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CTX-M-15 Positive Escherichia coli and Klebsiella pneumoniae Outbreak in the Neonatal Intensive Care Unit of a Maternity Hospital in Ha’il, Saudi Arabia
Objective: The aim of this study was to retrospectively characterize E. coli and K. pneumoniae isolates obtained from neonates during a suspected NICU outbreak of infection in Ha'il, Saudi Arabia during a period of one month (April 2014). Methods: Antibiotic susceptibility patterns, molecular c...
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Published in: | Infection and drug resistance 2021-01, Vol.14, p.2843-2849 |
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creator | Almogbel, Mohammed Altheban, Ahmed Alenezi, Mohammed Motair, Khalid Al Menezes, Godfred A Elabbasy, Mohammed Hammam, Sahar Hays, John P Khan, Mushtaq A |
description | Objective: The aim of this study was to retrospectively characterize E. coli and K. pneumoniae isolates obtained from neonates during a suspected NICU outbreak of infection in Ha'il, Saudi Arabia during a period of one month (April 2014). Methods: Antibiotic susceptibility patterns, molecular characterization for antibiotic-resistant genes (blaTEM, blaSHV, and blaCTX-M), and genotyping by PFGE and MLST were performed. Results: A total of 24 E. coli and 48 K. pneumoniae isolates were cultured from neonates that had been admitted to the NICU. Among E. coli, the majority of isolates (19/24) were ESBL-positive and all of these nineteen (100%) harbored the CTX-M-15 gene. A total of 15% (3/19) were co-producers of CTX-M-15 and SHV-12, and 68.4% (13/19) were co-producers of CTX-M-15 and TEM-1. Among K. pneumoniae isolates, 87.5% (42/48) were ESBL positive with 92.85% (39/42) of these isolates containing the CTX-M-15 gene. A total of 97% (38/39) of K. pneumoniae were co-producers of CTX-M-15 and SHV-12, and 88% (37/42) were positive for TEM-1. Furthermore, 85.7% (36/42) K. pneumoniae were co-producers of CTX-M-15 and TEM-1. The majority of E. coli isolates (18/19 isolates) were grouped into two genetic clusters by pulsed field gel electrophoresis (PFGE) and all the isolates were found to be ST-131 type. In contrast, K. pneumoniae (31/42) isolates belonged to a single genotypic lineage, and all (100%) isolates belonged to the ST-14 type. Conclusion: This is the first report of CTX-M-15-positive, ESBL E. coli, and K. pneumoniae isolates recovered from an outbreak in an NICU in Ha'il, Saudi Arabia. It is alarming to note the high rate of outbreak isolates with simultaneous production of CTX-M-15 and SHV-12 conferring high-level resistance to oxyimino-cephalosporins. Keywords: extended spectrum [beta]-lactamases, NICU outbreak, CTX-M-15, E. coli, K. pneumoniae |
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Methods: Antibiotic susceptibility patterns, molecular characterization for antibiotic-resistant genes (blaTEM, blaSHV, and blaCTX-M), and genotyping by PFGE and MLST were performed. Results: A total of 24 E. coli and 48 K. pneumoniae isolates were cultured from neonates that had been admitted to the NICU. Among E. coli, the majority of isolates (19/24) were ESBL-positive and all of these nineteen (100%) harbored the CTX-M-15 gene. A total of 15% (3/19) were co-producers of CTX-M-15 and SHV-12, and 68.4% (13/19) were co-producers of CTX-M-15 and TEM-1. Among K. pneumoniae isolates, 87.5% (42/48) were ESBL positive with 92.85% (39/42) of these isolates containing the CTX-M-15 gene. A total of 97% (38/39) of K. pneumoniae were co-producers of CTX-M-15 and SHV-12, and 88% (37/42) were positive for TEM-1. Furthermore, 85.7% (36/42) K. pneumoniae were co-producers of CTX-M-15 and TEM-1. The majority of E. coli isolates (18/19 isolates) were grouped into two genetic clusters by pulsed field gel electrophoresis (PFGE) and all the isolates were found to be ST-131 type. In contrast, K. pneumoniae (31/42) isolates belonged to a single genotypic lineage, and all (100%) isolates belonged to the ST-14 type. Conclusion: This is the first report of CTX-M-15-positive, ESBL E. coli, and K. pneumoniae isolates recovered from an outbreak in an NICU in Ha'il, Saudi Arabia. It is alarming to note the high rate of outbreak isolates with simultaneous production of CTX-M-15 and SHV-12 conferring high-level resistance to oxyimino-cephalosporins. Keywords: extended spectrum [beta]-lactamases, NICU outbreak, CTX-M-15, E. coli, K. pneumoniae</description><identifier>ISSN: 1178-6973</identifier><identifier>EISSN: 1178-6973</identifier><identifier>DOI: 10.2147/IDR.S317079</identifier><identifier>PMID: 34326652</identifier><language>eng</language><publisher>Macclesfield: Dove Medical Press Limited</publisher><subject>Antibiotic resistance ; Antibiotics ; Bacterial infections ; Bacterial pneumonia ; Beta lactamases ; Cephalosporins ; Cluster analysis ; ctx-m-15 ; E coli ; Enzymes ; Epidemics ; Escherichia coli ; extended spectrum beta lactamases ; Gel electrophoresis ; Genes ; Genetic aspects ; Genotyping ; Imipenem ; Infants (Newborn) ; Infections ; Intensive care ; k. pneumoniae ; Medical personnel ; Neonatal intensive care ; Neonates ; nicu outbreak ; Original Research ; Outbreaks ; Pneumonia</subject><ispartof>Infection and drug resistance, 2021-01, Vol.14, p.2843-2849</ispartof><rights>COPYRIGHT 2021 Dove Medical Press Limited</rights><rights>2021. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Almogbel et al. 2021 Almogbel et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-644c2e7e81eb015c506994f08a0ab484e69988665ff5282a3c0679c0ccf95ada3</citedby><cites>FETCH-LOGICAL-c550t-644c2e7e81eb015c506994f08a0ab484e69988665ff5282a3c0679c0ccf95ada3</cites><orcidid>0000-0001-9183-4497 ; 0000-0002-2434-1411</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2557122394/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2557122394?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids></links><search><creatorcontrib>Almogbel, Mohammed</creatorcontrib><creatorcontrib>Altheban, Ahmed</creatorcontrib><creatorcontrib>Alenezi, Mohammed</creatorcontrib><creatorcontrib>Motair, Khalid Al</creatorcontrib><creatorcontrib>Menezes, Godfred A</creatorcontrib><creatorcontrib>Elabbasy, Mohammed</creatorcontrib><creatorcontrib>Hammam, Sahar</creatorcontrib><creatorcontrib>Hays, John P</creatorcontrib><creatorcontrib>Khan, Mushtaq A</creatorcontrib><title>CTX-M-15 Positive Escherichia coli and Klebsiella pneumoniae Outbreak in the Neonatal Intensive Care Unit of a Maternity Hospital in Ha’il, Saudi Arabia</title><title>Infection and drug resistance</title><description>Objective: The aim of this study was to retrospectively characterize E. coli and K. pneumoniae isolates obtained from neonates during a suspected NICU outbreak of infection in Ha'il, Saudi Arabia during a period of one month (April 2014). Methods: Antibiotic susceptibility patterns, molecular characterization for antibiotic-resistant genes (blaTEM, blaSHV, and blaCTX-M), and genotyping by PFGE and MLST were performed. Results: A total of 24 E. coli and 48 K. pneumoniae isolates were cultured from neonates that had been admitted to the NICU. Among E. coli, the majority of isolates (19/24) were ESBL-positive and all of these nineteen (100%) harbored the CTX-M-15 gene. A total of 15% (3/19) were co-producers of CTX-M-15 and SHV-12, and 68.4% (13/19) were co-producers of CTX-M-15 and TEM-1. Among K. pneumoniae isolates, 87.5% (42/48) were ESBL positive with 92.85% (39/42) of these isolates containing the CTX-M-15 gene. A total of 97% (38/39) of K. pneumoniae were co-producers of CTX-M-15 and SHV-12, and 88% (37/42) were positive for TEM-1. Furthermore, 85.7% (36/42) K. pneumoniae were co-producers of CTX-M-15 and TEM-1. The majority of E. coli isolates (18/19 isolates) were grouped into two genetic clusters by pulsed field gel electrophoresis (PFGE) and all the isolates were found to be ST-131 type. In contrast, K. pneumoniae (31/42) isolates belonged to a single genotypic lineage, and all (100%) isolates belonged to the ST-14 type. Conclusion: This is the first report of CTX-M-15-positive, ESBL E. coli, and K. pneumoniae isolates recovered from an outbreak in an NICU in Ha'il, Saudi Arabia. It is alarming to note the high rate of outbreak isolates with simultaneous production of CTX-M-15 and SHV-12 conferring high-level resistance to oxyimino-cephalosporins. Keywords: extended spectrum [beta]-lactamases, NICU outbreak, CTX-M-15, E. coli, K. pneumoniae</description><subject>Antibiotic resistance</subject><subject>Antibiotics</subject><subject>Bacterial infections</subject><subject>Bacterial pneumonia</subject><subject>Beta lactamases</subject><subject>Cephalosporins</subject><subject>Cluster analysis</subject><subject>ctx-m-15</subject><subject>E coli</subject><subject>Enzymes</subject><subject>Epidemics</subject><subject>Escherichia coli</subject><subject>extended spectrum beta lactamases</subject><subject>Gel electrophoresis</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genotyping</subject><subject>Imipenem</subject><subject>Infants (Newborn)</subject><subject>Infections</subject><subject>Intensive care</subject><subject>k. pneumoniae</subject><subject>Medical personnel</subject><subject>Neonatal intensive care</subject><subject>Neonates</subject><subject>nicu outbreak</subject><subject>Original Research</subject><subject>Outbreaks</subject><subject>Pneumonia</subject><issn>1178-6973</issn><issn>1178-6973</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkt1qFDEUgAdRbKm98gUCggi6NZOfycyNUNZqF1srtgXvwpnMmd3U2WRNMoXe-Rr6eD6J2W7RrphcJCf5zhdyOEXxtKQHrBTq9ezt54NzXiqqmgfFblmqelI1ij-8t98p9mO8onnwphKKPS52uOCsqiTbLX5OL75MTielJJ98tMleIzmKZoHBmoUFYvxgCbiOfBiwjRaHAcjK4bj0zgKSszG1AeErsY6kBZKP6B0kGMjMJXRxbZtCQHLpbCK-J0BOIWHI0Q059nFl12zOPYZf33_Y4RU5h7Gz5DBAa-FJ8aiHIeL-3bpXXL47upgeT07O3s-mhycTIyVNk0oIw1BhXWJLS2kkrZpG9LQGCq2oBeawrvNv-16ymgE3tFKNocb0jYQO-F4x23g7D1d6FewSwo32YPXtgQ9zDSFZM6BuO5MVsjEKpGiVqSVw1QqAliOnHcuuNxvXamyX2Bl0KcCwJd2-cXah5_5a17yslKyy4MWdIPhvI8aklzaadd0d-jFqJqVijFFBM_rsH_TKj8HlUt1SJWO8EX-pOeQPWNf7_K5ZS_VhpVglaspUpg7-Q-XZ4dIa77C3-Xwr4fm9hAXCkBbRD2Oy3sVt8OUGNMHHGLD_U4yS6nUL69zC-q6F-W9XgeBf</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Almogbel, Mohammed</creator><creator>Altheban, Ahmed</creator><creator>Alenezi, Mohammed</creator><creator>Motair, Khalid Al</creator><creator>Menezes, Godfred A</creator><creator>Elabbasy, Mohammed</creator><creator>Hammam, Sahar</creator><creator>Hays, John P</creator><creator>Khan, Mushtaq A</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><general>Dove</general><general>Dove Medical Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9183-4497</orcidid><orcidid>https://orcid.org/0000-0002-2434-1411</orcidid></search><sort><creationdate>20210101</creationdate><title>CTX-M-15 Positive Escherichia coli and Klebsiella pneumoniae Outbreak in the Neonatal Intensive Care Unit of a Maternity Hospital in Ha’il, Saudi Arabia</title><author>Almogbel, Mohammed ; Altheban, Ahmed ; Alenezi, Mohammed ; Motair, Khalid Al ; Menezes, Godfred A ; Elabbasy, Mohammed ; Hammam, Sahar ; Hays, John P ; Khan, Mushtaq A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-644c2e7e81eb015c506994f08a0ab484e69988665ff5282a3c0679c0ccf95ada3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Antibiotic resistance</topic><topic>Antibiotics</topic><topic>Bacterial infections</topic><topic>Bacterial pneumonia</topic><topic>Beta lactamases</topic><topic>Cephalosporins</topic><topic>Cluster analysis</topic><topic>ctx-m-15</topic><topic>E coli</topic><topic>Enzymes</topic><topic>Epidemics</topic><topic>Escherichia coli</topic><topic>extended spectrum beta lactamases</topic><topic>Gel electrophoresis</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genotyping</topic><topic>Imipenem</topic><topic>Infants (Newborn)</topic><topic>Infections</topic><topic>Intensive care</topic><topic>k. pneumoniae</topic><topic>Medical personnel</topic><topic>Neonatal intensive care</topic><topic>Neonates</topic><topic>nicu outbreak</topic><topic>Original Research</topic><topic>Outbreaks</topic><topic>Pneumonia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Almogbel, Mohammed</creatorcontrib><creatorcontrib>Altheban, Ahmed</creatorcontrib><creatorcontrib>Alenezi, Mohammed</creatorcontrib><creatorcontrib>Motair, Khalid Al</creatorcontrib><creatorcontrib>Menezes, Godfred A</creatorcontrib><creatorcontrib>Elabbasy, Mohammed</creatorcontrib><creatorcontrib>Hammam, Sahar</creatorcontrib><creatorcontrib>Hays, John P</creatorcontrib><creatorcontrib>Khan, Mushtaq A</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Infection and drug resistance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Almogbel, Mohammed</au><au>Altheban, Ahmed</au><au>Alenezi, Mohammed</au><au>Motair, Khalid Al</au><au>Menezes, Godfred A</au><au>Elabbasy, Mohammed</au><au>Hammam, Sahar</au><au>Hays, John P</au><au>Khan, Mushtaq A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CTX-M-15 Positive Escherichia coli and Klebsiella pneumoniae Outbreak in the Neonatal Intensive Care Unit of a Maternity Hospital in Ha’il, Saudi Arabia</atitle><jtitle>Infection and drug resistance</jtitle><date>2021-01-01</date><risdate>2021</risdate><volume>14</volume><spage>2843</spage><epage>2849</epage><pages>2843-2849</pages><issn>1178-6973</issn><eissn>1178-6973</eissn><abstract>Objective: The aim of this study was to retrospectively characterize E. coli and K. pneumoniae isolates obtained from neonates during a suspected NICU outbreak of infection in Ha'il, Saudi Arabia during a period of one month (April 2014). Methods: Antibiotic susceptibility patterns, molecular characterization for antibiotic-resistant genes (blaTEM, blaSHV, and blaCTX-M), and genotyping by PFGE and MLST were performed. Results: A total of 24 E. coli and 48 K. pneumoniae isolates were cultured from neonates that had been admitted to the NICU. Among E. coli, the majority of isolates (19/24) were ESBL-positive and all of these nineteen (100%) harbored the CTX-M-15 gene. A total of 15% (3/19) were co-producers of CTX-M-15 and SHV-12, and 68.4% (13/19) were co-producers of CTX-M-15 and TEM-1. Among K. pneumoniae isolates, 87.5% (42/48) were ESBL positive with 92.85% (39/42) of these isolates containing the CTX-M-15 gene. A total of 97% (38/39) of K. pneumoniae were co-producers of CTX-M-15 and SHV-12, and 88% (37/42) were positive for TEM-1. Furthermore, 85.7% (36/42) K. pneumoniae were co-producers of CTX-M-15 and TEM-1. The majority of E. coli isolates (18/19 isolates) were grouped into two genetic clusters by pulsed field gel electrophoresis (PFGE) and all the isolates were found to be ST-131 type. In contrast, K. pneumoniae (31/42) isolates belonged to a single genotypic lineage, and all (100%) isolates belonged to the ST-14 type. Conclusion: This is the first report of CTX-M-15-positive, ESBL E. coli, and K. pneumoniae isolates recovered from an outbreak in an NICU in Ha'il, Saudi Arabia. It is alarming to note the high rate of outbreak isolates with simultaneous production of CTX-M-15 and SHV-12 conferring high-level resistance to oxyimino-cephalosporins. Keywords: extended spectrum [beta]-lactamases, NICU outbreak, CTX-M-15, E. coli, K. pneumoniae</abstract><cop>Macclesfield</cop><pub>Dove Medical Press Limited</pub><pmid>34326652</pmid><doi>10.2147/IDR.S317079</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-9183-4497</orcidid><orcidid>https://orcid.org/0000-0002-2434-1411</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibiotic resistance Antibiotics Bacterial infections Bacterial pneumonia Beta lactamases Cephalosporins Cluster analysis ctx-m-15 E coli Enzymes Epidemics Escherichia coli extended spectrum beta lactamases Gel electrophoresis Genes Genetic aspects Genotyping Imipenem Infants (Newborn) Infections Intensive care k. pneumoniae Medical personnel Neonatal intensive care Neonates nicu outbreak Original Research Outbreaks Pneumonia |
title | CTX-M-15 Positive Escherichia coli and Klebsiella pneumoniae Outbreak in the Neonatal Intensive Care Unit of a Maternity Hospital in Ha’il, Saudi Arabia |
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