Loading…

Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies

Background Short‐term antibiotics exposure is associated with alterations in microbiota and antibiotic resistance genes (ARGs) in the human gut. While antibiotics are critical in the successful eradication of Helicobacter pylori, the short‐term and long‐term impacts on the composition and quantity o...

Full description

Saved in:
Bibliographic Details
Published in:Helicobacter (Cambridge, Mass.) Mass.), 2022-04, Vol.27 (2), p.e12871-n/a
Main Authors: Wang, Lingling, Yao, Haobin, Tong, Teresa, Lau, KamShing, Leung, Suet Yi, Ho, Joshua W. K., Leung, Wai K.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533
cites cdi_FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533
container_end_page n/a
container_issue 2
container_start_page e12871
container_title Helicobacter (Cambridge, Mass.)
container_volume 27
creator Wang, Lingling
Yao, Haobin
Tong, Teresa
Lau, KamShing
Leung, Suet Yi
Ho, Joshua W. K.
Leung, Wai K.
description Background Short‐term antibiotics exposure is associated with alterations in microbiota and antibiotic resistance genes (ARGs) in the human gut. While antibiotics are critical in the successful eradication of Helicobacter pylori, the short‐term and long‐term impacts on the composition and quantity of antibiotics resistance genes after H. pylori eradication are unclear. This study used whole‐genome shotgun metagenomic of stool samples to characterize the gut microbiota and ARGs, before and after H. pylori eradication therapy. Results Forty‐four H. pylori‐infected patients were recruited, including 21 treatment naïve patients who received clarithromycin‐based triple therapy (CLA group) and 23 patients who failed previous therapies, in which 10 received levofloxacin‐based quadruple therapy (LEVO group) and 13 received other combinations (OTHER group). Stool samples were collected at baseline (before current treatment), 6 week and 6 month after eradication therapy. At baseline, there was only a slight difference among the three groups on ARGs and gut microbiota. After eradication therapy, there was a transient but significant increase in gut ARGs 6 week post‐therapy, among which the LEVO group had the most significant ARGs alteration compared to other two groups. For treatment naïve patients, those with higher ErmF abundance were prone to fail CLA eradication and gain more ARGs after treatment. For gut microbiota, the bacteria richness decreased at 6 week and there was a significant difference in microbiota community among the three groups at 6 week. Conclusions Our findings demonstrated the dynamic alterations in gut microbiota and ARGs induced by different eradication therapies, which could influence the choices of antibiotics in eradication therapy.
doi_str_mv 10.1111/hel.12871
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2615920027</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2615920027</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533</originalsourceid><addsrcrecordid>eNp1kUFvFCEUx4mxsbV68AsYEi96mJYHwzBzNLW6TTbppZ4nD-axSzPLbGEmzX57Wbd6MJED8ODHL8CfsQ8grqC06y2NVyBbA6_YBWipKq1M-7rMRauqWrXdOXub86MQQqu6e8POS9900MAFe_p2iLgLjrstxg1lHiLHOAcbprmsJsohzxgd8Q3Fso1x4Jtl5uVImo4QcvQzJb6iMbjJojsW-8M4pcAp4RAczmGKfN6Wah8ov2NnHsdM71_GS_bz--3Dzapa3_-4u_m6rpzSCirja7TSeGgG6TuUapCCxICABN6qDp0BpwxIpaFR3lpTk3VD3XkBrdVKXbLPJ-8-TU8L5bnfhexoHDHStOReNqA7KYQ0Bf30D_o4LSmW2xVKGd22ujsKv5yo8vKcE_l-n8IO06EH0R9z6EsO_e8cCvvxxbjYHQ1_yT8fX4DrE_AcRjr839Svbtcn5S9H5ZMO</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2637588593</pqid></control><display><type>article</type><title>Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies</title><source>Wiley</source><creator>Wang, Lingling ; Yao, Haobin ; Tong, Teresa ; Lau, KamShing ; Leung, Suet Yi ; Ho, Joshua W. K. ; Leung, Wai K.</creator><creatorcontrib>Wang, Lingling ; Yao, Haobin ; Tong, Teresa ; Lau, KamShing ; Leung, Suet Yi ; Ho, Joshua W. K. ; Leung, Wai K.</creatorcontrib><description>Background Short‐term antibiotics exposure is associated with alterations in microbiota and antibiotic resistance genes (ARGs) in the human gut. While antibiotics are critical in the successful eradication of Helicobacter pylori, the short‐term and long‐term impacts on the composition and quantity of antibiotics resistance genes after H. pylori eradication are unclear. This study used whole‐genome shotgun metagenomic of stool samples to characterize the gut microbiota and ARGs, before and after H. pylori eradication therapy. Results Forty‐four H. pylori‐infected patients were recruited, including 21 treatment naïve patients who received clarithromycin‐based triple therapy (CLA group) and 23 patients who failed previous therapies, in which 10 received levofloxacin‐based quadruple therapy (LEVO group) and 13 received other combinations (OTHER group). Stool samples were collected at baseline (before current treatment), 6 week and 6 month after eradication therapy. At baseline, there was only a slight difference among the three groups on ARGs and gut microbiota. After eradication therapy, there was a transient but significant increase in gut ARGs 6 week post‐therapy, among which the LEVO group had the most significant ARGs alteration compared to other two groups. For treatment naïve patients, those with higher ErmF abundance were prone to fail CLA eradication and gain more ARGs after treatment. For gut microbiota, the bacteria richness decreased at 6 week and there was a significant difference in microbiota community among the three groups at 6 week. Conclusions Our findings demonstrated the dynamic alterations in gut microbiota and ARGs induced by different eradication therapies, which could influence the choices of antibiotics in eradication therapy.</description><identifier>ISSN: 1083-4389</identifier><identifier>EISSN: 1523-5378</identifier><identifier>DOI: 10.1111/hel.12871</identifier><identifier>PMID: 34969161</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Amoxicillin - therapeutic use ; Anti-Bacterial Agents - pharmacology ; Anti-Bacterial Agents - therapeutic use ; Antibiotic resistance ; antibiotic resistance genes ; Antibiotics ; Clarithromycin ; Clarithromycin - pharmacology ; Clarithromycin - therapeutic use ; Drug resistance ; Drug Resistance, Microbial ; Drug Therapy, Combination ; Eradication ; Gastrointestinal Microbiome - genetics ; Genes ; Genomes ; gut microbiota ; Helicobacter Infections - microbiology ; Helicobacter pylori ; Helicobacter pylori - genetics ; Helicobacter pylori eradication ; Humans ; Intestinal microflora ; Levofloxacin ; metagenomic sequencing ; Metagenomics ; Microbiota ; Patients ; short‐chain fatty acid ; Therapy</subject><ispartof>Helicobacter (Cambridge, Mass.), 2022-04, Vol.27 (2), p.e12871-n/a</ispartof><rights>2021 John Wiley &amp; Sons Ltd</rights><rights>2021 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2022 John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533</citedby><cites>FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533</cites><orcidid>0000-0002-5993-1059 ; 0000-0002-9759-7274</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34969161$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Lingling</creatorcontrib><creatorcontrib>Yao, Haobin</creatorcontrib><creatorcontrib>Tong, Teresa</creatorcontrib><creatorcontrib>Lau, KamShing</creatorcontrib><creatorcontrib>Leung, Suet Yi</creatorcontrib><creatorcontrib>Ho, Joshua W. K.</creatorcontrib><creatorcontrib>Leung, Wai K.</creatorcontrib><title>Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies</title><title>Helicobacter (Cambridge, Mass.)</title><addtitle>Helicobacter</addtitle><description>Background Short‐term antibiotics exposure is associated with alterations in microbiota and antibiotic resistance genes (ARGs) in the human gut. While antibiotics are critical in the successful eradication of Helicobacter pylori, the short‐term and long‐term impacts on the composition and quantity of antibiotics resistance genes after H. pylori eradication are unclear. This study used whole‐genome shotgun metagenomic of stool samples to characterize the gut microbiota and ARGs, before and after H. pylori eradication therapy. Results Forty‐four H. pylori‐infected patients were recruited, including 21 treatment naïve patients who received clarithromycin‐based triple therapy (CLA group) and 23 patients who failed previous therapies, in which 10 received levofloxacin‐based quadruple therapy (LEVO group) and 13 received other combinations (OTHER group). Stool samples were collected at baseline (before current treatment), 6 week and 6 month after eradication therapy. At baseline, there was only a slight difference among the three groups on ARGs and gut microbiota. After eradication therapy, there was a transient but significant increase in gut ARGs 6 week post‐therapy, among which the LEVO group had the most significant ARGs alteration compared to other two groups. For treatment naïve patients, those with higher ErmF abundance were prone to fail CLA eradication and gain more ARGs after treatment. For gut microbiota, the bacteria richness decreased at 6 week and there was a significant difference in microbiota community among the three groups at 6 week. Conclusions Our findings demonstrated the dynamic alterations in gut microbiota and ARGs induced by different eradication therapies, which could influence the choices of antibiotics in eradication therapy.</description><subject>Amoxicillin - therapeutic use</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Bacterial Agents - therapeutic use</subject><subject>Antibiotic resistance</subject><subject>antibiotic resistance genes</subject><subject>Antibiotics</subject><subject>Clarithromycin</subject><subject>Clarithromycin - pharmacology</subject><subject>Clarithromycin - therapeutic use</subject><subject>Drug resistance</subject><subject>Drug Resistance, Microbial</subject><subject>Drug Therapy, Combination</subject><subject>Eradication</subject><subject>Gastrointestinal Microbiome - genetics</subject><subject>Genes</subject><subject>Genomes</subject><subject>gut microbiota</subject><subject>Helicobacter Infections - microbiology</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - genetics</subject><subject>Helicobacter pylori eradication</subject><subject>Humans</subject><subject>Intestinal microflora</subject><subject>Levofloxacin</subject><subject>metagenomic sequencing</subject><subject>Metagenomics</subject><subject>Microbiota</subject><subject>Patients</subject><subject>short‐chain fatty acid</subject><subject>Therapy</subject><issn>1083-4389</issn><issn>1523-5378</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kUFvFCEUx4mxsbV68AsYEi96mJYHwzBzNLW6TTbppZ4nD-axSzPLbGEmzX57Wbd6MJED8ODHL8CfsQ8grqC06y2NVyBbA6_YBWipKq1M-7rMRauqWrXdOXub86MQQqu6e8POS9900MAFe_p2iLgLjrstxg1lHiLHOAcbprmsJsohzxgd8Q3Fso1x4Jtl5uVImo4QcvQzJb6iMbjJojsW-8M4pcAp4RAczmGKfN6Wah8ov2NnHsdM71_GS_bz--3Dzapa3_-4u_m6rpzSCirja7TSeGgG6TuUapCCxICABN6qDp0BpwxIpaFR3lpTk3VD3XkBrdVKXbLPJ-8-TU8L5bnfhexoHDHStOReNqA7KYQ0Bf30D_o4LSmW2xVKGd22ujsKv5yo8vKcE_l-n8IO06EH0R9z6EsO_e8cCvvxxbjYHQ1_yT8fX4DrE_AcRjr839Svbtcn5S9H5ZMO</recordid><startdate>202204</startdate><enddate>202204</enddate><creator>Wang, Lingling</creator><creator>Yao, Haobin</creator><creator>Tong, Teresa</creator><creator>Lau, KamShing</creator><creator>Leung, Suet Yi</creator><creator>Ho, Joshua W. K.</creator><creator>Leung, Wai K.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5993-1059</orcidid><orcidid>https://orcid.org/0000-0002-9759-7274</orcidid></search><sort><creationdate>202204</creationdate><title>Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies</title><author>Wang, Lingling ; Yao, Haobin ; Tong, Teresa ; Lau, KamShing ; Leung, Suet Yi ; Ho, Joshua W. K. ; Leung, Wai K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amoxicillin - therapeutic use</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>Antibiotic resistance</topic><topic>antibiotic resistance genes</topic><topic>Antibiotics</topic><topic>Clarithromycin</topic><topic>Clarithromycin - pharmacology</topic><topic>Clarithromycin - therapeutic use</topic><topic>Drug resistance</topic><topic>Drug Resistance, Microbial</topic><topic>Drug Therapy, Combination</topic><topic>Eradication</topic><topic>Gastrointestinal Microbiome - genetics</topic><topic>Genes</topic><topic>Genomes</topic><topic>gut microbiota</topic><topic>Helicobacter Infections - microbiology</topic><topic>Helicobacter pylori</topic><topic>Helicobacter pylori - genetics</topic><topic>Helicobacter pylori eradication</topic><topic>Humans</topic><topic>Intestinal microflora</topic><topic>Levofloxacin</topic><topic>metagenomic sequencing</topic><topic>Metagenomics</topic><topic>Microbiota</topic><topic>Patients</topic><topic>short‐chain fatty acid</topic><topic>Therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Lingling</creatorcontrib><creatorcontrib>Yao, Haobin</creatorcontrib><creatorcontrib>Tong, Teresa</creatorcontrib><creatorcontrib>Lau, KamShing</creatorcontrib><creatorcontrib>Leung, Suet Yi</creatorcontrib><creatorcontrib>Ho, Joshua W. K.</creatorcontrib><creatorcontrib>Leung, Wai K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Helicobacter (Cambridge, Mass.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Lingling</au><au>Yao, Haobin</au><au>Tong, Teresa</au><au>Lau, KamShing</au><au>Leung, Suet Yi</au><au>Ho, Joshua W. K.</au><au>Leung, Wai K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies</atitle><jtitle>Helicobacter (Cambridge, Mass.)</jtitle><addtitle>Helicobacter</addtitle><date>2022-04</date><risdate>2022</risdate><volume>27</volume><issue>2</issue><spage>e12871</spage><epage>n/a</epage><pages>e12871-n/a</pages><issn>1083-4389</issn><eissn>1523-5378</eissn><abstract>Background Short‐term antibiotics exposure is associated with alterations in microbiota and antibiotic resistance genes (ARGs) in the human gut. While antibiotics are critical in the successful eradication of Helicobacter pylori, the short‐term and long‐term impacts on the composition and quantity of antibiotics resistance genes after H. pylori eradication are unclear. This study used whole‐genome shotgun metagenomic of stool samples to characterize the gut microbiota and ARGs, before and after H. pylori eradication therapy. Results Forty‐four H. pylori‐infected patients were recruited, including 21 treatment naïve patients who received clarithromycin‐based triple therapy (CLA group) and 23 patients who failed previous therapies, in which 10 received levofloxacin‐based quadruple therapy (LEVO group) and 13 received other combinations (OTHER group). Stool samples were collected at baseline (before current treatment), 6 week and 6 month after eradication therapy. At baseline, there was only a slight difference among the three groups on ARGs and gut microbiota. After eradication therapy, there was a transient but significant increase in gut ARGs 6 week post‐therapy, among which the LEVO group had the most significant ARGs alteration compared to other two groups. For treatment naïve patients, those with higher ErmF abundance were prone to fail CLA eradication and gain more ARGs after treatment. For gut microbiota, the bacteria richness decreased at 6 week and there was a significant difference in microbiota community among the three groups at 6 week. Conclusions Our findings demonstrated the dynamic alterations in gut microbiota and ARGs induced by different eradication therapies, which could influence the choices of antibiotics in eradication therapy.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34969161</pmid><doi>10.1111/hel.12871</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-5993-1059</orcidid><orcidid>https://orcid.org/0000-0002-9759-7274</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1083-4389
ispartof Helicobacter (Cambridge, Mass.), 2022-04, Vol.27 (2), p.e12871-n/a
issn 1083-4389
1523-5378
language eng
recordid cdi_proquest_miscellaneous_2615920027
source Wiley
subjects Amoxicillin - therapeutic use
Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - therapeutic use
Antibiotic resistance
antibiotic resistance genes
Antibiotics
Clarithromycin
Clarithromycin - pharmacology
Clarithromycin - therapeutic use
Drug resistance
Drug Resistance, Microbial
Drug Therapy, Combination
Eradication
Gastrointestinal Microbiome - genetics
Genes
Genomes
gut microbiota
Helicobacter Infections - microbiology
Helicobacter pylori
Helicobacter pylori - genetics
Helicobacter pylori eradication
Humans
Intestinal microflora
Levofloxacin
metagenomic sequencing
Metagenomics
Microbiota
Patients
short‐chain fatty acid
Therapy
title Dynamic changes in antibiotic resistance genes and gut microbiota after Helicobacter pylori eradication therapies
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T04%3A38%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dynamic%20changes%20in%20antibiotic%20resistance%20genes%20and%20gut%20microbiota%20after%20Helicobacter%20pylori%20eradication%20therapies&rft.jtitle=Helicobacter%20(Cambridge,%20Mass.)&rft.au=Wang,%20Lingling&rft.date=2022-04&rft.volume=27&rft.issue=2&rft.spage=e12871&rft.epage=n/a&rft.pages=e12871-n/a&rft.issn=1083-4389&rft.eissn=1523-5378&rft_id=info:doi/10.1111/hel.12871&rft_dat=%3Cproquest_cross%3E2615920027%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3531-7f4ab27f16d2f9a23d20e0da1ae1fb39ac71c371235163fbb74ebcd49f018b533%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2637588593&rft_id=info:pmid/34969161&rfr_iscdi=true