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The global distribution of the macrolide esterase EstX from the alpha/beta hydrolase superfamily
Macrolide antibiotics, pivotal in clinical therapeutics, are confronting resistance challenges mediated by enzymes like macrolide esterases, which are classified into Ere-type and the less studied Est-type. In this study, we provide the biochemical confirmation of EstX, an Est-type macrolide esteras...
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Published in: | Communications biology 2024-06, Vol.7 (1), p.781-12, Article 781 |
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creator | Lin, Jiafu Lv, Hua Wang, Tiantian Tao, Hongkun Zhong, Yi Zhou, Yang Tang, Yibo Xie, Feng Zhuang, Guoqing Xu, Changwen Chu, Yiwen Wang, Xinrong Yang, Yongqiang Song, Tao |
description | Macrolide antibiotics, pivotal in clinical therapeutics, are confronting resistance challenges mediated by enzymes like macrolide esterases, which are classified into Ere-type and the less studied Est-type. In this study, we provide the biochemical confirmation of EstX, an Est-type macrolide esterase that initially identified as unknown protein in the 1980s. EstX is capable of hydrolyzing four 16-membered ring macrolides, encompassing both veterinary (tylosin, tidipirosin, and tilmicosin) and human-use (leucomycin A5) antibiotics. It uses typical catalytic triad (Asp233-His261-Ser102) from alpha/beta hydrolase superfamily for ester bond hydrolysis. Further genomic context analysis suggests that the dissemination of
estX
is likely facilitated by mobile genetic elements such as integrons and transposons. The global distribution study indicates that bacteria harboring the
estX
gene, predominantly pathogenic species like
Escherichia coli
,
Salmonella enterica
, and
Klebsiella pneumoniae
, are prevalent in 74 countries across 6 continents. Additionally, the emergence timeline of the
estX
gene suggests its proliferation may be linked to the overuse of macrolide antibiotics. The widespread prevalence and dissemination of Est-type macrolide esterase highlight an urgent need for enhanced monitoring and in-depth research, underlining its significance as an escalating public health issue.
Macrolide esterase EstX can degrade both veterinary and human-use 16-membered ring macrolides. This enzyme is widely distributed among pathogenic species and across 74 countries on 6 continents,with its dissemination likely facilitated by integrons and transposons. |
doi_str_mv | 10.1038/s42003-024-06473-2 |
format | article |
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estX
is likely facilitated by mobile genetic elements such as integrons and transposons. The global distribution study indicates that bacteria harboring the
estX
gene, predominantly pathogenic species like
Escherichia coli
,
Salmonella enterica
, and
Klebsiella pneumoniae
, are prevalent in 74 countries across 6 continents. Additionally, the emergence timeline of the
estX
gene suggests its proliferation may be linked to the overuse of macrolide antibiotics. The widespread prevalence and dissemination of Est-type macrolide esterase highlight an urgent need for enhanced monitoring and in-depth research, underlining its significance as an escalating public health issue.
Macrolide esterase EstX can degrade both veterinary and human-use 16-membered ring macrolides. This enzyme is widely distributed among pathogenic species and across 74 countries on 6 continents,with its dissemination likely facilitated by integrons and transposons.</description><identifier>ISSN: 2399-3642</identifier><identifier>EISSN: 2399-3642</identifier><identifier>DOI: 10.1038/s42003-024-06473-2</identifier><identifier>PMID: 38944651</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326 ; 631/337 ; 631/45 ; 82/16 ; 82/80 ; 82/83 ; Anti-Bacterial Agents - metabolism ; Anti-Bacterial Agents - pharmacology ; Bacterial Proteins - chemistry ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biomedical and Life Sciences ; Esterases - chemistry ; Esterases - genetics ; Esterases - metabolism ; Humans ; Hydrolases - chemistry ; Hydrolases - genetics ; Hydrolases - metabolism ; Life Sciences ; Macrolides - metabolism ; Phylogeny</subject><ispartof>Communications biology, 2024-06, Vol.7 (1), p.781-12, Article 781</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c394t-fb9871b4971577d0d312dcfd1020c425eb43d6f8dbbdd172847fa5bb9091a1023</cites><orcidid>0000-0002-0246-0372 ; 0000-0003-1554-3828</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11214618/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11214618/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,36992,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38944651$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Jiafu</creatorcontrib><creatorcontrib>Lv, Hua</creatorcontrib><creatorcontrib>Wang, Tiantian</creatorcontrib><creatorcontrib>Tao, Hongkun</creatorcontrib><creatorcontrib>Zhong, Yi</creatorcontrib><creatorcontrib>Zhou, Yang</creatorcontrib><creatorcontrib>Tang, Yibo</creatorcontrib><creatorcontrib>Xie, Feng</creatorcontrib><creatorcontrib>Zhuang, Guoqing</creatorcontrib><creatorcontrib>Xu, Changwen</creatorcontrib><creatorcontrib>Chu, Yiwen</creatorcontrib><creatorcontrib>Wang, Xinrong</creatorcontrib><creatorcontrib>Yang, Yongqiang</creatorcontrib><creatorcontrib>Song, Tao</creatorcontrib><title>The global distribution of the macrolide esterase EstX from the alpha/beta hydrolase superfamily</title><title>Communications biology</title><addtitle>Commun Biol</addtitle><addtitle>Commun Biol</addtitle><description>Macrolide antibiotics, pivotal in clinical therapeutics, are confronting resistance challenges mediated by enzymes like macrolide esterases, which are classified into Ere-type and the less studied Est-type. In this study, we provide the biochemical confirmation of EstX, an Est-type macrolide esterase that initially identified as unknown protein in the 1980s. EstX is capable of hydrolyzing four 16-membered ring macrolides, encompassing both veterinary (tylosin, tidipirosin, and tilmicosin) and human-use (leucomycin A5) antibiotics. It uses typical catalytic triad (Asp233-His261-Ser102) from alpha/beta hydrolase superfamily for ester bond hydrolysis. Further genomic context analysis suggests that the dissemination of
estX
is likely facilitated by mobile genetic elements such as integrons and transposons. The global distribution study indicates that bacteria harboring the
estX
gene, predominantly pathogenic species like
Escherichia coli
,
Salmonella enterica
, and
Klebsiella pneumoniae
, are prevalent in 74 countries across 6 continents. Additionally, the emergence timeline of the
estX
gene suggests its proliferation may be linked to the overuse of macrolide antibiotics. The widespread prevalence and dissemination of Est-type macrolide esterase highlight an urgent need for enhanced monitoring and in-depth research, underlining its significance as an escalating public health issue.
Macrolide esterase EstX can degrade both veterinary and human-use 16-membered ring macrolides. This enzyme is widely distributed among pathogenic species and across 74 countries on 6 continents,with its dissemination likely facilitated by integrons and transposons.</description><subject>631/326</subject><subject>631/337</subject><subject>631/45</subject><subject>82/16</subject><subject>82/80</subject><subject>82/83</subject><subject>Anti-Bacterial Agents - metabolism</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Esterases - chemistry</subject><subject>Esterases - genetics</subject><subject>Esterases - metabolism</subject><subject>Humans</subject><subject>Hydrolases - chemistry</subject><subject>Hydrolases - genetics</subject><subject>Hydrolases - metabolism</subject><subject>Life Sciences</subject><subject>Macrolides - metabolism</subject><subject>Phylogeny</subject><issn>2399-3642</issn><issn>2399-3642</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kc1u1DAUhS0EolXpC7BAWbIJ9V_ieIVQVaBSJTZFYmeuY3vGIycebAdp3r6eSanaDStbPud-vjoHofcEfyKYDVeZU4xZiylvcc8Fa-krdE6ZlC3rOX397H6GLnPeYYyJlLJn_C06Y4PkvO_IOfp9v7XNJkQNoTE-l-T1Unycm-iaUqUJxhSDN7axudgE2TY3ufxqXIrTyQBhv4UrbQs024Op3qMlL3ubHEw-HN6hNw5CtpeP5wX6-fXm_vp7e_fj2-31l7t2ZJKX1mk5CKK5FKQTwmDDCDWjMwRTPHLaWc2Z6d1gtDaGCDpw4aDTWmJJoJrYBbpduSbCTu2TnyAdVASvTg8xbRSk4sdglegdFVBZwtYYcC8pcKOhpqMNkLGrrM8ra7_oyZrRziVBeAF9qcx-qzbxryKEEt6ToRI-PhJS_LPU6NTk82hDgNnGJSuGBROESXJcnK7WGnTOybqnfwhWx6rVWrWqVatT1eo49OH5hk8j_4qtBrYacpXmjU1qF5c01wb-h30Asd-1xw</recordid><startdate>20240628</startdate><enddate>20240628</enddate><creator>Lin, Jiafu</creator><creator>Lv, Hua</creator><creator>Wang, Tiantian</creator><creator>Tao, Hongkun</creator><creator>Zhong, Yi</creator><creator>Zhou, Yang</creator><creator>Tang, Yibo</creator><creator>Xie, Feng</creator><creator>Zhuang, Guoqing</creator><creator>Xu, Changwen</creator><creator>Chu, Yiwen</creator><creator>Wang, Xinrong</creator><creator>Yang, Yongqiang</creator><creator>Song, Tao</creator><general>Nature Publishing Group UK</general><general>Nature Portfolio</general><scope>C6C</scope><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>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0246-0372</orcidid><orcidid>https://orcid.org/0000-0003-1554-3828</orcidid></search><sort><creationdate>20240628</creationdate><title>The global distribution of the macrolide esterase EstX from the alpha/beta hydrolase superfamily</title><author>Lin, Jiafu ; 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In this study, we provide the biochemical confirmation of EstX, an Est-type macrolide esterase that initially identified as unknown protein in the 1980s. EstX is capable of hydrolyzing four 16-membered ring macrolides, encompassing both veterinary (tylosin, tidipirosin, and tilmicosin) and human-use (leucomycin A5) antibiotics. It uses typical catalytic triad (Asp233-His261-Ser102) from alpha/beta hydrolase superfamily for ester bond hydrolysis. Further genomic context analysis suggests that the dissemination of
estX
is likely facilitated by mobile genetic elements such as integrons and transposons. The global distribution study indicates that bacteria harboring the
estX
gene, predominantly pathogenic species like
Escherichia coli
,
Salmonella enterica
, and
Klebsiella pneumoniae
, are prevalent in 74 countries across 6 continents. Additionally, the emergence timeline of the
estX
gene suggests its proliferation may be linked to the overuse of macrolide antibiotics. The widespread prevalence and dissemination of Est-type macrolide esterase highlight an urgent need for enhanced monitoring and in-depth research, underlining its significance as an escalating public health issue.
Macrolide esterase EstX can degrade both veterinary and human-use 16-membered ring macrolides. This enzyme is widely distributed among pathogenic species and across 74 countries on 6 continents,with its dissemination likely facilitated by integrons and transposons.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>38944651</pmid><doi>10.1038/s42003-024-06473-2</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0246-0372</orcidid><orcidid>https://orcid.org/0000-0003-1554-3828</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 631/326 631/337 631/45 82/16 82/80 82/83 Anti-Bacterial Agents - metabolism Anti-Bacterial Agents - pharmacology Bacterial Proteins - chemistry Bacterial Proteins - genetics Bacterial Proteins - metabolism Biomedical and Life Sciences Esterases - chemistry Esterases - genetics Esterases - metabolism Humans Hydrolases - chemistry Hydrolases - genetics Hydrolases - metabolism Life Sciences Macrolides - metabolism Phylogeny |
title | The global distribution of the macrolide esterase EstX from the alpha/beta hydrolase superfamily |
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