Hadeel Elzeny, Wegdan Mohamed, Enas Daef, Omnia El-Badawy, Lamiaa Shaaban, Naglaa S Osman, Safy Hadiya, Sherine Aly
{"title":"埃及呼吸机相关肺炎患者中多重广泛耐药高毒肺炎克雷伯菌克隆的检测","authors":"Hadeel Elzeny, Wegdan Mohamed, Enas Daef, Omnia El-Badawy, Lamiaa Shaaban, Naglaa S Osman, Safy Hadiya, Sherine Aly","doi":"10.1099/jmm.0.001701","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction.</b> Hypervirulent-<i>K. pneumoniae</i> (hvKP) is an evolving pathotype that is more virulent than the classical-<i>K. pneumoniae</i> (cKP) and causes serious fatal illnesses.<b>Hypothesis/Gap Statement.</b> Although there are few reports on hvKP isolated from Egyptian patients, the molecular characteristics and clonal relatedness of MDR-hvKP have not been adequately investigated.<b>Aim.</b> To investigate the microbiological and genetic characteristics as well as the epidemiology of hvKP induced ventilator-associated pneumonia (VAP).<b>Methodology.</b> A retrospective study of 59 <i>K</i>. <i>pneumoniae</i> inducing VAP was conducted at Assiut University Hospitals from November 2017 to January 2019. All <i>K. pneumoniae</i> were tested for resistance phenotype, capsular genotype (K1 and K2), virulence gene profile (<i>c-rmpA, p-rmpA, iucA, kfu, iroB, iroN</i>), and the presence of resistance genes (<i>blaNDM-1, blaCTX-M-3-</i>like<i>, blaCTX-M-14-</i>like). Clonal relatedness was assessed by Pulsed field gel electrophoresis (PFGE).<b>Result.</b> HvKP accounted for 89.8 % (53/59) of <i>K. pneumoniae</i> isolates with ~95 % exhibiting extensively-drug resistant (XDR) phenotype. Hypermucoviscous phenotype was detected in 19 (35.8 %) hvKP and K2 capsular gene was identified in 18 (33.9 %) of hvKP. Regarding the virulence genotype of hvKP strains, <i>iucA</i> was the most prevalent virulence gene (98.1%), while p<i>-rmpA</i> and <i>kfu</i> were detected in 75.4 and 52.8 % of hvKP strains, respectively. Resistance genes were highly prevalent in both cKP and hvKP with <i>blaCTX-M-3-like</i> being more prevalent in hvKP (100 % vs 94.3 % for <i>blaNDM-1,</i> 50 % vs 62.2 % for <i>blaCTX-M-3-</i>like and 83.3 % vs 69.8 % for <i>blaCTX-M-14</i> <sub>-</sub>like, respectively). PFGE typing of 29 representative <i>K. pneumoniae</i> revealed 15 pulsotypes, with identical hvKP pulsotypes isolated from different ICUs at different times and several hvKP and cKP isolates belonged to the same pulsotype.<b>Conclusion.</b> This study highlights the dominance and clonal spread of XDR-hvKP strains at Assiut University Hospital in Egypt. Physicians should be aware of the increased risk of hvKP induced-VAP and support further epidemiologic studies.</p>","PeriodicalId":16343,"journal":{"name":"Journal of medical microbiology","volume":"72 6","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Detection of multiple extensively-drug resistant hypervirulent <i>Klebsiella pneumoniae</i> clones from patients with ventilator-associated pneumonia in Egypt.\",\"authors\":\"Hadeel Elzeny, Wegdan Mohamed, Enas Daef, Omnia El-Badawy, Lamiaa Shaaban, Naglaa S Osman, Safy Hadiya, Sherine Aly\",\"doi\":\"10.1099/jmm.0.001701\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction.</b> Hypervirulent-<i>K. pneumoniae</i> (hvKP) is an evolving pathotype that is more virulent than the classical-<i>K. pneumoniae</i> (cKP) and causes serious fatal illnesses.<b>Hypothesis/Gap Statement.</b> Although there are few reports on hvKP isolated from Egyptian patients, the molecular characteristics and clonal relatedness of MDR-hvKP have not been adequately investigated.<b>Aim.</b> To investigate the microbiological and genetic characteristics as well as the epidemiology of hvKP induced ventilator-associated pneumonia (VAP).<b>Methodology.</b> A retrospective study of 59 <i>K</i>. <i>pneumoniae</i> inducing VAP was conducted at Assiut University Hospitals from November 2017 to January 2019. All <i>K. pneumoniae</i> were tested for resistance phenotype, capsular genotype (K1 and K2), virulence gene profile (<i>c-rmpA, p-rmpA, iucA, kfu, iroB, iroN</i>), and the presence of resistance genes (<i>blaNDM-1, blaCTX-M-3-</i>like<i>, blaCTX-M-14-</i>like). Clonal relatedness was assessed by Pulsed field gel electrophoresis (PFGE).<b>Result.</b> HvKP accounted for 89.8 % (53/59) of <i>K. pneumoniae</i> isolates with ~95 % exhibiting extensively-drug resistant (XDR) phenotype. Hypermucoviscous phenotype was detected in 19 (35.8 %) hvKP and K2 capsular gene was identified in 18 (33.9 %) of hvKP. Regarding the virulence genotype of hvKP strains, <i>iucA</i> was the most prevalent virulence gene (98.1%), while p<i>-rmpA</i> and <i>kfu</i> were detected in 75.4 and 52.8 % of hvKP strains, respectively. Resistance genes were highly prevalent in both cKP and hvKP with <i>blaCTX-M-3-like</i> being more prevalent in hvKP (100 % vs 94.3 % for <i>blaNDM-1,</i> 50 % vs 62.2 % for <i>blaCTX-M-3-</i>like and 83.3 % vs 69.8 % for <i>blaCTX-M-14</i> <sub>-</sub>like, respectively). PFGE typing of 29 representative <i>K. pneumoniae</i> revealed 15 pulsotypes, with identical hvKP pulsotypes isolated from different ICUs at different times and several hvKP and cKP isolates belonged to the same pulsotype.<b>Conclusion.</b> This study highlights the dominance and clonal spread of XDR-hvKP strains at Assiut University Hospital in Egypt. Physicians should be aware of the increased risk of hvKP induced-VAP and support further epidemiologic studies.</p>\",\"PeriodicalId\":16343,\"journal\":{\"name\":\"Journal of medical microbiology\",\"volume\":\"72 6\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of medical microbiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1099/jmm.0.001701\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medical microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1099/jmm.0.001701","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 1
摘要
介绍。Hypervirulent-K。肺炎(hvKP)是一种不断进化的病型,其毒性比经典的k型肺炎更强。肺炎(cKP)并引起严重的致命疾病。假设/差距语句。虽然从埃及患者中分离hvKP的报道很少,但对耐多药hvKP的分子特征和克隆相关性尚未进行充分的研究。目的探讨hvKP致呼吸机相关性肺炎(VAP)的微生物学、遗传学特征及流行病学特点。对2017年11月至2019年1月阿西尤特大学附属医院59例肺炎克雷伯菌诱导的VAP进行回顾性研究。检测所有肺炎克雷伯菌的耐药表型、荚膜基因型(K1和K2)、毒力基因谱(c-rmpA、p-rmpA、iucA、kfu、iroB、iroN)以及耐药基因(blaNDM-1、blactx - m -3样、blactx - m -14样)的存在。通过脉冲场凝胶电泳(PFGE)检测克隆亲缘性。HvKP占肺炎克雷伯菌分离株的89.8%(53/59),其中~ 95%表现出广泛耐药表型。19例(35.8%)hvKP检测到高粘滞表型,18例(33.9%)hvKP检测到K2荚膜基因。从毒力基因型来看,iucA基因最多(98.1%),p-rmpA和kfu基因分别占75.4和52.8%。耐药基因在cKP和hvKP中都非常普遍,其中blactx - m -3样在hvKP中更为普遍(blaNDM-1为100%比94.3%,blactx - m -3样为50%比62.2%,blaCTX-M-14样为83.3%比69.8%)。29例典型肺炎克雷伯菌PFGE分型显示15种脉冲型,不同icu不同时间分离的hvKP脉冲型相同,hvKP和cKP分离株属于同一脉冲型。这项研究强调了埃及Assiut大学医院XDR-hvKP菌株的优势和克隆传播。医生应该意识到hvKP诱发vap的风险增加,并支持进一步的流行病学研究。
Detection of multiple extensively-drug resistant hypervirulent Klebsiella pneumoniae clones from patients with ventilator-associated pneumonia in Egypt.
Introduction. Hypervirulent-K. pneumoniae (hvKP) is an evolving pathotype that is more virulent than the classical-K. pneumoniae (cKP) and causes serious fatal illnesses.Hypothesis/Gap Statement. Although there are few reports on hvKP isolated from Egyptian patients, the molecular characteristics and clonal relatedness of MDR-hvKP have not been adequately investigated.Aim. To investigate the microbiological and genetic characteristics as well as the epidemiology of hvKP induced ventilator-associated pneumonia (VAP).Methodology. A retrospective study of 59 K. pneumoniae inducing VAP was conducted at Assiut University Hospitals from November 2017 to January 2019. All K. pneumoniae were tested for resistance phenotype, capsular genotype (K1 and K2), virulence gene profile (c-rmpA, p-rmpA, iucA, kfu, iroB, iroN), and the presence of resistance genes (blaNDM-1, blaCTX-M-3-like, blaCTX-M-14-like). Clonal relatedness was assessed by Pulsed field gel electrophoresis (PFGE).Result. HvKP accounted for 89.8 % (53/59) of K. pneumoniae isolates with ~95 % exhibiting extensively-drug resistant (XDR) phenotype. Hypermucoviscous phenotype was detected in 19 (35.8 %) hvKP and K2 capsular gene was identified in 18 (33.9 %) of hvKP. Regarding the virulence genotype of hvKP strains, iucA was the most prevalent virulence gene (98.1%), while p-rmpA and kfu were detected in 75.4 and 52.8 % of hvKP strains, respectively. Resistance genes were highly prevalent in both cKP and hvKP with blaCTX-M-3-like being more prevalent in hvKP (100 % vs 94.3 % for blaNDM-1, 50 % vs 62.2 % for blaCTX-M-3-like and 83.3 % vs 69.8 % for blaCTX-M-14-like, respectively). PFGE typing of 29 representative K. pneumoniae revealed 15 pulsotypes, with identical hvKP pulsotypes isolated from different ICUs at different times and several hvKP and cKP isolates belonged to the same pulsotype.Conclusion. This study highlights the dominance and clonal spread of XDR-hvKP strains at Assiut University Hospital in Egypt. Physicians should be aware of the increased risk of hvKP induced-VAP and support further epidemiologic studies.
期刊介绍:
Journal of Medical Microbiology provides comprehensive coverage of medical, dental and veterinary microbiology, and infectious diseases. We welcome everything from laboratory research to clinical trials, including bacteriology, virology, mycology and parasitology. We publish articles under the following subject categories: Antimicrobial resistance; Clinical microbiology; Disease, diagnosis and diagnostics; Medical mycology; Molecular and microbial epidemiology; Microbiome and microbial ecology in health; One Health; Pathogenesis, virulence and host response; Prevention, therapy and therapeutics