Cargando…

Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics

Improper use of antibiotics in swine could reduce commensal bacteria and possibly increase pathogen infections via the gut resistome. This study aimed to compare the metaproteomic profiles of the gut resistome and related metabolism in the cecal microbiota of fattening pigs raised under antibiotic-f...

Descripción completa

Detalles Bibliográficos
Autores principales: Buthasane, Pamornya, Roytrakul, Sittiruk, Phaonakrop, Narumon, Tunsagool, Paiboon, Buthasane, Wannapol, Am-in, Nutthee, Suriyaphol, Gunnaporn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433946/
https://www.ncbi.nlm.nih.gov/pubmed/37439677
http://dx.doi.org/10.1128/spectrum.02223-23
_version_ 1785091765924003840
author Buthasane, Pamornya
Roytrakul, Sittiruk
Phaonakrop, Narumon
Tunsagool, Paiboon
Buthasane, Wannapol
Am-in, Nutthee
Suriyaphol, Gunnaporn
author_facet Buthasane, Pamornya
Roytrakul, Sittiruk
Phaonakrop, Narumon
Tunsagool, Paiboon
Buthasane, Wannapol
Am-in, Nutthee
Suriyaphol, Gunnaporn
author_sort Buthasane, Pamornya
collection PubMed
description Improper use of antibiotics in swine could reduce commensal bacteria and possibly increase pathogen infections via the gut resistome. This study aimed to compare the metaproteomic profiles of the gut resistome and related metabolism in the cecal microbiota of fattening pigs raised under antibiotic-free (ABF) conditions with those of ordinary industrial pigs (controls [CTRL]). The top three relatively abundant microbes in both groups were Escherichia coli, Ruminococcus, and Lactobacillus, followed by Bacteroides and Bifidobacterium. E. coli, Lactobacillus, and Bacteroides were found to be increased in the CTRL group, whereas Ruminococcus and Clostridium were greater in the ABF group. The highest abundances of antibiotic resistance proteins (log(2) expression levels [ELs] of >10) were found to be for tetracycline resistance (Tet(r)) and aminoglycoside resistance (AMG(r)) proteins found in Bacteroides, with a significant increase in the CTRL group. High Tet(r) (ELs of 5.32) was found in Ruminococcus in the CTRL group, although pigs in both groups had never received tetracycline, possibly reflecting the influence of environments in farms. In E. coli, AMG(r) and β-lactamase family proteins were observed in both groups (ELs of 3 to 6), whereas multidrug resistance protein MdtL was significantly expressed in the CTRL group (ELs of around 3). In the ABF group, CRISPR-associated endonucleases Cas1 and Cas9, which function to defend against viruses, were markedly observed in Ruminococcus and Lactobacillus, respectively, with ELs of 8.6 and 4.15, respectively. In conclusion, this study demonstrated that CRISPR-associated endonucleases were markedly observed in the ABF group, whereas higher levels of Tet(r), AMG(r), and multidrug resistance protein MdtL was markedly observed in dominant bacterial species in the CTRL group. IMPORTANCE In order to control and reduce antibiotic use in animals, the Department of Livestock Development, Thailand, has launched a campaign for antibiotic-free livestock production. The present study has shown for the first time that CRISPR-associated endonucleases Cas1 and Cas9, which function to defend against viruses, were markedly observed in Ruminococcus and Lactobacillus, respectively, in ceca of pigs raised without antibiotics (ABF). The highest abundances of antibiotic resistance proteins were for tetracycline (Tet(r)) and aminoglycoside resistance (AMG(r)) proteins found in Bacteroides, with a significant increase in the controls. In E. coli, the microbe with the highest relative abundance, AMG(r) and β-lactamase family proteins were observed in both groups, whereas multidrug resistance protein MdtL was significantly expressed in the controls. Pigs in both ABF and control groups had never received tetracycline, possibly reflecting the influence of farm environments. We suggest that pigs raised without antibiotics may have more beneficial microorganisms for the gut than pigs raised with antibiotics.
format Online
Article
Text
id pubmed-10433946
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-104339462023-08-18 Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics Buthasane, Pamornya Roytrakul, Sittiruk Phaonakrop, Narumon Tunsagool, Paiboon Buthasane, Wannapol Am-in, Nutthee Suriyaphol, Gunnaporn Microbiol Spectr Research Article Improper use of antibiotics in swine could reduce commensal bacteria and possibly increase pathogen infections via the gut resistome. This study aimed to compare the metaproteomic profiles of the gut resistome and related metabolism in the cecal microbiota of fattening pigs raised under antibiotic-free (ABF) conditions with those of ordinary industrial pigs (controls [CTRL]). The top three relatively abundant microbes in both groups were Escherichia coli, Ruminococcus, and Lactobacillus, followed by Bacteroides and Bifidobacterium. E. coli, Lactobacillus, and Bacteroides were found to be increased in the CTRL group, whereas Ruminococcus and Clostridium were greater in the ABF group. The highest abundances of antibiotic resistance proteins (log(2) expression levels [ELs] of >10) were found to be for tetracycline resistance (Tet(r)) and aminoglycoside resistance (AMG(r)) proteins found in Bacteroides, with a significant increase in the CTRL group. High Tet(r) (ELs of 5.32) was found in Ruminococcus in the CTRL group, although pigs in both groups had never received tetracycline, possibly reflecting the influence of environments in farms. In E. coli, AMG(r) and β-lactamase family proteins were observed in both groups (ELs of 3 to 6), whereas multidrug resistance protein MdtL was significantly expressed in the CTRL group (ELs of around 3). In the ABF group, CRISPR-associated endonucleases Cas1 and Cas9, which function to defend against viruses, were markedly observed in Ruminococcus and Lactobacillus, respectively, with ELs of 8.6 and 4.15, respectively. In conclusion, this study demonstrated that CRISPR-associated endonucleases were markedly observed in the ABF group, whereas higher levels of Tet(r), AMG(r), and multidrug resistance protein MdtL was markedly observed in dominant bacterial species in the CTRL group. IMPORTANCE In order to control and reduce antibiotic use in animals, the Department of Livestock Development, Thailand, has launched a campaign for antibiotic-free livestock production. The present study has shown for the first time that CRISPR-associated endonucleases Cas1 and Cas9, which function to defend against viruses, were markedly observed in Ruminococcus and Lactobacillus, respectively, in ceca of pigs raised without antibiotics (ABF). The highest abundances of antibiotic resistance proteins were for tetracycline (Tet(r)) and aminoglycoside resistance (AMG(r)) proteins found in Bacteroides, with a significant increase in the controls. In E. coli, the microbe with the highest relative abundance, AMG(r) and β-lactamase family proteins were observed in both groups, whereas multidrug resistance protein MdtL was significantly expressed in the controls. Pigs in both ABF and control groups had never received tetracycline, possibly reflecting the influence of farm environments. We suggest that pigs raised without antibiotics may have more beneficial microorganisms for the gut than pigs raised with antibiotics. American Society for Microbiology 2023-07-13 /pmc/articles/PMC10433946/ /pubmed/37439677 http://dx.doi.org/10.1128/spectrum.02223-23 Text en Copyright © 2023 Buthasane et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Buthasane, Pamornya
Roytrakul, Sittiruk
Phaonakrop, Narumon
Tunsagool, Paiboon
Buthasane, Wannapol
Am-in, Nutthee
Suriyaphol, Gunnaporn
Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title_full Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title_fullStr Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title_full_unstemmed Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title_short Metaproteomic Analysis of Gut Resistome in the Cecal Microbiota of Fattening Pigs Raised without Antibiotics
title_sort metaproteomic analysis of gut resistome in the cecal microbiota of fattening pigs raised without antibiotics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433946/
https://www.ncbi.nlm.nih.gov/pubmed/37439677
http://dx.doi.org/10.1128/spectrum.02223-23
work_keys_str_mv AT buthasanepamornya metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT roytrakulsittiruk metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT phaonakropnarumon metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT tunsagoolpaiboon metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT buthasanewannapol metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT aminnutthee metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics
AT suriyapholgunnaporn metaproteomicanalysisofgutresistomeinthececalmicrobiotaoffatteningpigsraisedwithoutantibiotics