Elsevier

Livestock Science

Volume 232, February 2020, 103918
Livestock Science

Post-weaning rumen fermentation of Simmental calves in response to weaning age and relationship with rumination time measured by the Hr-Tag rumination-monitoring system

https://doi.org/10.1016/j.livsci.2020.103918Get rights and content

Highligths

  • Response of weaning at an early age on rumen pH, rumen fermentation, dietary intake, growth rate in the post-weaning phase, and rumination behavior employing the Hr-Tag rumination-monitoring system (Hr-Tag; SCR Engineers Ltd, Netanya, Israel) in Simmental calves.

  • Weaning Simmental calves at 45 d of age compared with 60 d, fed whole milk in the pre-weaning period, did not impair rumen fermentation after weaning, and overall the rate of VFAs clearance have a major impact on ruminal pH.

  • Daily rumination time measured by Hr-Tags positively correlated to pH and negatively correlated to concentration of total VFAs, acetate, and propionate. A positive linear relationship was also found between daily rumination time and the molar proportion of acetate:propionate ratio.

  • The use of Hr-Tags could give quick information on rumen health and thus to identify in a timely fashion those calves at a greater risk (i.e. marked decrease of rumen pH) during this critical phase, from liquid to only solid feeds.

Abstract

The present experiment aimed to investigate (1) the effect of weaning age on rumen fermentation, dietary intake, growth, and rumination behavior at 20 d after weaning in Simmental calves, and (2) the relationship between rumination time measured by the Hr-Tag rumination-monitoring system (Hr-Tag; SCR Engineers Ltd, Netanya, Israel) and rumen fermentation variables. Ten Simmental calves were randomly assigned at birth to be weaned at 45 (early weaning, EW) or 60 d of age (normal weaning, NW). EW calves were offered 6 L of bulk whole milk/d from d 2 to 38 and 3 L/d from d 39 to 45, while NW were offered 6 L of bulk whole milk/d from d 2 to 53 and 3 L/d from d 54 to 60. Individual calf starter intake was recorded daily and average daily gain (ADG) was calculated taken into account the BW at 6 d after weaning and final BW at 20 d after weaning. On d 20 after weaning, samples of rumen fluid were obtained via an esophageal tube. These samples were used to determine pH and volatile fatty acids (VFAs) concentration. Throughout the entire experiment, the Hr-Tag system continuously recorded the rumination time (RT) by Hr-Tag loggers positioned on the left side of the neck. No treatment differences were detected for total VFAs concentration and molar proportion of acetate, propionate, and butyrate (P > 0.05). Overall in the period -25 to 20 d relative to weaning time, daily RT did not differ between NW and EW calves and it increased around weaning in both groups. Hr-Tags revealed no differences in daily RT pattern (2h-RT) during the 3 d before rumen collection, while during the day (24 h) 2h-RT significantly varied overall in both EW and NW groups. Daily RT measured by Hr-Tags positively correlated to pH (r = 0.98; P < 0.001), and negatively correlated to concentration of total VFAs (r = −0.90; P < 0.001), acetate (r = −0.85; P < 0.001), and propionate (r = −0.90; P < 0.001). On the contrary, a positive linear relationship was found between daily RT and the molar proportion of acetate:propionate ratio (R2 = 0.76; P = 0.002). Results herein provide evidence that early weaning (45 d) in Simmental calves fed whole milk in the pre-weaning period did not impair rumen fermentations 20 d after weaning and BW gain. Surprisingly, the use of Hr-Tags could prove interesting for the prediction of rumen fermentation characteristics and patterns in calves after weaning. The collected data could be used to obtain quick information on rumen functionality allowing the identification in a timely fashion of those calves at a greater risk (i.e. marked decrease of rumen pH) during this critical transition phase, from liquid to only solid feeds, when rumen of calves is not completely developed and efficient. The provision of these results from Hr-Tags in calves may give some input for further research involving a greater number of calves to better establish correlations with phenotypic variables. Moreover, this device could be adopted in studies focused on the effect of different pre- and post-weaning diets or weaning management.

Introduction

The dairy industry has always been witness to the ongoing debate between dairy farmers and researcher regarding the optimal earliest weaning age for dairy calves in order to limit labor, management time, and feed costs. Weaning calves as early as 3 to 7 weeks results in time and monetary savings by reducing labor without negative effects on growth through 8 weeks of age (Kehoe et al., 2007; Winter, 1985). Starting from the second week of age, calves are able to produce some fermentation end products in the rumen (Beharka et al., 1998) and at 8 weeks of age (with concentrate diets) VFA concentrations reach approximately ranges normally observed in adult ruminants (Suárez et al., 2006). Rumen fermentation starts at a very young age and VFA concentrations increase with increasing solid feed intake. Thus, after calves start consuming solid feed, the level and physical-chemical nature of available substrate affects rumen microbial diversity and subsequent fermentation patterns (Lesmeister and Heinrichs, 2004). It has been reported previously that concentrate diets generally favor starch digesters in the rumen and tend to result in increased butyrate and propionate molar proportions at the expense of acetate (Schwartzkopf-Genswein et al., 2003). However, when forages are provided, cellulolytic microbial growth is enhanced with consequent increased molar proportions of acetate in the rumen (Žitnan et al., 1998). In addition, Calsamiglia et al. (2008) indicated that a combination of both pH (between 4.9 and 7) and type of substrate (400 or 900 g concentrate/Kg) were responsible for the fermentation pattern and concentration of particular VFA in the rumen. Therefore, ruminal pH is also crucial for normal rumen development, rumen fermentation, and overall calf health. Hence, development of the rumen coincides with increased absorption of VFA, the main end products from solid feed fermentation and the primary energy source of weaned ruminants (Baldwin et al., 2004).

Since rumen development has a clear and major impact on the digestive capabilities and supply of substrates to the growing ruminant, there is still a necessity to address studies and efforts on how to reliably measure rumen development. Indeed, it has been indicated that rumination accompanies or precedes the development of normal rumen function and fermentation (Swanson and Harris, 1958). In this respect, the recent introduction of indirect methods to measure rumination time (RT), based on analysis of vocal signs (Hi-Tag rumination monitoring system, SCR Engineers Ltd., Netanya, Israel), allows automatic measurement of RT and analysis of daily pattern in RT. In our previous study (Lopreiato et al., 2018), the application of the Hr-Tag rumination monitoring system highlighted the daily pattern of rumination in pre-weaned calves, showing a distinct daily behavior, as observable in adult cattle. More recently, Rodrigues et al. (2019) reported the ability of this device to detect changes in the rumination pattern of calves throughout the weaning period (pre-weaning, at weaning and post-weaning).

Our study aimed to evaluate the response of weaning at an early age on rumen pH, rumen fermentation, dietary intake, growth rate in the post-weaning phase, and rumination behavior employing the Hr-Tag rumination-monitoring system (Hr-Tag; SCR Engineers Ltd, Netanya, Israel) in Simmental calves. In addition, a secondary objective was to evaluate the relationship between data obtained by Hr-Tags and rumen fermentation variables.

Section snippets

Calves management, experimental design, and rumination measures

All performed procedures followed the common good clinical practices (EMA, 2000. VICH GL9: Guideline on Good Clinical Practice EMA/CVMP/VICH/463202/2009) and received an institutional approval by Ethical Animal Care and Use Committee of the Magna Graecia University of Catanzaro (Protocol No. 271/2017). Moreover, the farmer was previously informed and assured its compliance with purposes and methods of the research.

Ten Simmental calves were enrolled in the study within 1 h from birth, after

Growth, intake and RT by Hr-tag system

The final BW was affected by weaning period (Wp: P < 0.05; Fig. 1), resulting in NW calves with greater BW (± SD) compared with EW (129 ± 3.59 vs 114 ± 4.62 Kg, respectively). However, no differences were obtained for ADG (1.20 ± 0.16 and 1.33 ± 0.21 kg/d, respectively for EW and NW calves) between groups, calculated from 6 days after weaning (P > 0.05).

The interaction Wp x Day (P < 0.01) showed that differences in starter intake between groups were achieved after weaning (Fig. 2a), where

Discussion

The present experiment aimed to enroll Simmental calves (cattle breed selected for meat and milk production) in order to evaluate the effect of an early weaning (45 d) compared with a normal weaning (60 d) age on starter intake, post-weaning growth, behavior (ruminating), and rumen fermentation efficiency. In addition, we have been able to highlight a relationship between rumen fermentation characteristics and RT continuously recorded by using the Hr-Tag rumination-monitoring system (Lopreiato

Conclusion

With the present experiment we provided evidence for the use of Hr-Tags in the prediction of rumen fermentation characteristics in calves after weaning, making it a useful approach for obtaining quick information on rumen functionality. Finally, weaning Simmental calves at 45 d of age, fed whole milk in the pre-weaning period, did not impair rumen fermentations measured 20 d after weaning, suggesting that an early weaning date to reduce rearing cost might not jeopardize calf development.

Declaration of Competing Interest

The authors declare no conflicts of interest.

Acknowledgments

This project was financially supported by the Interdepartment Services Centre of Veterinary for Human and Animal Health (Magna Graecia University, Catanzaro, Italy), by the Department of Animal Science, Food and Nutrition (DiANA; Università Cattolica del Sacro Cuore, Piacenza, Italy), and by the “Romeo ed Enrica Invernizzi Foundation” (Milan, Italy). The authors thank Tsur Hadar and Dr. Rachel Toaff (SCR Engineers Ltd., Netanya, Israel) for their technical support, and Fattoria Demetra for

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