk in humans. The authors used data from the ArboNet system such as number of virus-positive birds, mosquitoes and humans and evaluated the models predictive ability by assessing the coefficient of determination (R2) [15].

Analytic Linkage of Human and Animal Data Using Spatial Analysis

Many of the articles used spatial analysis in which georeferenced locations of infected cases or reported animal deaths were considered. This demonstrates the growing interest by epidemiologists and animal health researchers in examining spatial factors in relation to animal and human health monitoring. For example, the spatial scan statistic, developed by Kulldorff [51], has been widely used to identify disease clusters. The statistic scans temporal or spatial data, calculates the number of observed and expected observations (infections, deaths, etc.) using a shape (for spatial analysis) such as a circle or ellipse or an interval (for temporal analysis). The method then uses the likelihood ratio test to determine if the area inside the shape is significantly different than the outside area [51, 52]. Statistical significance of the cluster with the maximum likelihood is then assessed by Monte Carlo simulation testing. Many of the analytic linkage papers used spatial scan functions to identify clusters of events such as animal deaths or infected cases of humans or animals. For example, Brownstein et al. [29] studied vegetation index data as a means to identify clusters of West Nile Virus in mosquitoes in New York City in 1999 [29]. The authors obtained human case information for New York City in 1999 from the local health department, a census track boundary map and population data from the US Census Bureau, and vegetation data from a United States Geological Survey (USGS) Landsat image [29]. Kulldorff's spatial scan statistic using a Poisson distribution model was used to detect clusters of West Nile. Once the clusters were detected, the authors used ANOVA to examine whether Normalized Difference Vegetation Index (NDVI) differed between clusters and non-clusters and used Logistic regression to determine if NDVI could identify census tracks within clusters that had cases of WNV. The authors concluded that mosquito and vegetation data, in conjunction with the spatial analysis might provide early evidence of human WNV risk [29].

Analytic Linkage of Human and Animal Data Using Mathematical Modeling

Another analytic linkage method for animal and human data we found was mathematical modeling. Many researchers use dynamic stochastic models in which simulated data based on various distributions is represented as differential equations. For example, Li et al [36] used a probability model to examine the relationship between sentinel animals for transmission of arboviruses. As part of their work, the authors examined the relationship between various levels of vector bites per host per season and the mean number of human cases of an arbovirus [36]. Other calculated parameters in their model included "vector infection rate" ([36], pg. 450), "probability of an animal or human host becoming infected" ([36], pg. 450) and "the number of seroconverted samples on each sampling date" ([36], pg. 450). The authors concluded that human risk is "negatively related to the distance from the vector epicenter" ([36], pg. 450). These models can then be used as a means to predict risk of human infection given actual ecological data.

Analytic Linkage of Human and Animal Data Using Risk Ratios

Several of the papers that used analytic linkage of animal and human data used direct calculation of risk ratios such as relative risk and odds ratios. These can often be calculated directly using contingency tables. The ratios are often used in active surveillance studies where the number of observations and variables collected is relatively small. For example Mannelli et al [37] calculated relative risk to determine the association between occupation and exposure to tick bites for Lyme Disease, while Gurtler et al [33] calculated the relative risk for the combined effect of T. cruzi in dogs and children and infected Triatoma infestans (insects). The authors performed a house-to-house survey and performed laboratory analysis on all household members, dogs, and Triatoma infestans. They determined that a causal association existed between the presence of infected dogs and infected insects [33].

Analytic Linkage of Human and Animal Data Using Cross Correlation Functions

Cross-correlation function (CCF) has been used as a method to identify leading indicators of disease outbreaks [53]. The emphasis here is to examine the relationship between time series [53] to determine the lead-lag correlation. CCF have been widely used to examine various financial indices and the fluctuations in the stock market [54]. Two of the papers in the Canary Database that use analytic linkage used the cross-correlation function. In Niklasson et al [42], the authors used CCF to examine the relationship between human hantavirus infection and vole density. The authors concluded that in the Fall months, there was more of a concurrent relationship between vole density and human infection, whereas in the Spring, human infection was dependent on the density in the preceding Fall months [42]. In this Swedish epidemiological study, the authors utilized national incidence data from 1985–1992 and trapping of voles [42].

Discussion

Examples of public health scenarios in which animal data can be used to inform decision making include:

  1. 1.

    Linkage of surveillance data streams through reporting of companion, livestock, or wildlife populations in order to gauge human risk.

  2. 2.

    Surveys of animal reservoirs to support a specific human outbreak investigation.

  3. 3.

    Surveys of animal reservoirs in the absence of a known human outbreak to gauge human risk and determine the need for public health and animal control measures.

  4. 4.

    Short-term surveys of unusual clusters of disease in animals that can lead to hypothesis about human risk.

  5. 5.

    Intentional sentinels (captive chickens, cows, etc.) followed in a cohort fashion to gauge increase or decrease in human risk.

  6. 6.

    Analysis and comparison of available human and animal isolates of an infectious agent to monitor genetic shifts in infectious agents.

Scenario 1 involves domestic or livestock animal medical cases by veterinarians or general public reporting of wildlife (such as dead birds). The animal health data in this scenario is reported to agencies such as the Departments of Agriculture, Wildlife, or Public Health. Many of these involve cases of suspected reportable animal diseases to the Department of Agriculture or public sightings of dead birds to the Department of Wildlife or Department of Health. An example is the use of dead crow sightings for West Nile Virus surveillance [20].

Scenario 2 involves outbreak investigation of human cases by obtaining health data on animals. The majority of disease surveillance in wildlife is short-term and often in response to known cases or spread of the disease [55]. This generally involves trapping, seroprevalence, and necropsy of wildlife in the vicinity of the human cases. It might also involve the testing of domestic animals in the belief of pet-owner transmission. These surveys are often initiated by governmental agencies such as the Department of Agriculture, Wildlife, or Public Health. An example is the investigation of anthrax in cattle and sheep on numerous Australian farms [56].

Scenario 3 is short or long-term seroprevalence surveys, typically of wildlife animals, to estimate the degree of infection of a specific zoonotic disease in animals. These surveys can be initiated by governmental agencies or also the result of independent research by university scientists. Trapping and testing rodents for plague in a country in order to estimate the levels of infection in wildlife is an example of this scenario [57].

Scenario 4 is similar to scenario 2, but is initiated by the discovery of unusual animal deaths, not human deaths.

Scenario 5 involves the use of specific sentinel animals (generally livestock) for long-term assessment of infection rates. An example is the use of sentinel chickens and horses for West Nile virus assessment as part of the ArboNET surveillance program [58].

Scenario 6 differs from the other scenarios because of its emphasis on laboratory techniques in the domain of molecular epidemiology. The intention is to examine similarities between strains of a pathogen occurring in animals compared to humans, thereby providing evidence as to whether or not species crossover of infection has occurred. An example is the development of phylogenetic trees to examine similarities between animal and human strains of Hantavirus [59].

In our analysis, descriptive linkage was the most common linkage category found. The use of animal data to quantitatively predict risk in human was limited. This lack of analytic linkage can impact the development of automated public health informatics systems to support surveillance. Analytic linkage is inherent in early warning surveillance systems for predicting risk in humans based on a range of variables (syndromes, animals, behavior, environment, etc.). For example, value has been shown in the use of dead crows and infected mosquitoes for predicting human risk of West Nile Virus [2, 15, 20, 22]. Without this evidence, it is likely that much less funding would go into development of early warning WNV systems that link animal and human data. A lack of analytic linkage will produce a lack of scientific merit for using animals as sentinels for estimating human risk. This is a global problem as noted by Childs, that "as of 2006, there appears to be little scientific, social, or political consensus that animal-based surveillance for zoonoses merits investment in international infrastructure." pg. 423 [55]. The author does note that recent collaborations by the World Health Organization (WHO), Food and Agricultural Organization (FAO), and the World Organization for Animal Health (OIE), to develop GLEWS, an integrated early-warning system, might signal a change in the right direction [55].

In addition descriptive linkage is suitable for public health researchers looking at discrete events, but it can get overwhelming if there is too much data. The reliance on descriptive linkage puts a burden on public health users and also creates discrepancies in how different users interpret the results. For example, as more governmental money has gone into the epidemiology of Highly Pathogenic Avian Influenza (HPAI), many studies have been initiated and large amounts of data have been generated. However, the onus is on the researcher to analyze the descriptive data across all of these studies and draw conclusions without the aid of analytic methods for linking the findings. Interpretation of the data determines if public health control measures should be implemented. For zoonoses outbreaks, these measures can carry significant financial consequences such as the slaughtering of animals, and the cessation of trade.

We believe the three scenarios that tend to have long-term data collection (1, 3, and 5) benefit most from the use of analytic linkage between human and animal data. For example, scenario 1 is a long-term focus with passive data collection that relies on the motivation of veterinarians or the general public to report suspected cases. Scenario 1 is well suited for public health informatics systems that transfer, manage, and analyze longitudinal case data. The collection of cases over many years allows for analytic linkage of human and animal data through temporal and geographical comparisons. However, the lack of integrated informatics systems at animal and human agencies makes analysis of longitudinal health and animal data difficult. Animal and human agencies that do not use these systems to manage their case data make it difficult to integrate animal and human health data and conduct quantitative linkage. While it is encouraging that large numbers of papers have attempted to look at linking animal and human data, more emphases needs to be in quantitatively linking animal and human data. This will provide more scientific merit that animal data can be used as sentinels for predicting human risk, and hopefully promote the need for public health informatics surveillance systems to automatically integrate the animal and human data. In addition, the importance of the "One Medicine" [10] (or "One Health") collaboration needs to be emphasized across veterinary and human medicine through formal education, conferences and workshops, journal articles, and professional collaborations. An acceptance and belief of one medicine will heighten the recognition for using animal health data as a sentinel for determining risk in humans. It will also emphasize the importance of quantitative linkage between the two domains for producing empirical scientific evidence that will serve to strengthen this initiative and the development of automated animal-human informatics systems.

In our review of the Canary Database, we found different strategies for analytic linkage including: multivariate regression, direct calculation of risk ratios, spatial analysis including scan statistics, cross-correlation functions, and mathematical modeling. There are many other methods that were not found that might also be useful for analytic linkage of animal and human data. Other surveillance approaches include Bayesian Networks, rule-based analysis, and various time-series methods [60]. The authors here are not advocating one linkage approach over another. Each situation is different depending on the study goals, the prevalence of the disease in the area, additional variables collected, the number of observations, how many years of data were collected, and access to statistical and spatial software. It is possible that the key barrier to analytic linkage is not technological, but rather the lack of understanding of researchers of the importance of animal data as a 'sentinel' for human health. Our study highlighted that lack of animal-sentinel approaches in epidemiology and listed methods from the literature for performing these types of linkages. Researchers performing zoonotic surveillance should be aware of the value of animal-sentinel approaches for predicting human risk and consider analytic methods for linking animal and human data. Table 2 lists examples of Arboviruses such as West Nile Virus that use analytic linkage. As variables such as crow mortality and mosquito abundance have shown to be valuable for empirically predicting human risk, follow-up studies using additional data sources and analytic linkage efforts have been performed. As other research initiatives in public health provide empirical evidence for animal-sentinel surveillance, more scientific work that uses analytic methods to link this information will be performed. Finally, efforts such as the One Health Initiative [61], which focus on the collaboration of human and animal medicine, represent important collaborations to address this lack of recognition between the value of animal-human linkage. Going forward, qualitative work needs to be done in order to examine researchers' decisions in linkage strategies between animal and human surveillance data.

Limitations

While the Canary Database is not an exhaustive compilation of all scientific studies relevant to issues of animal sentinels for human health risk, it does represent a systematic attempt to sample the published scientific literature from 1966 to 2007 to identify such studies. It therefore was a reasonable sample to use for this attempt to characterize the nature of epidemiological linkages between human and animal health data related to environmental exposure risks.

References

  1. Halliday JE, Meredith AL, Knobel DL, Shaw DJ, Bronsvoort BM, Cleaveland S: A framework for evaluating animals as sentinels for infectious disease surveillance. J R Soc Interface. 2007, 4 (16): 973-984.

    Article  PubMed Central  PubMed  Google Scholar 

  2. Watson JT, Jones RC, Gibbs K, Paul W: Dead crow reports and location of human West Nile virus cases, Chicago, 2002. Emerg Infect Dis. 2004, 10 (5): 938-940.

    Article  PubMed Central  PubMed  Google Scholar 

  3. O'Leary DR, Marfin AA, Montgomery SP, Kipp AM, Lehman JA, Biggerstaff BJ, Elko VL, Collins PD, Jones JE, Campbell GL: The epidemic of West Nile virus in the United States, 2002. Vector Borne Zoonotic Dis. 2004, 4 (1): 61-70.

    Article  PubMed  Google Scholar 

  4. Wang M, Yan M, Xu H, Liang W, Kan B, Zheng B, Chen H, Zheng H, Xu Y, Zhang E, et al: SARS-CoV infection in a restaurant from palm civet. Emerg Infect Dis. 2005, 11 (12): 1860-1865.

    Article  PubMed Central  PubMed  Google Scholar 

  5. Ng SK: Possible role of an animal vector in the SARS outbreak at Amoy Gardens. Lancet. 2003, 362 (9383): 570-572.

    Article  PubMed  Google Scholar 

  6. Shortridge KF, Zhou NN, Guan Y, Gao P, Ito T, Kawaoka Y, Kodihalli S, Krauss S, Markwell D, Murti KG, et al: Characterization of avian H5N1 influenza viruses from poultry in Hong Kong. Virology. 1998, 252 (2): 331-342.

    Article  CAS  PubMed  Google Scholar 

  7. Sims LD, Ellis TM, Liu KK, Dyrting K, Wong H, Peiris M, Guan Y, Shortridge KF: Avian influenza in Hong Kong 1997–2002. Avian Dis. 2003, 47 (3 Suppl): 832-838.

    Article  CAS  PubMed  Google Scholar 

  8. Anonymous: Avian Influenza Surveillance of Wild Birds. USGS Fact Sheet. 2007, 3094:

    Google Scholar 

  9. Hively E: Wild Bird GAINS: Global Avian Influenza Network for Surveillance of Wild Birds. GAINS Fact Sheet. 2007.

    Google Scholar 

  10. Schwabe CW: Veterinary medicine and human health. Baltimore: Williams & Wilkins; 1984. 3

    Google Scholar 

  11. Glickman LT, Moore GE, Glickman NW, Caldanaro RJ, Aucoin D, Lewis HB: Purdue University-Banfield National Companion Animal Surveillance Program for emerging and zoonotic diseases. Vector Borne Zoonotic Dis. 2006, 6 (1): 14-23.

    Article  PubMed  Google Scholar 

  12. Hadler J, Nelson R, McCarthy T, Andreadis T, Lis MJ, French R, Beckwith W, Mayo D, Archambault G, Cartter M: West Nile virus surveillance in Connecticut in 2000: an intense epizootic without high risk for severe human disease. Emerg Infect Dis. 2001, 7 (4): 636-642.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Andreadis TG, Anderson JF, Vossbrinck CR, Main AJ: Epidemiology of West Nile virus in Connecticut: a five-year analysis of mosquito data 1999–2003. Vector Borne Zoonotic Dis. 2004, 4 (4): 360-378.

    Article  PubMed  Google Scholar 

  14. Blackmore CG, Stark LM, Jeter WC, Oliveri RL, Brooks RG, Conti LA, Wiersma ST: Surveillance results from the first West Nile virus transmission season in Florida, 2001. Am J Trop Med Hyg. 2003, 69 (2): 141-150.

    PubMed  Google Scholar 

  15. Brownstein JS, Holford TR, Fish D: Enhancing West Nile virus surveillance, United States. Emerg Infect Dis. 2004, 10 (6): 1129-1133.

    Article  PubMed Central  PubMed  Google Scholar 

  16. Cernescu C, Nedelcu NI, Tardei G, Ruta S, Tsai TF: Continued transmission of West Nile virus to humans in southeastern Romania, 1997–1998. J Infect Dis. 2000, 181 (2): 710-712.

    Article  CAS  PubMed  Google Scholar 

  17. Cherry B, Trock SC, Glaser A, Kramer L, Ebel GD, Glaser C, Miller JR: Sentinel chickens as a surveillance tool for West Nile virus in New York City, 2000. Ann N Y Acad Sci. 2001, 951: 343-346.

    Article  CAS  PubMed  Google Scholar 

  18. Corrigan RL, Waldner C, Epp T, Wright J, Whitehead SM, Bangura H, Young E, Townsend HG: Prediction of human cases of West Nile virus by equine cases, Saskatchewan, Canada, 2003. Prev Vet Med. 2006, 76 (3–4): 263-272.

    Article  PubMed  Google Scholar 

  19. Dietrich G, Montenieri JA, Panella NA, Langevin S, Lasater SE, Klenk K, Kile JC, Komar N: Serologic evidence of west nile virus infection in free-ranging mammals, Slidell, Louisiana, 2002. Vector Borne Zoonotic Dis. 2005, 5 (3): 288-292.

    Article  PubMed  Google Scholar 

  20. Eidson M, Miller J, Kramer L, Cherry B, Hagiwara Y: Dead crow densities and human cases of West Nile virus, New York State, 2000. Emerg Infect Dis. 2001, 7 (4): 662-664.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Guptill SC, Julian KG, Campbell GL, Price SD, Marfin AA: Early-season avian deaths from West Nile virus as warnings of human infection. Emerg Infect Dis. 2003, 9 (4): 483-484.

    Article  PubMed Central  PubMed  Google Scholar 

  22. Eidson M, Kramer L, Stone W, Hagiwara Y, Schmit K: Dead bird surveillance as an early warning system for West Nile virus. Emerg Infect Dis. 2001, 7 (4): 631-635.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  23. Blanton JD, Hanlon CA, Rupprecht CE: Rabies surveillance in the United States during 2006. J Am Vet Med Assoc. 2007, 231 (4): 540-556.

    Article  PubMed  Google Scholar 

  24. O'Carroll PW: Public health informatics and information systems. New York: Springer; 2002.

    Google Scholar 

  25. Tsui FC, Espino JU, Dato VM, Gesteland PH, Hutman J, Wagner MM: Technical description of RODS: a real-time public health surveillance system. J Am Med Inform Assoc. 2003, 10 (5): 399-408.

    Article  PubMed Central  PubMed  Google Scholar 

  26. Reis BY, Kirby C, Hadden LE, Olson K, McMurry AJ, Daniel JB, Mandl KD: AEGIS: a robust and scalable real-time public health surveillance system. J Am Med Inform Assoc. 2007, 14 (5): 581-588.

    Article  PubMed Central  PubMed  Google Scholar 

  27. Wiley JDJF, Gordon ZJ, Odofin LU, Rabinowitz PM: The canary database: Animals as sentinels of human environmental health hazards. Clinical Toxicology. 2005, 43 (6): 720-

    Google Scholar 

  28. Ascione FR, Weber CV, Thompson TM, Heath J, Maruyama M, Hayashi K: Battered pets and domestic violence: animal abuse reported by women experiencing intimate violence and by nonabused women. Violence Against Women. 2007, 13 (4): 354-373.

    Article  PubMed  Google Scholar 

  29. Brownstein JS, Rosen H, Purdy D, Miller JR, Merlino M, Mostashari F, Fish D: Spatial analysis of West Nile virus: rapid risk assessment of an introduced vector-borne zoonosis. Vector Borne Zoonotic Dis. 2002, 2 (3): 157-164.

    Article  PubMed  Google Scholar 

  30. Dubey JP, Weigel RM: Epidemiology of Toxoplasma gondii in farm ecosystems. J Eukaryot Microbiol. 1996, 43 (5): 124S-

    Article  CAS  PubMed  Google Scholar 

  31. Ezenwa VO, Godsey MS, King RJ, Guptill SC: Avian diversity and West Nile virus: testing associations between biodiversity and infectious disease risk. Proc Biol Sci. 2006, 273 (1582): 109-117.

    Article  PubMed Central  PubMed  Google Scholar 

  32. Ferguson NM, Ghani AC, Donnelly CA, Hagenaars TJ, Anderson RM: Estimating the human health risk from possible BSE infection of the British sheep flock. Nature. 2002, 415 (6870): 420-424.

    Article  CAS  PubMed  Google Scholar 

  33. Gurtler RE, Cecere MC, Rubel DN, Petersen RM, Schweigmann NJ, Lauricella MA, Bujas MA, Segura EL, Wisnivesky-Colli C: Chagas disease in north-west Argentina: infected dogs as a risk factor for the domestic transmission of Trypanosoma cruzi. Trans R Soc Trop Med Hyg. 1991, 85 (6): 741-745.

    Article  CAS  PubMed  Google Scholar 

  34. Julian KG, Eidson M, Kipp AM, Weiss E, Petersen LR, Miller JR, Hinten SR, Marfin AA: Early season crow mortality as a sentinel for West Nile virus disease in humans, northeastern United States. Vector Borne Zoonotic Dis. 2002, 2 (3): 145-155.

    Article  PubMed  Google Scholar 

  35. Keeling MJ, Gilligan CA: Metapopulation dynamics of bubonic plague. Nature. 2000, 407 (6806): 903-906.

    Article  CAS  PubMed  Google Scholar 

  36. Li X, Rossignol PA: Probability model on the use of sentinel animal monitoring for arbovirus. Epidemiology. 1998, 9 (4): 446-451.

    Article  CAS  PubMed  Google Scholar 

  37. Mannelli A, Cerri D, Buffrini L, Rossi S, Rosati S, Arata T, Innocenti M, Grignolo MC, Bianchi G, Iori A, et al: Low risk of Lyme borreliosis in a protected area on the Tyrrhenian coast, in central Italy. Eur J Epidemiol. 1999, 15 (4): 371-377.

    Article  CAS  PubMed  Google Scholar 

  38. Mannelli A, Mandola ML, Pedri P, Tripoli M, Nebbia P: Associations between dogs that were serologically positive for Rickettsia conorii relative to the residences of two human cases of Mediterranean spotted fever in Piemonte (Italy). Prev Vet Med. 2003, 60 (1): 13-26.

    Article  CAS  PubMed  Google Scholar 

  39. Marrie TJ, Durant H, Williams JC, Mintz E, Waag DM: Exposure to parturient cats: a risk factor for acquisition of Q fever in Maritime Canada. J Infect Dis. 1988, 158 (1): 101-108.

    Article  CAS  PubMed  Google Scholar 

  40. Mitra M, Mahanta SK, Sen S, Ghosh C, Hati AK: Sarcoptes scabiei in animals spreading to man. Trop Geogr Med. 1993, 45 (3): 142-143.

    CAS  PubMed  Google Scholar 

  41. Mostashari F, Kulldorff M, Hartman JJ, Miller JR, Kulasekera V: Dead bird clusters as an early warning system for West Nile virus activity. Emerg Infect Dis. 2003, 9 (6): 641-646.

    Article  PubMed Central  PubMed  Google Scholar 

  42. Niklasson B, Hornfeldt B, Lundkvist A, Bjorsten S, Leduc J: Temporal dynamics of Puumala virus antibody prevalence in voles and of nephropathia epidemica incidence in humans. Am J Trop Med Hyg. 1995, 53 (2): 134-140.

    CAS  PubMed  Google Scholar 

  43. Niklasson B, Hornfeldt B, Lundman B: Could myocarditis, insulin-dependent diabetes mellitus, and Guillain-Barre syndrome be caused by one or more infectious agents carried by rodents?. Emerg Infect Dis. 1998, 4 (2): 187-193.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  44. Rab MA, Frame IA, Evans DA: The role of dogs in the epidemiology of human visceral leishmaniasis in northern Pakistan. Trans R Soc Trop Med Hyg. 1995, 89 (6): 612-615.

    Article  CAS  PubMed  Google Scholar 

  45. Shaman J, Day JF, Stieglitz M, Zebiak S, Cane M: Seasonal forecast of St. Louis encephalitis virus transmission, Florida. Emerg Infect Dis. 2004, 10 (5): 802-809.

    Article  PubMed Central  PubMed  Google Scholar 

  46. Theophilides CN, Ahearn SC, Grady S, Merlino M: Identifying West Nile virus risk areas: the Dynamic Continuous-Area Space-Time system. Am J Epidemiol. 2003, 157 (9): 843-854.

    Article  PubMed  Google Scholar 

  47. Wall PG, Morgan D, Lamden K, Griffin M, Threlfall EJ, Ward LR, Rowe B: Transmission of multi-resistant strains of Salmonella typhimurium from cattle to man. Vet Rec. 1995, 136 (23): 591-592.

    Article  CAS  PubMed  Google Scholar 

  48. Xu ZY, Tang YW, Kan LY, Tsai TF: Cats – source of protection or infection? A case-control study of hemorrhagic fever with renal syndrome. Am J Epidemiol. 1987, 126 (5): 942-948.

    CAS  PubMed  Google Scholar 

  49. Zeman P, Januska J: Epizootiologic background of dissimilar distribution of human cases of Lyme borreliosis and tick-borne encephalitis in a joint endemic area. Comp Immunol Microbiol Infect Dis. 1999, 22 (4): 247-260.

    Article  CAS  PubMed  Google Scholar 

  50. Zinsstag J, Roth F, Orkhon D, Chimed-Ochir G, Nansalmaa M, Kolar J, Vounatsou P: A model of animal-human brucellosis transmission in Mongolia. Prev Vet Med. 2005, 69 (1–2): 77-95.

    Article  CAS  PubMed  Google Scholar 

  51. Kulldorff M: A spatial scan statistic. Communications in Statistics – Theory and Methods. 1997, 26 (6): 1481-1496.

    Article  Google Scholar 

  52. Kulldorff M, Nagarwalla N: Spatial disease clusters: detection and inference. Stat Med. 1995, 14 (8): 799-810.

    Article  CAS  PubMed  Google Scholar 

  53. Bloom RM, Buckeridge DL, Cheng KE: Finding leading indicators for disease outbreaks: filtering, cross-correlation, and caveats. J Am Med Inform Assoc. 2007, 14 (1): 76-85.

    Article  PubMed Central  PubMed  Google Scholar 

  54. Hamori S: An Empirical Investigation of Stock Markets: The CCF Approach. Springer; 2003.

    Chapter  Google Scholar 

  55. Childs JE: Pre-spillover prevention of emerging zoonotic diseases: what are the targets and what are the tools?. Curr Top Microbiol Immunol. 2007, 315: 389-443.

    CAS  PubMed  Google Scholar 

  56. Turner AJ, Galvin JW, Rubira RJ, Miller GT: Anthrax explodes in an Australian summer. J Appl Microbiol. 1999, 87 (2): 196-199.

    Article  CAS  PubMed  Google Scholar 

  57. Aragao AI, Seoane AC, Leal TC, Leal NC, Almeida AM: [Surveillance of plague in the State of Ceara: 1990–1999]. Rev Soc Bras Med Trop. 2002, 35 (2): 143-148.

    Article  PubMed  Google Scholar 

  58. Marfin AA, Petersen LR, Eidson M, Miller J, Hadler J, Farello C, Werner B, Campbell GL, Layton M, Smith P, et al: Widespread West Nile virus activity, eastern United States, 2000. Emerg Infect Dis. 2001, 7 (4): 730-735.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  59. Levis S, Morzunov SP, Rowe JE, Enria D, Pini N, Calderon G, Sabattini M, St Jeor SC: Genetic diversity and epidemiology of hantaviruses in Argentina. J Infect Dis. 1998, 177 (3): 529-538.

    Article  CAS  PubMed  Google Scholar 

  60. Wagner MM, Moore AW, Aryel RM: Handbook of biosurveillance. Amsterdam; Boston: Academic Press; 2006.

    Google Scholar 

  61. One Health Initiative. [http://www.onehealthinitiative.com/]

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Acknowledgements

The authors would like to thank Daniel Chudnov for his programming work on the Canary Database and Martin Slade for his assistance with the statistical analysis of our study. This project is supported in part by The National Library of Medicine (NLM) grants TI5 LM007056 and K99 LM009825 to Matthew Scotch and G08 LM07881 to Peter Rabinowitz. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Library Of Medicine or the National Institutes of Health.

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MS conducted the literature review, developed the taxonomy, performed the analysis, and wrote the manuscript. LO conducted the literature review, developed the taxonomy, and reviewed the manuscript. PR developed the taxonomy and reviewed the manuscript. All authors read and approved the final manuscript.

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Scotch, M., Odofin, L. & Rabinowitz, P. Linkages between animal and human health sentinel data. BMC Vet Res 5, 15 (2009). https://doi.org/10.1186/1746-6148-5-15

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