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Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge

SIMPLE SUMMARY: Bovine respiratory disease is one of the greatest health challenges cattle producers face and is most commonly treated with antibiotics. With the current push to reduce the use of antibiotics in livestock production, producers are looking at non-pharmaceutical alternatives such as nu...

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Autores principales: Broadway, Paul Rand, Carroll, Jeffery, Burdick Sanchez, Nicole, Word, Alyssa, Roberts, Shelby, Kaufman, Emily, Richeson, John, Brown, Mike, Ridenour, Ken
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000065/
https://www.ncbi.nlm.nih.gov/pubmed/33804483
http://dx.doi.org/10.3390/ani11030646
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author Broadway, Paul Rand
Carroll, Jeffery
Burdick Sanchez, Nicole
Word, Alyssa
Roberts, Shelby
Kaufman, Emily
Richeson, John
Brown, Mike
Ridenour, Ken
author_facet Broadway, Paul Rand
Carroll, Jeffery
Burdick Sanchez, Nicole
Word, Alyssa
Roberts, Shelby
Kaufman, Emily
Richeson, John
Brown, Mike
Ridenour, Ken
author_sort Broadway, Paul Rand
collection PubMed
description SIMPLE SUMMARY: Bovine respiratory disease is one of the greatest health challenges cattle producers face and is most commonly treated with antibiotics. With the current push to reduce the use of antibiotics in livestock production, producers are looking at non-pharmaceutical alternatives such as nutritional supplements. This study aimed to determine if different forms of zinc supplementation could reduce some of the negative health effects associated with bovine respiratory disease. Overall, cattle supplemented with ZinMet (zinc methionine/organic zinc) responded better during the disease as evidenced by blood parameters, decreased lesion severity, and decreased fever. Conversely, cattle fed a large dose of zinc sulfate (inorganic zinc) displayed a higher fever and blood parameters that indicated a greater sickness response. Findings from this study suggest that the type and amount of zinc fed to cattle may influence their response to bovine respiratory disease. ABSTRACT: To determine the effects of zinc supplementation on the immune response to a combined viral-bacterial respiratory disease challenge, thirty-two beef heifers (255 ± 15 kg) were subjected to a 30-d period of Zn depletion, then randomly assigned to one of three treatment diets fed for 30 d before the challenge: (1) supplementation with 100 mg of Zn from Zn sulfate/kg of DM (Zn100), (2) supplementation with 200 mg of Zn from Zn sulfate/kg of DM (Zn200), and (3) supplementation with 80 mg of Zn/kg of DM from zinc methionine and 20 mg of Zn from Zn sulfate/kg of DM (ZinMet). After the 30-d supplementation period, all heifers were fitted with indwelling vaginal temperature (VT) devices and intra-nasally challenged with 1 × 10(8) PFU bovine herpesvirus-1 on d -3, and then allowed to rest in outdoor pens for 3 d. On d 0, each heifer was challenged intra-tracheally with an average dose of 2.38 × 10(7) CFU Mannheimia haemolytica (MH), fitted with an indwelling jugular catheter, and then moved into individual stalls in an environmentally-controlled enclosed barn. Whole blood samples were collected at 1-h (serum) and 2-h (complete blood counts) intervals from 0 to 8 h, and at 12, 24, 36, 48, 60, 72, 168, and 360 h relative to MH challenge. Data were analyzed using the MIXED procedure of SAS specific for repeated measures with fixed effects of treatment, time, and their interaction. There was a treatment effect (p < 0.01) for VT such that Zn200 heifers had greater VT than Zn100 and ZinMet heifers. There was a trend (p = 0.10) for a serum cortisol treatment effect with Zn100 heifers having greater cortisol than ZinMet heifers. Total leukocytes and lymphocytes were greater (p ≤ 0.01) in Zn100 heifers than Zn200 and ZinMet heifers, whereas monocytes were less (p = 0.05) in ZinMet heifers than Zn100 and Zn200 heifers. Concentrations of IL-6 were greater (p = 0.02) in ZinMet heifers than Zn100 and Zn200 heifers. Concentrations of IFN-γ were greater in Zn200 heifers than ZinMet heifers at 0 h, and Zn100 heifers from 0 to 12 h post-MH challenge (treatment x time p = 0.02). Serum haptoglobin was not affected by treatment or treatment x time (p ≥ 0.36) but increased over time (p < 0.01) in all groups. There was a trend (p = 0.11) for ZinMet heifers to have less severe nasal lesion scores than Zn100 heifers. The observed differential physiological responses in this study indicate that zinc source and concentration may alter the response to a bovine respiratory challenge in heifers.
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spelling pubmed-80000652021-03-28 Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge Broadway, Paul Rand Carroll, Jeffery Burdick Sanchez, Nicole Word, Alyssa Roberts, Shelby Kaufman, Emily Richeson, John Brown, Mike Ridenour, Ken Animals (Basel) Article SIMPLE SUMMARY: Bovine respiratory disease is one of the greatest health challenges cattle producers face and is most commonly treated with antibiotics. With the current push to reduce the use of antibiotics in livestock production, producers are looking at non-pharmaceutical alternatives such as nutritional supplements. This study aimed to determine if different forms of zinc supplementation could reduce some of the negative health effects associated with bovine respiratory disease. Overall, cattle supplemented with ZinMet (zinc methionine/organic zinc) responded better during the disease as evidenced by blood parameters, decreased lesion severity, and decreased fever. Conversely, cattle fed a large dose of zinc sulfate (inorganic zinc) displayed a higher fever and blood parameters that indicated a greater sickness response. Findings from this study suggest that the type and amount of zinc fed to cattle may influence their response to bovine respiratory disease. ABSTRACT: To determine the effects of zinc supplementation on the immune response to a combined viral-bacterial respiratory disease challenge, thirty-two beef heifers (255 ± 15 kg) were subjected to a 30-d period of Zn depletion, then randomly assigned to one of three treatment diets fed for 30 d before the challenge: (1) supplementation with 100 mg of Zn from Zn sulfate/kg of DM (Zn100), (2) supplementation with 200 mg of Zn from Zn sulfate/kg of DM (Zn200), and (3) supplementation with 80 mg of Zn/kg of DM from zinc methionine and 20 mg of Zn from Zn sulfate/kg of DM (ZinMet). After the 30-d supplementation period, all heifers were fitted with indwelling vaginal temperature (VT) devices and intra-nasally challenged with 1 × 10(8) PFU bovine herpesvirus-1 on d -3, and then allowed to rest in outdoor pens for 3 d. On d 0, each heifer was challenged intra-tracheally with an average dose of 2.38 × 10(7) CFU Mannheimia haemolytica (MH), fitted with an indwelling jugular catheter, and then moved into individual stalls in an environmentally-controlled enclosed barn. Whole blood samples were collected at 1-h (serum) and 2-h (complete blood counts) intervals from 0 to 8 h, and at 12, 24, 36, 48, 60, 72, 168, and 360 h relative to MH challenge. Data were analyzed using the MIXED procedure of SAS specific for repeated measures with fixed effects of treatment, time, and their interaction. There was a treatment effect (p < 0.01) for VT such that Zn200 heifers had greater VT than Zn100 and ZinMet heifers. There was a trend (p = 0.10) for a serum cortisol treatment effect with Zn100 heifers having greater cortisol than ZinMet heifers. Total leukocytes and lymphocytes were greater (p ≤ 0.01) in Zn100 heifers than Zn200 and ZinMet heifers, whereas monocytes were less (p = 0.05) in ZinMet heifers than Zn100 and Zn200 heifers. Concentrations of IL-6 were greater (p = 0.02) in ZinMet heifers than Zn100 and Zn200 heifers. Concentrations of IFN-γ were greater in Zn200 heifers than ZinMet heifers at 0 h, and Zn100 heifers from 0 to 12 h post-MH challenge (treatment x time p = 0.02). Serum haptoglobin was not affected by treatment or treatment x time (p ≥ 0.36) but increased over time (p < 0.01) in all groups. There was a trend (p = 0.11) for ZinMet heifers to have less severe nasal lesion scores than Zn100 heifers. The observed differential physiological responses in this study indicate that zinc source and concentration may alter the response to a bovine respiratory challenge in heifers. MDPI 2021-03-01 /pmc/articles/PMC8000065/ /pubmed/33804483 http://dx.doi.org/10.3390/ani11030646 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Broadway, Paul Rand
Carroll, Jeffery
Burdick Sanchez, Nicole
Word, Alyssa
Roberts, Shelby
Kaufman, Emily
Richeson, John
Brown, Mike
Ridenour, Ken
Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title_full Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title_fullStr Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title_full_unstemmed Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title_short Zinc Source and Concentration Altered Physiological Responses of Beef Heifers during a Combined Viral-Bacterial Respiratory Challenge
title_sort zinc source and concentration altered physiological responses of beef heifers during a combined viral-bacterial respiratory challenge
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000065/
https://www.ncbi.nlm.nih.gov/pubmed/33804483
http://dx.doi.org/10.3390/ani11030646
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