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Changes in the Murine Microbiome and Bacterial Extracellular Vesicle Production in Response to Antibiotic Treatment and Norovirus Infection
Norovirus infection is influenced by the presence of commensal bacteria, and both human and murine norovirus (MNV) bind to these bacteria. These virus-bacterial interactions, as well as MNV infection, promote the increased production of bacterial extracellular vesicles (bEVs). However, no correlatio...
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Published in: | Viruses 2023-12, Vol.15 (12), p.2443 |
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description | Norovirus infection is influenced by the presence of commensal bacteria, and both human and murine norovirus (MNV) bind to these bacteria. These virus-bacterial interactions, as well as MNV infection, promote the increased production of bacterial extracellular vesicles (bEVs). However, no correlation has been made between specific bacterial groups, their vesicles, and their impact on norovirus infection. The current study evaluated the impact of select bacterial compositions of murine microbiomes using antibiotic (ABX) cocktails on MNV infection and bEV production. The goal of this research was to determine if increases in bEVs following MNV infection in mice were associated with changes in specific bacterial populations. Bacterial taxa were found to be differentially abundant in both ABX-treated and untreated mice, with the greatest change in bacterial taxa seen in mice treated with a broad-spectrum ABX cocktail. Specifically,
were found to be differentially abundant between a variety of treatment factors, including MNV infection. Overall, these results demonstrate that MNV infection can alter the abundance of bacterial taxa within the microbiota, as well as their production of extracellular vesicles, and that the use of selective antibiotic treatments can allow the detection of viral impacts on the microbiome that might otherwise be masked. |
doi_str_mv | 10.3390/v15122443 |
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were found to be differentially abundant between a variety of treatment factors, including MNV infection. Overall, these results demonstrate that MNV infection can alter the abundance of bacterial taxa within the microbiota, as well as their production of extracellular vesicles, and that the use of selective antibiotic treatments can allow the detection of viral impacts on the microbiome that might otherwise be masked.</description><identifier>ISSN: 1999-4915</identifier><identifier>EISSN: 1999-4915</identifier><identifier>DOI: 10.3390/v15122443</identifier><identifier>PMID: 38140684</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>16S sequencing ; Acids ; Animals ; Anti-Bacterial Agents - pharmacology ; Anti-Bacterial Agents - therapeutic use ; Antibiotics ; Bacteria ; bacterial extracellular vesicles ; Bacterial vesicles ; Bile ; Caliciviridae Infections ; Cell organelles ; Complications and side effects ; Development and progression ; Drinking water ; Extracellular vesicles ; Health aspects ; Host-bacteria relationships ; Humans ; Infections ; Lachnospiraeae ; Mice ; microbiome composition ; Microbiomes ; Microbiota ; Microbiota (Symbiotic organisms) ; murine norovirus ; Norovirus ; outer membrane vesicle ; Physiological aspects ; RNA virus infections ; Taxonomy ; Testing ; Viral infections</subject><ispartof>Viruses, 2023-12, Vol.15 (12), p.2443</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. 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 (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c441t-8a2dcae26376b052198e6b17b4252b617865ee1bae6ce05014f44ebb6dc7c0e43</cites><orcidid>0000-0002-5848-5229 ; 0000-0003-3159-246X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2904926954/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2904926954?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38140684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mosby, Chanel A</creatorcontrib><creatorcontrib>Long, Kendall J</creatorcontrib><creatorcontrib>Phillips, Matthew B</creatorcontrib><creatorcontrib>Bartel, Julia</creatorcontrib><creatorcontrib>Jones, Melissa K</creatorcontrib><title>Changes in the Murine Microbiome and Bacterial Extracellular Vesicle Production in Response to Antibiotic Treatment and Norovirus Infection</title><title>Viruses</title><addtitle>Viruses</addtitle><description>Norovirus infection is influenced by the presence of commensal bacteria, and both human and murine norovirus (MNV) bind to these bacteria. These virus-bacterial interactions, as well as MNV infection, promote the increased production of bacterial extracellular vesicles (bEVs). However, no correlation has been made between specific bacterial groups, their vesicles, and their impact on norovirus infection. The current study evaluated the impact of select bacterial compositions of murine microbiomes using antibiotic (ABX) cocktails on MNV infection and bEV production. The goal of this research was to determine if increases in bEVs following MNV infection in mice were associated with changes in specific bacterial populations. Bacterial taxa were found to be differentially abundant in both ABX-treated and untreated mice, with the greatest change in bacterial taxa seen in mice treated with a broad-spectrum ABX cocktail. Specifically,
were found to be differentially abundant between a variety of treatment factors, including MNV infection. 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were found to be differentially abundant between a variety of treatment factors, including MNV infection. Overall, these results demonstrate that MNV infection can alter the abundance of bacterial taxa within the microbiota, as well as their production of extracellular vesicles, and that the use of selective antibiotic treatments can allow the detection of viral impacts on the microbiome that might otherwise be masked.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38140684</pmid><doi>10.3390/v15122443</doi><orcidid>https://orcid.org/0000-0002-5848-5229</orcidid><orcidid>https://orcid.org/0000-0003-3159-246X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 16S sequencing Acids Animals Anti-Bacterial Agents - pharmacology Anti-Bacterial Agents - therapeutic use Antibiotics Bacteria bacterial extracellular vesicles Bacterial vesicles Bile Caliciviridae Infections Cell organelles Complications and side effects Development and progression Drinking water Extracellular vesicles Health aspects Host-bacteria relationships Humans Infections Lachnospiraeae Mice microbiome composition Microbiomes Microbiota Microbiota (Symbiotic organisms) murine norovirus Norovirus outer membrane vesicle Physiological aspects RNA virus infections Taxonomy Testing Viral infections |
title | Changes in the Murine Microbiome and Bacterial Extracellular Vesicle Production in Response to Antibiotic Treatment and Norovirus Infection |
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