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Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves

Diarrhea is a fatal disease to neonatal calves, and rotavirus is the main pathogen associated with neonatal calf diarrhea. Although previous studies have reported that the gut microbiota is changed in calves during diarrhea, less is known about whether rotavirus infection alters the structure of the...

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Autores principales: Jang, Ja-Young, Kim, Suhee, Kwon, Min-Sung, Lee, Jieun, Yu, Do-Hyeon, Song, Ru-Hui, Choi, Hak-Jong, Park, Jinho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Microbiological Society of Korea 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090552/
https://www.ncbi.nlm.nih.gov/pubmed/30456757
http://dx.doi.org/10.1007/s12275-019-8549-1
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author Jang, Ja-Young
Kim, Suhee
Kwon, Min-Sung
Lee, Jieun
Yu, Do-Hyeon
Song, Ru-Hui
Choi, Hak-Jong
Park, Jinho
author_facet Jang, Ja-Young
Kim, Suhee
Kwon, Min-Sung
Lee, Jieun
Yu, Do-Hyeon
Song, Ru-Hui
Choi, Hak-Jong
Park, Jinho
author_sort Jang, Ja-Young
collection PubMed
description Diarrhea is a fatal disease to neonatal calves, and rotavirus is the main pathogen associated with neonatal calf diarrhea. Although previous studies have reported that the gut microbiota is changed in calves during diarrhea, less is known about whether rotavirus infection alters the structure of the gut microbiota. Here, we characterized fecal microbial communities and identified possible relationships between the gut microbiota profiles and physiological parameters. Five fecal specimens of rotavirus-infected calves from 1 to 30 days after birth and five fecal specimens of age-matched healthy calves were used for the microbial community analysis using the Illumina MiSeq sequencer. Rotavirus infection was associated with reduced rotavirus infection significantly reduced the richness and diversity of the bacterial community. Weighted unique fraction metric analysis exhibited significant differences in community membership and structure between healthy and rotavirus-infected calves. Based on relative abundance analysis and linear discriminant analysis effect size, we found that the representative genera from Lactobacillus, Subdoligranulum, Blautia, and Bacteroides were closely related to healthy calves, while the genera Escherichia and Clostridium were closely affiliated to rotavirus-infected calves. Furthermore, canonical correlation analysis and Pearson correlation coefficient results revealed that the increased relative abundances of Lactobacillus, Subdoligranulum, and Bacteroides were correlated with normal levels of physiological characteristics such as white blood cells, blood urea nitrogen, serum amyloid protein A, and glucose concentration in serum. These results suggest that rotavirus infection alters the structure of the gut microbiota, correlating changes in physiological parameters. This study provides new information on the relationship between gut microbiota and the physiological parameters of rotavirus-mediated diarrheic calves.
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spelling pubmed-70905522020-03-24 Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves Jang, Ja-Young Kim, Suhee Kwon, Min-Sung Lee, Jieun Yu, Do-Hyeon Song, Ru-Hui Choi, Hak-Jong Park, Jinho J Microbiol Microbial Systematics and Evolutionary Microbiology Diarrhea is a fatal disease to neonatal calves, and rotavirus is the main pathogen associated with neonatal calf diarrhea. Although previous studies have reported that the gut microbiota is changed in calves during diarrhea, less is known about whether rotavirus infection alters the structure of the gut microbiota. Here, we characterized fecal microbial communities and identified possible relationships between the gut microbiota profiles and physiological parameters. Five fecal specimens of rotavirus-infected calves from 1 to 30 days after birth and five fecal specimens of age-matched healthy calves were used for the microbial community analysis using the Illumina MiSeq sequencer. Rotavirus infection was associated with reduced rotavirus infection significantly reduced the richness and diversity of the bacterial community. Weighted unique fraction metric analysis exhibited significant differences in community membership and structure between healthy and rotavirus-infected calves. Based on relative abundance analysis and linear discriminant analysis effect size, we found that the representative genera from Lactobacillus, Subdoligranulum, Blautia, and Bacteroides were closely related to healthy calves, while the genera Escherichia and Clostridium were closely affiliated to rotavirus-infected calves. Furthermore, canonical correlation analysis and Pearson correlation coefficient results revealed that the increased relative abundances of Lactobacillus, Subdoligranulum, and Bacteroides were correlated with normal levels of physiological characteristics such as white blood cells, blood urea nitrogen, serum amyloid protein A, and glucose concentration in serum. These results suggest that rotavirus infection alters the structure of the gut microbiota, correlating changes in physiological parameters. This study provides new information on the relationship between gut microbiota and the physiological parameters of rotavirus-mediated diarrheic calves. The Microbiological Society of Korea 2018-11-19 2019 /pmc/articles/PMC7090552/ /pubmed/30456757 http://dx.doi.org/10.1007/s12275-019-8549-1 Text en © The Microbiological Society of Korea and Springer Nature B.V. 2019 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Microbial Systematics and Evolutionary Microbiology
Jang, Ja-Young
Kim, Suhee
Kwon, Min-Sung
Lee, Jieun
Yu, Do-Hyeon
Song, Ru-Hui
Choi, Hak-Jong
Park, Jinho
Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title_full Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title_fullStr Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title_full_unstemmed Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title_short Rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
title_sort rotavirus-mediated alteration of gut microbiota and its correlation with physiological characteristics in neonatal calves
topic Microbial Systematics and Evolutionary Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090552/
https://www.ncbi.nlm.nih.gov/pubmed/30456757
http://dx.doi.org/10.1007/s12275-019-8549-1
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