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A fatal case of peritonitis caused by Dysgonomonas capnocytophagoides harboring the novel metallo-beta-lactamase gene blaDYB-1
•Dysgonomonas capnocytophagoides rarely causes an opportunistic infection.•Treatment of D. capnocytophagoides is challenging due to the multidrug resistance.•We report a fatal case of peritonitis caused by D. capnocytophagoides in Japan.•We detected a novel metallo-beta-lactamase gene (blaDYB-1) in...
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Published in: | International journal of infectious diseases 2024-10, Vol.147, p.107174, Article 107174 |
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container_title | International journal of infectious diseases |
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creator | Imai, Kazuo Kodana, Masahiro Omachi, Ryuha Inoue, Tsutomu Okada, Hirokazu Maeda, Takuya |
description | •Dysgonomonas capnocytophagoides rarely causes an opportunistic infection.•Treatment of D. capnocytophagoides is challenging due to the multidrug resistance.•We report a fatal case of peritonitis caused by D. capnocytophagoides in Japan.•We detected a novel metallo-beta-lactamase gene (blaDYB-1) in the isolate.
Dysgonomonas capnocytophagoides shows multidrug resistance to antibiotics and causes opportunistic infections in immunocompromised hosts. The drug resistance mechanisms of D. capnocytophagoides have not yet been identified. In this work, we analyzed D. capnocytophagoides isolated from a fatal case of peritonitis to clarify its drug resistance mechanisms. Whole genome sequencing revealed that our isolate harbored a chromosomally encoded metallo-beta-lactamase (designated blaDYB-1) and a chromosomally encoded ermFS gene. Phylogenetic analysis, primary sequence comparison, and structural modeling analysis of DYB-1 showed it was highly similar to CfiA in Bacteroides fragilis and belonged to the B1 MBL family. Transformation analysis into Escherichia coli TOP10 showed that a recombinant plasmid containing blaDYB-1 increased the minimum inhibitory concentration of beta-lactams, including carbapenem. We identified a novel chromosomally encoded class B1 metallo-beta-lactamase gene designated blaDYB-1 and an ermFS gene that contributed to multidrug resistance. This study indicates the importance of further surveillance for D. capnocytophagoides harboring blaDYB-1. |
doi_str_mv | 10.1016/j.ijid.2024.107174 |
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Dysgonomonas capnocytophagoides shows multidrug resistance to antibiotics and causes opportunistic infections in immunocompromised hosts. The drug resistance mechanisms of D. capnocytophagoides have not yet been identified. In this work, we analyzed D. capnocytophagoides isolated from a fatal case of peritonitis to clarify its drug resistance mechanisms. Whole genome sequencing revealed that our isolate harbored a chromosomally encoded metallo-beta-lactamase (designated blaDYB-1) and a chromosomally encoded ermFS gene. Phylogenetic analysis, primary sequence comparison, and structural modeling analysis of DYB-1 showed it was highly similar to CfiA in Bacteroides fragilis and belonged to the B1 MBL family. Transformation analysis into Escherichia coli TOP10 showed that a recombinant plasmid containing blaDYB-1 increased the minimum inhibitory concentration of beta-lactams, including carbapenem. We identified a novel chromosomally encoded class B1 metallo-beta-lactamase gene designated blaDYB-1 and an ermFS gene that contributed to multidrug resistance. This study indicates the importance of further surveillance for D. capnocytophagoides harboring blaDYB-1.</description><identifier>ISSN: 1201-9712</identifier><identifier>ISSN: 1878-3511</identifier><identifier>EISSN: 1878-3511</identifier><identifier>DOI: 10.1016/j.ijid.2024.107174</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Dysgonomonas capnocytophagoides ; Metallo-beta-lactamase ; Multidrug resistance ; Whole genome sequencing</subject><ispartof>International journal of infectious diseases, 2024-10, Vol.147, p.107174, Article 107174</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-8416-7371</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1201971224002455$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3536,27905,27906,45761</link.rule.ids></links><search><creatorcontrib>Imai, Kazuo</creatorcontrib><creatorcontrib>Kodana, Masahiro</creatorcontrib><creatorcontrib>Omachi, Ryuha</creatorcontrib><creatorcontrib>Inoue, Tsutomu</creatorcontrib><creatorcontrib>Okada, Hirokazu</creatorcontrib><creatorcontrib>Maeda, Takuya</creatorcontrib><title>A fatal case of peritonitis caused by Dysgonomonas capnocytophagoides harboring the novel metallo-beta-lactamase gene blaDYB-1</title><title>International journal of infectious diseases</title><description>•Dysgonomonas capnocytophagoides rarely causes an opportunistic infection.•Treatment of D. capnocytophagoides is challenging due to the multidrug resistance.•We report a fatal case of peritonitis caused by D. capnocytophagoides in Japan.•We detected a novel metallo-beta-lactamase gene (blaDYB-1) in the isolate.
Dysgonomonas capnocytophagoides shows multidrug resistance to antibiotics and causes opportunistic infections in immunocompromised hosts. The drug resistance mechanisms of D. capnocytophagoides have not yet been identified. In this work, we analyzed D. capnocytophagoides isolated from a fatal case of peritonitis to clarify its drug resistance mechanisms. Whole genome sequencing revealed that our isolate harbored a chromosomally encoded metallo-beta-lactamase (designated blaDYB-1) and a chromosomally encoded ermFS gene. Phylogenetic analysis, primary sequence comparison, and structural modeling analysis of DYB-1 showed it was highly similar to CfiA in Bacteroides fragilis and belonged to the B1 MBL family. Transformation analysis into Escherichia coli TOP10 showed that a recombinant plasmid containing blaDYB-1 increased the minimum inhibitory concentration of beta-lactams, including carbapenem. We identified a novel chromosomally encoded class B1 metallo-beta-lactamase gene designated blaDYB-1 and an ermFS gene that contributed to multidrug resistance. This study indicates the importance of further surveillance for D. capnocytophagoides harboring blaDYB-1.</description><subject>Dysgonomonas capnocytophagoides</subject><subject>Metallo-beta-lactamase</subject><subject>Multidrug resistance</subject><subject>Whole genome sequencing</subject><issn>1201-9712</issn><issn>1878-3511</issn><issn>1878-3511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNotkUFv1DAUhCMEEqXwBzj5yCWL7cR2InEpbaGVKvUCB07Ws_2cdZTEwc5W2gu_HYflNE-fRjN6mqr6yOiBUSY_j4cwBnfglLcFKKbaV9UV61RXN4Kx1-XmlNW9Yvxt9S7nkVLaStldVX9uiIcNJmIhI4merJjCFpewhVzYKaMj5kzuznmIS5zjAjtel2jPW1yPMMTgMJMjJBNTWAayHZEs8QUnMmPJnWJtitYT2A3mvWPABYmZ4O7X15q9r954mDJ--K_X1c9v9z9uH-qn5--PtzdPtWOCt7VQvAffc9ugQ0e5p1KpnnsjUXJBqZINE10BshXcGcV6QQ1znTSCgpCqua4eL7kuwqjXFGZIZx0h6H8gpkFD2oKdUKPvrBe9NZJCyyUAdLa33jG0AozvStanS9aa4u8T5k3PIVucJlgwnrJuaMd4T6Vsi_XLxYrlt5eASWcbcLHoQkK7lfKgGdX7hHrU-4R6n1BfJmz-AhGWkj8</recordid><startdate>202410</startdate><enddate>202410</enddate><creator>Imai, Kazuo</creator><creator>Kodana, Masahiro</creator><creator>Omachi, Ryuha</creator><creator>Inoue, Tsutomu</creator><creator>Okada, Hirokazu</creator><creator>Maeda, Takuya</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-8416-7371</orcidid></search><sort><creationdate>202410</creationdate><title>A fatal case of peritonitis caused by Dysgonomonas capnocytophagoides harboring the novel metallo-beta-lactamase gene blaDYB-1</title><author>Imai, Kazuo ; Kodana, Masahiro ; Omachi, Ryuha ; Inoue, Tsutomu ; Okada, Hirokazu ; Maeda, Takuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d1524-5729af92c3eded02f067792fb6e6250076315892f6452db71950b1d86b50a5673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Dysgonomonas capnocytophagoides</topic><topic>Metallo-beta-lactamase</topic><topic>Multidrug resistance</topic><topic>Whole genome sequencing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Imai, Kazuo</creatorcontrib><creatorcontrib>Kodana, Masahiro</creatorcontrib><creatorcontrib>Omachi, Ryuha</creatorcontrib><creatorcontrib>Inoue, Tsutomu</creatorcontrib><creatorcontrib>Okada, Hirokazu</creatorcontrib><creatorcontrib>Maeda, Takuya</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imai, Kazuo</au><au>Kodana, Masahiro</au><au>Omachi, Ryuha</au><au>Inoue, Tsutomu</au><au>Okada, Hirokazu</au><au>Maeda, Takuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A fatal case of peritonitis caused by Dysgonomonas capnocytophagoides harboring the novel metallo-beta-lactamase gene blaDYB-1</atitle><jtitle>International journal of infectious diseases</jtitle><date>2024-10</date><risdate>2024</risdate><volume>147</volume><spage>107174</spage><pages>107174-</pages><artnum>107174</artnum><issn>1201-9712</issn><issn>1878-3511</issn><eissn>1878-3511</eissn><abstract>•Dysgonomonas capnocytophagoides rarely causes an opportunistic infection.•Treatment of D. capnocytophagoides is challenging due to the multidrug resistance.•We report a fatal case of peritonitis caused by D. capnocytophagoides in Japan.•We detected a novel metallo-beta-lactamase gene (blaDYB-1) in the isolate.
Dysgonomonas capnocytophagoides shows multidrug resistance to antibiotics and causes opportunistic infections in immunocompromised hosts. The drug resistance mechanisms of D. capnocytophagoides have not yet been identified. In this work, we analyzed D. capnocytophagoides isolated from a fatal case of peritonitis to clarify its drug resistance mechanisms. Whole genome sequencing revealed that our isolate harbored a chromosomally encoded metallo-beta-lactamase (designated blaDYB-1) and a chromosomally encoded ermFS gene. Phylogenetic analysis, primary sequence comparison, and structural modeling analysis of DYB-1 showed it was highly similar to CfiA in Bacteroides fragilis and belonged to the B1 MBL family. Transformation analysis into Escherichia coli TOP10 showed that a recombinant plasmid containing blaDYB-1 increased the minimum inhibitory concentration of beta-lactams, including carbapenem. We identified a novel chromosomally encoded class B1 metallo-beta-lactamase gene designated blaDYB-1 and an ermFS gene that contributed to multidrug resistance. This study indicates the importance of further surveillance for D. capnocytophagoides harboring blaDYB-1.</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.ijid.2024.107174</doi><orcidid>https://orcid.org/0000-0002-8416-7371</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Dysgonomonas capnocytophagoides Metallo-beta-lactamase Multidrug resistance Whole genome sequencing |
title | A fatal case of peritonitis caused by Dysgonomonas capnocytophagoides harboring the novel metallo-beta-lactamase gene blaDYB-1 |
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