Environmental remodeling of human gut microbiota and antibiotic resistome in livestock farms

Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposur...

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Published inNature communications Vol. 11; no. 1; pp. 1427 - 11
Main Authors Sun, Jian, Liao, Xiao-Ping, D’Souza, Alaric W., Boolchandani, Manish, Li, Sheng-Hui, Cheng, Ke, Luis Martínez, José, Li, Liang, Feng, You-Jun, Fang, Liang-Xing, Huang, Ting, Xia, Jing, Yu, Yang, Zhou, Yu-Feng, Sun, Yong-Xue, Deng, Xian-Bo, Zeng, Zhen-Ling, Jiang, Hong-Xia, Fang, Bing-Hu, Tang, You-Zhi, Lian, Xin-Lei, Zhang, Rong-Min, Fang, Zhi-Wei, Yan, Qiu-Long, Dantas, Gautam, Liu, Ya-Hong
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 18.03.2020
Nature Publishing Group
Nature Portfolio
Subjects
Online AccessGet full text
ISSN2041-1723
2041-1723
DOI10.1038/s41467-020-15222-y

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Abstract Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students’ gut microbiomes and resistomes to farm workers’ and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human’s living environment can persistently shape their gut microbiota and antibiotic resistome. Environments where antibiotics are used indiscriminately exhibit microbial communities that can represent hot-spots of resistance gene enrichment, which in turn could spread to humans. Here, the authors characterize how exposure to swine farms environment lead to temporal changes in the gut microbiome and resistome of healthy veterinary students.
AbstractList Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students’ gut microbiomes and resistomes to farm workers’ and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human’s living environment can persistently shape their gut microbiota and antibiotic resistome.Environments where antibiotics are used indiscriminately exhibit microbial communities that can represent hot-spots of resistance gene enrichment, which in turn could spread to humans. Here, the authors characterize how exposure to swine farms environment lead to temporal changes in the gut microbiome and resistome of healthy veterinary students.
Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students’ gut microbiomes and resistomes to farm workers’ and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human’s living environment can persistently shape their gut microbiota and antibiotic resistome.
Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students’ gut microbiomes and resistomes to farm workers’ and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human’s living environment can persistently shape their gut microbiota and antibiotic resistome. Environments where antibiotics are used indiscriminately exhibit microbial communities that can represent hot-spots of resistance gene enrichment, which in turn could spread to humans. Here, the authors characterize how exposure to swine farms environment lead to temporal changes in the gut microbiome and resistome of healthy veterinary students.
Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students' gut microbiomes and resistomes to farm workers' and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human's living environment can persistently shape their gut microbiota and antibiotic resistome.Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined and controlled swine farm environments on temporal changes in the gut microbiome and resistome of veterinary students with occupational exposure for 3 months. By analyzing 16S rRNA and whole metagenome shotgun sequencing data in tandem with culture-based methods, we show that farm exposure shapes the gut microbiome of students, resulting in enrichment of potentially pathogenic taxa and antimicrobial resistance genes. Comparison of students' gut microbiomes and resistomes to farm workers' and environmental samples revealed extensive sharing of resistance genes and bacteria following exposure and after three months of their visit. Notably, antibiotic resistance genes were found in similar genetic contexts in student samples and farm environmental samples. Dynamic Bayesian network modeling predicted that the observed changes partially reverse over a 4-6 month period. Our results indicate that acute changes in a human's living environment can persistently shape their gut microbiota and antibiotic resistome.
Environments where antibiotics are used indiscriminately exhibit microbial communities that can represent hot-spots of resistance gene enrichment, which in turn could spread to humans. Here, the authors characterize how exposure to swine farms environment lead to temporal changes in the gut microbiome and resistome of healthy veterinary students.
ArticleNumber 1427
Author Luis Martínez, José
Liu, Ya-Hong
Dantas, Gautam
Cheng, Ke
Zhou, Yu-Feng
Fang, Bing-Hu
Tang, You-Zhi
Li, Sheng-Hui
Yu, Yang
Li, Liang
Feng, You-Jun
Sun, Yong-Xue
Fang, Zhi-Wei
Xia, Jing
Yan, Qiu-Long
Zhang, Rong-Min
Fang, Liang-Xing
Liao, Xiao-Ping
Zeng, Zhen-Ling
Sun, Jian
Boolchandani, Manish
Lian, Xin-Lei
Deng, Xian-Bo
D’Souza, Alaric W.
Huang, Ting
Jiang, Hong-Xia
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– sequence: 6
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– sequence: 8
  givenname: Liang
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  organization: National Risk Assessment Laboratory for Antimicrobial Resistance of Animal Original Bacteria, South China Agricultural University, Guangdong Laboratory for Lingnan Modern Agriculture
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  givenname: You-Jun
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  givenname: Liang-Xing
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  surname: Jiang
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/32188862$$D View this record in MEDLINE/PubMed
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– volume: 25
  start-page: 1966
  year: 2009
  ident: 15222_CR47
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btp336
– volume: 15
  year: 2014
  ident: 15222_CR8
  publication-title: Genome Biol.
  doi: 10.1186/gb-2014-15-7-r89
SSID ssj0000391844
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Snippet Anthropogenic environments have been implicated in enrichment and exchange of antibiotic resistance genes and bacteria. Here we study the impact of confined...
Environments where antibiotics are used indiscriminately exhibit microbial communities that can represent hot-spots of resistance gene enrichment, which in...
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SubjectTerms 45/23
45/77
631/114/2412
631/326/22/1434
631/326/2565/2134
631/326/2565/855
631/326/41/2142
Adult
Animals
Anthropogenic factors
Anti-Bacterial Agents - pharmacology
Antibiotic resistance
Antibiotics
Antimicrobial resistance
Bacteria
Bacteria - classification
Bacteria - drug effects
Bacteria - genetics
Bacteria - isolation & purification
Bayesian analysis
Drug resistance
Drug Resistance, Bacterial
Enrichment
Exposure
Farms
Farmworkers
Gastrointestinal Microbiome
Gastrointestinal Tract - microbiology
Genes
Gut microbiota
Human influences
Humanities and Social Sciences
Humans
Intestinal microflora
Livestock
Livestock farming
Male
Microbial activity
Microbiomes
Microbiota
Microorganisms
multidisciplinary
Occupational Exposure
Occupational health
rRNA 16S
Schools, Veterinary
Science
Science (multidisciplinary)
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Swine
Swine - microbiology
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Title Environmental remodeling of human gut microbiota and antibiotic resistome in livestock farms
URI https://link.springer.com/article/10.1038/s41467-020-15222-y
https://www.ncbi.nlm.nih.gov/pubmed/32188862
https://www.proquest.com/docview/2378839427
https://www.proquest.com/docview/2379028901
https://pubmed.ncbi.nlm.nih.gov/PMC7080799
https://doaj.org/article/f43a980b278f48d79417afb240dde2c7
Volume 11
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