Raquel Zaragozá González, Laura Iglesias Llorente, Estefanía Águila Fernández-Paniagua, Laura Alonso Acero, Teresa Monserrat Blázquez, Iballa Horcajada, Laura Florén Florén Zabala
{"title":"感染产亚胺培南酶-1 鲁德韦希氏肠杆菌的医院内患者群。","authors":"Raquel Zaragozá González, Laura Iglesias Llorente, Estefanía Águila Fernández-Paniagua, Laura Alonso Acero, Teresa Monserrat Blázquez, Iballa Horcajada, Laura Florén Florén Zabala","doi":"10.1099/jmm.0.001919","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction.</b> Imipenemase (IMI) enzymes are an uncommon class A carbapenemases that have been isolated from aquatic environments and, occasionally, from clinical isolates of <i>Enterobacterales</i>.<b>Aim.</b> We describe a cluster of three patients infected by IMI-1 carbapenemase-producing <i>Enterobacter ludwigii</i> (IMI-1-Elud) in a tertiary university hospital in Gran Canaria, Spain.<b>Methodology.</b> Antimicrobial susceptibility was determined using the Vitek2 AST-N355 card and antibiotic gradient strips. The modified carbapenem inactivation method (CIM) test was performed in cases where the ertapenem MIC value was higher than 0.125 mg l<sup>-1</sup>. The carbapenemase was identified by PCR and DNA microarray and later characterized by whole-genome next-generation sequencing (NGS) with Illumina.<b>Results.</b> Three patients presented thoracic or abdominal infections caused by IMI-1-Elud ST1677 from 14 June 2022 to 14 July 2022. All patients underwent at least one gastroscopy during their admission, and two of them were located in adjoining rooms. Isolates were resistant to carbapenems, colistin and fosfomycin but susceptible to ciprofloxacin. IMI/NMC-A carbapenemase was detected by PCR and hybridization test and confirmed by NGS as IMI-1. All patients underwent at least one gastroscopy, and two of them were in nearby rooms. Patients showed microbiological and clinical improvement following focus drainage and targeted antibiotic treatment with a fluoroquinolone.<b>Conclusions.</b> This study reports the first documented global outbreak of patients infected with IMI-1-Elud. The source appeared to be related to endoscopes. Contact transmission may also have played a role. A screening method such as the modified CIM test is crucial for detecting less common carbapenemases that might not be identified by rapid molecular or immunochromatographic tests, as these often do not include <i>bla</i> <sub>IMI</sub> genes, which could lead to the undetected dissemination of carbapenemase-producing Enterobacterales. Effective infection source control and targeted treatment are essential for achieving a favourable clinical outcome.</p>","PeriodicalId":94093,"journal":{"name":"Journal of medical microbiology","volume":"73 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Nosocomial cluster of patients infected with imipenemase-1-producing <i>Enterobacter ludwigii</i>.\",\"authors\":\"Raquel Zaragozá González, Laura Iglesias Llorente, Estefanía Águila Fernández-Paniagua, Laura Alonso Acero, Teresa Monserrat Blázquez, Iballa Horcajada, Laura Florén Florén Zabala\",\"doi\":\"10.1099/jmm.0.001919\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction.</b> Imipenemase (IMI) enzymes are an uncommon class A carbapenemases that have been isolated from aquatic environments and, occasionally, from clinical isolates of <i>Enterobacterales</i>.<b>Aim.</b> We describe a cluster of three patients infected by IMI-1 carbapenemase-producing <i>Enterobacter ludwigii</i> (IMI-1-Elud) in a tertiary university hospital in Gran Canaria, Spain.<b>Methodology.</b> Antimicrobial susceptibility was determined using the Vitek2 AST-N355 card and antibiotic gradient strips. The modified carbapenem inactivation method (CIM) test was performed in cases where the ertapenem MIC value was higher than 0.125 mg l<sup>-1</sup>. The carbapenemase was identified by PCR and DNA microarray and later characterized by whole-genome next-generation sequencing (NGS) with Illumina.<b>Results.</b> Three patients presented thoracic or abdominal infections caused by IMI-1-Elud ST1677 from 14 June 2022 to 14 July 2022. All patients underwent at least one gastroscopy during their admission, and two of them were located in adjoining rooms. Isolates were resistant to carbapenems, colistin and fosfomycin but susceptible to ciprofloxacin. IMI/NMC-A carbapenemase was detected by PCR and hybridization test and confirmed by NGS as IMI-1. All patients underwent at least one gastroscopy, and two of them were in nearby rooms. Patients showed microbiological and clinical improvement following focus drainage and targeted antibiotic treatment with a fluoroquinolone.<b>Conclusions.</b> This study reports the first documented global outbreak of patients infected with IMI-1-Elud. The source appeared to be related to endoscopes. Contact transmission may also have played a role. A screening method such as the modified CIM test is crucial for detecting less common carbapenemases that might not be identified by rapid molecular or immunochromatographic tests, as these often do not include <i>bla</i> <sub>IMI</sub> genes, which could lead to the undetected dissemination of carbapenemase-producing Enterobacterales. 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引用次数: 0
摘要
简介。亚胺培南酶(IMI)是一种不常见的 A 类碳青霉烯酶,从水生环境中分离出来,偶尔也从临床分离的肠杆菌中分离出来。我们描述了西班牙大加那利岛一所三级大学医院中三名感染产 IMI-1 型碳青霉烯酶的路德维希肠杆菌(IMI-1-Elud)的患者。使用 Vitek2 AST-N355 卡和抗生素梯度条测定抗菌药敏感性。如果厄他培南的 MIC 值高于 0.125 毫克/升,则进行改良碳青霉烯灭活法(CIM)测试。通过 PCR 和 DNA 微阵列鉴定碳青霉烯酶,随后使用 Illumina 进行全基因组下一代测序(NGS)。2022年6月14日至2022年7月14日期间,3名患者出现了由IMI-1-Elud ST1677引起的胸部或腹部感染。所有患者在入院期间至少接受了一次胃镜检查,其中两名患者的病房相邻。分离菌株对碳青霉烯类、可乐定和磷霉素耐药,但对环丙沙星敏感。通过 PCR 和杂交试验检测到 IMI/NMC-A 碳青霉烯酶,并通过 NGS 确认为 IMI-1。所有患者都接受了至少一次胃镜检查,其中两名患者的病房就在附近。在病灶引流和使用氟喹诺酮类药物进行针对性抗生素治疗后,患者的微生物学和临床症状均有所改善。本研究报告了首次记录在案的全球 IMI-1-Elud 感染爆发。病源似乎与内窥镜有关。接触传播也可能是其中一个原因。改良 CIM 检验等筛查方法对于检测快速分子检验或免疫层析检验可能无法识别的较少见的碳青霉烯酶至关重要,因为这些检验通常不包括 bla IMI 基因,这可能导致产生碳青霉烯酶的肠杆菌传播而不被发现。有效的感染源控制和针对性治疗对于取得良好的临床效果至关重要。
Nosocomial cluster of patients infected with imipenemase-1-producing Enterobacter ludwigii.
Introduction. Imipenemase (IMI) enzymes are an uncommon class A carbapenemases that have been isolated from aquatic environments and, occasionally, from clinical isolates of Enterobacterales.Aim. We describe a cluster of three patients infected by IMI-1 carbapenemase-producing Enterobacter ludwigii (IMI-1-Elud) in a tertiary university hospital in Gran Canaria, Spain.Methodology. Antimicrobial susceptibility was determined using the Vitek2 AST-N355 card and antibiotic gradient strips. The modified carbapenem inactivation method (CIM) test was performed in cases where the ertapenem MIC value was higher than 0.125 mg l-1. The carbapenemase was identified by PCR and DNA microarray and later characterized by whole-genome next-generation sequencing (NGS) with Illumina.Results. Three patients presented thoracic or abdominal infections caused by IMI-1-Elud ST1677 from 14 June 2022 to 14 July 2022. All patients underwent at least one gastroscopy during their admission, and two of them were located in adjoining rooms. Isolates were resistant to carbapenems, colistin and fosfomycin but susceptible to ciprofloxacin. IMI/NMC-A carbapenemase was detected by PCR and hybridization test and confirmed by NGS as IMI-1. All patients underwent at least one gastroscopy, and two of them were in nearby rooms. Patients showed microbiological and clinical improvement following focus drainage and targeted antibiotic treatment with a fluoroquinolone.Conclusions. This study reports the first documented global outbreak of patients infected with IMI-1-Elud. The source appeared to be related to endoscopes. Contact transmission may also have played a role. A screening method such as the modified CIM test is crucial for detecting less common carbapenemases that might not be identified by rapid molecular or immunochromatographic tests, as these often do not include blaIMI genes, which could lead to the undetected dissemination of carbapenemase-producing Enterobacterales. Effective infection source control and targeted treatment are essential for achieving a favourable clinical outcome.