McCracken M, DeCorby M, Fuller J, Loo V, Hoban D J, Zhanel G G, Mulvey M R
National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, Manitoba, Canada.
J Antimicrob Chemother. 2009 Sep;64(3):552-5. doi: 10.1093/jac/dkp225. Epub 2009 Jul 3.
Multidrug-resistant (MDR) Acinetobacter baumannii is a growing concern in many countries. This report describes patient demographics, antimicrobial susceptibilities and molecular characteristics of A. baumannii cases identified through the Canadian Ward Surveillance Study (CANWARD). In addition, clinical cases involving MDR carbapenem-resistant A. baumannii are also detailed in this report.
From January to December 2007, 12 hospital centres across Canada submitted pathogens from clinics, emergency rooms, intensive care units and medical/surgical wards as part of the CANWARD study. MICs were determined using microbroth dilution (CLSI). PCR and sequence analysis identified OXA genes among carbapenem-resistant isolates. PFGE was used to determine genetic relatedness and compare representatives of the Midlands 2 strain, OXA-23 clone 1 or 2, T strains and isolates collected from military sources.
This study identified A. baumannii in 0.33% (n = 26) of infections. The majority of isolates remained susceptible to the antimicrobials tested, however, 7.7% (n = 2) displayed an MDR phenotype, including resistance to carbapenems. In one isolate bla(OXA-58) was found to be the likely cause of carbapenem resistance while the other isolate had an insertion sequence element upstream of its intrinsic bla(OXA-51). The clinical data of these two isolates suggest that one is travel-related while the source of the other remains unknown.
A. baumannii infections from Canadian hospitals were relatively low. Carbapenem-resistant MDR A. baumannii were also rare and unrelated to previously observed isolates from military sources. Continued surveillance in Canada is suggested in order to determine if such organisms will become a problem.
多重耐药鲍曼不动杆菌在许多国家日益引起关注。本报告描述了通过加拿大病房监测研究(CANWARD)确定的鲍曼不动杆菌病例的患者人口统计学特征、抗菌药物敏感性及分子特征。此外,本报告还详细介绍了涉及多重耐药碳青霉烯类耐药鲍曼不动杆菌的临床病例。
2007年1月至12月,作为CANWARD研究的一部分,加拿大12家医院中心提交了来自诊所、急诊室、重症监护病房及内科/外科病房的病原体。采用微量肉汤稀释法(CLSI)测定最低抑菌浓度(MIC)。通过聚合酶链反应(PCR)和序列分析鉴定碳青霉烯类耐药菌株中的OXA基因。采用脉冲场凝胶电泳(PFGE)确定遗传相关性,并比较米德兰兹2菌株、OXA-23克隆1或2、T菌株以及从军事来源收集的分离株的代表菌株。
本研究在0.33%(n = 26)的感染病例中鉴定出鲍曼不动杆菌。大多数分离株对所测试的抗菌药物仍敏感,然而,7.7%(n = 2)表现出多重耐药表型,包括对碳青霉烯类耐药。在一株分离株中,bla(OXA-58)被发现可能是碳青霉烯类耐药的原因,而另一株分离株在其固有bla(OXA-51)上游有一个插入序列元件。这两株分离株的临床数据表明,一株与旅行有关,而另一株的来源仍不明。
加拿大医院的鲍曼不动杆菌感染率相对较低。碳青霉烯类耐药多重耐药鲍曼不动杆菌也很罕见,且与先前从军事来源观察到的分离株无关。建议在加拿大继续进行监测,以确定此类微生物是否会成为一个问题。