Carbapenem-Resistant Burkholderia cepacia Complex Isolates Carrying blaNDM−1 and blaNDM−5 in Ventilator-Associated Pneumonia Patients and Contaminated Ventilator Tubing

IF 3.5 2区 农林科学 Q2 INFECTIOUS DISEASES Transboundary and Emerging Diseases Pub Date : 2024-08-30 DOI:10.1155/2024/3352135
Muhammad Saeed, Farhan Rasheed, Muhammad Hidayat Rasool, Sumreen Hayat, Mohsin Khurshid
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Abstract

Ventilator-associated pneumonia (VAP) represents an important nosocomial infection, frequently encountered in intensive care unit (ICU) settings which results in prolonged hospitals stays. The nosocomial infections caused by Burkholderia cepacia complex (BCC) bacteria pose a significant challenge in healthcare settings owing to their intrinsic resistance to many antibiotics. This study investigates the antimicrobial susceptibility patterns and mechanisms of carbapenem resistance among BCC bacteria from VAP patients and the ventilator tubing. The blood and respiratory specimens from patients diagnosed with VAP were collected. In addition, the ventilators were also screened for the presence of BCC bacteria. The susceptibility profiling of BCC isolates was performed against the various antimicrobial agents, and screening for acquired beta-lactamase enzymes was conducted by polymerase chain reaction. Out of the total 134 patients with BCC-associated VAP, B. cepacia, Burkholderia multivorans, and Burkholderia cenocepacia was 68.7% (n = 92), 18.7% (n = 25), and 12.7% (n = 17). Overall, the BCC isolates showed varying susceptibility to different antibiotics: 76.9% were susceptible to chloramphenicol, 76.1% to minocycline, 69.4% to meropenem, 60.4% to ceftazidime, 51.5% to trimethoprim-sulfamethoxazole, and 50% to levofloxacin. Resistance to ceftazidime (51/92, 55.4%) and meropenem (36/92, 39.1%) was exclusively observed in B. cepacia isolates, and all isolates of B. multivorans and B. cenocepacia were found to be susceptible to both beta-lactam drugs. Among the 134 clinical isolates, 15 were found to harbor the blaNDM variants, that is, blaNDM−1 and blaNDM−5. All carbapenem-resistant isolates from the ventilator tubing were identified as B. cepacia and were found to harbor either the blaNDM−1 or the blaNDM−5 variants. The observed increase in resistance and the emergence of acquired beta-lactamases among BCC isolates highlight a concerning trend that could potentially lead to serious outbreaks.

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呼吸机相关肺炎患者和受污染呼吸机管道中携带 blaNDM-1 和 blaNDM-5 的耐碳青霉烯类伯克霍尔德氏菌复合物分离株
呼吸机相关肺炎(VAP)是重症监护室(ICU)环境中经常遇到的一种重要的院内感染,会导致患者住院时间延长。由于伯克霍尔德氏菌复合体(BCC)细菌对多种抗生素具有固有耐药性,因此其引起的院内感染给医疗机构带来了巨大挑战。本研究调查了 VAP 患者和呼吸机管道中 BCC 细菌的抗菌药敏感性模式和碳青霉烯耐药机制。研究收集了确诊为 VAP 患者的血液和呼吸道标本。此外,还筛查了呼吸机中是否存在 BCC 细菌。对 BCC 分离菌进行了各种抗菌药物敏感性分析,并通过聚合酶链式反应对获得性β-内酰胺酶进行了筛查。在134名BCC相关VAP患者中,头孢杆菌、多房伯克霍尔德氏菌和塞那帕克伯克霍尔德氏菌分别占68.7%(92人)、18.7%(25人)和12.7%(17人)。总体而言,BCC 分离物对不同抗生素的敏感性各不相同:76.9%对氯霉素敏感,76.1%对米诺环素敏感,69.4%对美罗培南敏感,60.4%对头孢他啶敏感,51.5%对三甲双胍-磺胺甲噁唑敏感,50%对左氧氟沙星敏感。对头孢他啶(51/92,55.4%)和美罗培南(36/92,39.1%)产生抗药性的只有头孢杆菌分离株,而多杀性头孢杆菌和肠杆菌的所有分离株都对这两种β-内酰胺类药物敏感。在 134 个临床分离株中,发现 15 个携带 blaNDM 变异株,即 blaNDM-1 和 blaNDM-5。从呼吸机管道中分离出的所有碳青霉烯耐药菌株均被鉴定为B. cepacia,并发现它们携带 blaNDM-1 或 blaNDM-5 变体。在 BCC 分离物中观察到的耐药性增加和获得性β-内酰胺酶的出现凸显了一种令人担忧的趋势,这种趋势有可能导致严重的疫情爆发。
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来源期刊
Transboundary and Emerging Diseases
Transboundary and Emerging Diseases 农林科学-传染病学
CiteScore
8.90
自引率
9.30%
发文量
350
审稿时长
1 months
期刊介绍: Transboundary and Emerging Diseases brings together in one place the latest research on infectious diseases considered to hold the greatest economic threat to animals and humans worldwide. The journal provides a venue for global research on their diagnosis, prevention and management, and for papers on public health, pathogenesis, epidemiology, statistical modeling, diagnostics, biosecurity issues, genomics, vaccine development and rapid communication of new outbreaks. Papers should include timely research approaches using state-of-the-art technologies. The editors encourage papers adopting a science-based approach on socio-economic and environmental factors influencing the management of the bio-security threat posed by these diseases, including risk analysis and disease spread modeling. Preference will be given to communications focusing on novel science-based approaches to controlling transboundary and emerging diseases. The following topics are generally considered out-of-scope, but decisions are made on a case-by-case basis (for example, studies on cryptic wildlife populations, and those on potential species extinctions): Pathogen discovery: a common pathogen newly recognised in a specific country, or a new pathogen or genetic sequence for which there is little context about — or insights regarding — its emergence or spread. Prevalence estimation surveys and risk factor studies based on survey (rather than longitudinal) methodology, except when such studies are unique. Surveys of knowledge, attitudes and practices are within scope. Diagnostic test development if not accompanied by robust sensitivity and specificity estimation from field studies. Studies focused only on laboratory methods in which relevance to disease emergence and spread is not obvious or can not be inferred (“pure research” type studies). Narrative literature reviews which do not generate new knowledge. Systematic and scoping reviews, and meta-analyses are within scope.
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