Hans Kollenda, Hagen Frickmann, Rania Ben Helal, Dorothea Franziska Wiemer, Habiba Naija, Mohamed Sélim El Asli, Melanie Egold, Joachim Jakob Bugert, Susann Handrick, Roman Wölfel, Farouk Barguellil, Mohamed Ben Moussa
{"title":"2014年至2018年在突尼斯一家医院收集的耐厄他培烯肠杆菌科细菌中碳青霉烯酶的筛查","authors":"Hans Kollenda, Hagen Frickmann, Rania Ben Helal, Dorothea Franziska Wiemer, Habiba Naija, Mohamed Sélim El Asli, Melanie Egold, Joachim Jakob Bugert, Susann Handrick, Roman Wölfel, Farouk Barguellil, Mohamed Ben Moussa","doi":"10.1556/1886.2018.00033","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Carbapenem-resistance is frequently detected in <i>Enterobacteriaceae</i> isolated from patients in Tunisia. The study was performed to identify frequent carbapenemases in Tunisian isolates.</p><p><strong>Methods: </strong>Between May 2014 and January 2018, 197 ertapenem-resistant <i>Enterobacteriaceae</i> were isolated at the microbiological department of the Military Hospital of Tunis. The strains were phenotypically characterized and then subjected to in-house polymerase chain reaction (PCR) targeting the carbapenemase genes <i>bla<sub>IMP</sub>, bla<sub>VIM</sub>, bla<sub>NDM</sub>, bla<sub>SPM</sub>, bla<sub>AIM</sub>, bla<sub>DIM</sub>,bla<sub>GIM</sub>, bla<sub>SIM</sub>, bla<sub>KPC</sub>, bla<sub>BIC</sub></i> , and <i>bla<sub>OXA-48</sub>.</i></p><p><strong>Results: </strong>The assessed 197 ertapenem-resistant <i>Enterobacteriaceae</i> from Tunis comprised 170 <i>Klebsiella pneumoniae</i>, <i>19 Enterobacter cloacae</i>, 6 <i>Escherichia coli</i>, <i>1 Citrobacter sedlakii</i>, and 1 <i>Enterobacter asburiae.</i> Thereby, 55 out of 197 isolates (27.9%) were from blood cultures, suggesting a systemic disease. The carbapenemase gene <i>bla<sub>OXA-48</sub></i> quantitatively dominated by far with 153 detections, followed by <i>bla<sub>NDM</sub></i> with 14 detections, which were distributed about the whole study interval. In contrast, <i>bla<sub>BIC</sub></i> and <i>bla<sub>VIM</sub></i> were only infrequently identified in 5 and 3 cases, respectively, while the other carbapenamases were not observed.</p><p><strong>Conclusions: </strong>The carbapenemase gene <i>bla<sub>OXA-48</sub></i> was identified in the vast majority of ertapenem-resistant Tunisian <i>Enterobacteriaceae</i> while all other assessed carbapenemases were much less abundant. In a quantitatively relevant minority of isolates, the applied PCR-based screening approach did not identify any carbapenemases.</p>","PeriodicalId":11929,"journal":{"name":"European Journal of Microbiology & Immunology","volume":"9 1","pages":"9-13"},"PeriodicalIF":0.0000,"publicationDate":"2019-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1556/1886.2018.00033","citationCount":"19","resultStr":"{\"title\":\"Screening for Carbapenemases in Ertapenem-Resistant <i>Enterobacteriaceae</i> Collected at a Tunisian Hospital Between 2014 and 2018.\",\"authors\":\"Hans Kollenda, Hagen Frickmann, Rania Ben Helal, Dorothea Franziska Wiemer, Habiba Naija, Mohamed Sélim El Asli, Melanie Egold, Joachim Jakob Bugert, Susann Handrick, Roman Wölfel, Farouk Barguellil, Mohamed Ben Moussa\",\"doi\":\"10.1556/1886.2018.00033\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Carbapenem-resistance is frequently detected in <i>Enterobacteriaceae</i> isolated from patients in Tunisia. The study was performed to identify frequent carbapenemases in Tunisian isolates.</p><p><strong>Methods: </strong>Between May 2014 and January 2018, 197 ertapenem-resistant <i>Enterobacteriaceae</i> were isolated at the microbiological department of the Military Hospital of Tunis. The strains were phenotypically characterized and then subjected to in-house polymerase chain reaction (PCR) targeting the carbapenemase genes <i>bla<sub>IMP</sub>, bla<sub>VIM</sub>, bla<sub>NDM</sub>, bla<sub>SPM</sub>, bla<sub>AIM</sub>, bla<sub>DIM</sub>,bla<sub>GIM</sub>, bla<sub>SIM</sub>, bla<sub>KPC</sub>, bla<sub>BIC</sub></i> , and <i>bla<sub>OXA-48</sub>.</i></p><p><strong>Results: </strong>The assessed 197 ertapenem-resistant <i>Enterobacteriaceae</i> from Tunis comprised 170 <i>Klebsiella pneumoniae</i>, <i>19 Enterobacter cloacae</i>, 6 <i>Escherichia coli</i>, <i>1 Citrobacter sedlakii</i>, and 1 <i>Enterobacter asburiae.</i> Thereby, 55 out of 197 isolates (27.9%) were from blood cultures, suggesting a systemic disease. The carbapenemase gene <i>bla<sub>OXA-48</sub></i> quantitatively dominated by far with 153 detections, followed by <i>bla<sub>NDM</sub></i> with 14 detections, which were distributed about the whole study interval. In contrast, <i>bla<sub>BIC</sub></i> and <i>bla<sub>VIM</sub></i> were only infrequently identified in 5 and 3 cases, respectively, while the other carbapenamases were not observed.</p><p><strong>Conclusions: </strong>The carbapenemase gene <i>bla<sub>OXA-48</sub></i> was identified in the vast majority of ertapenem-resistant Tunisian <i>Enterobacteriaceae</i> while all other assessed carbapenemases were much less abundant. In a quantitatively relevant minority of isolates, the applied PCR-based screening approach did not identify any carbapenemases.</p>\",\"PeriodicalId\":11929,\"journal\":{\"name\":\"European Journal of Microbiology & Immunology\",\"volume\":\"9 1\",\"pages\":\"9-13\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-02-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1556/1886.2018.00033\",\"citationCount\":\"19\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Microbiology & Immunology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1556/1886.2018.00033\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/3/18 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Microbiology & Immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1556/1886.2018.00033","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/3/18 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
Screening for Carbapenemases in Ertapenem-Resistant Enterobacteriaceae Collected at a Tunisian Hospital Between 2014 and 2018.
Background: Carbapenem-resistance is frequently detected in Enterobacteriaceae isolated from patients in Tunisia. The study was performed to identify frequent carbapenemases in Tunisian isolates.
Methods: Between May 2014 and January 2018, 197 ertapenem-resistant Enterobacteriaceae were isolated at the microbiological department of the Military Hospital of Tunis. The strains were phenotypically characterized and then subjected to in-house polymerase chain reaction (PCR) targeting the carbapenemase genes blaIMP, blaVIM, blaNDM, blaSPM, blaAIM, blaDIM,blaGIM, blaSIM, blaKPC, blaBIC , and blaOXA-48.
Results: The assessed 197 ertapenem-resistant Enterobacteriaceae from Tunis comprised 170 Klebsiella pneumoniae, 19 Enterobacter cloacae, 6 Escherichia coli, 1 Citrobacter sedlakii, and 1 Enterobacter asburiae. Thereby, 55 out of 197 isolates (27.9%) were from blood cultures, suggesting a systemic disease. The carbapenemase gene blaOXA-48 quantitatively dominated by far with 153 detections, followed by blaNDM with 14 detections, which were distributed about the whole study interval. In contrast, blaBIC and blaVIM were only infrequently identified in 5 and 3 cases, respectively, while the other carbapenamases were not observed.
Conclusions: The carbapenemase gene blaOXA-48 was identified in the vast majority of ertapenem-resistant Tunisian Enterobacteriaceae while all other assessed carbapenemases were much less abundant. In a quantitatively relevant minority of isolates, the applied PCR-based screening approach did not identify any carbapenemases.