Toh Benjamin E W, Paterson David L, Kamolvit Witchuda, Zowawi Hosam, Kvaskoff David, Sidjabat Hanna, Wailan Alexander, Peleg Anton Y, Huber Charlotte A
The University of Queensland, UQ Centre for Clinical Research, Queensland, Royal Brisbane and Women's Hospital Campus, Brisbane, Australia.
The University of Queensland, UQ Centre for Clinical Research, Queensland, Royal Brisbane and Women's Hospital Campus, Brisbane, Australia; King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia; World Health Organization Collaborating Centre for Infection Prevention and Control, and Gulf Cooperation Council Center for Infection Control, Riyadh, Saudi Arabia.
J Microbiol Methods. 2015 Nov;118:128-32. doi: 10.1016/j.mimet.2015.09.006. Epub 2015 Sep 14.
Acinetobacter baumannii, one of the more clinically relevant species in the Acinetobacter genus is well known to be multi-drug resistant and associated with bacteremia, urinary tract infection, pneumonia, wound infection and meningitis. However, it cannot be differentiated from closely related species such as Acinetobacter calcoaceticus, Acinetobacter pittii and Acinetobacter nosocomialis by most phenotypic tests and can only be differentiated by specific, time consuming genotypic tests with very limited use in clinical microbiological laboratories. As a result, these species are grouped into the A. calcoaceticus-A. baumannii (Acb) complex. Herein we investigated the mass spectra of 73 Acinetobacter spp., representing ten different species, using an AB SCIEX 5800 MALDI-TOF MS to differentiate members of the Acinetobacter genus, including the species of the Acb complex. RpoB gene sequencing, 16S rRNA sequencing, and gyrB multiplex PCR were also evaluated as orthogonal methods to identify the organisms used in this study. We found that whilst 16S rRNA and rpoB gene sequencing could not differentiate A. pittii or A. calcoaceticus, they can be differentiated using gyrB multiplex PCR and MALDI-TOF MS. All ten Acinetobacter species investigated could be differentiated by their MALDI-TOF mass spectra.
鲍曼不动杆菌是不动杆菌属中临床相关性较高的物种之一,众所周知它具有多重耐药性,与菌血症、尿路感染、肺炎、伤口感染和脑膜炎有关。然而,通过大多数表型试验,它无法与密切相关的物种如醋酸钙不动杆菌、皮氏不动杆菌和医院不动杆菌区分开来,只能通过特定的、耗时的基因型试验来区分,而这些试验在临床微生物实验室中的应用非常有限。因此,这些物种被归为醋酸钙不动杆菌-鲍曼不动杆菌(Acb)复合体。在此,我们使用AB SCIEX 5800基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)研究了代表十种不同物种的73株不动杆菌属细菌的质谱,以区分不动杆菌属的成员,包括Acb复合体的物种。还评估了rpoB基因测序、16S rRNA测序和gyrB多重PCR作为鉴定本研究中所用生物体的正交方法。我们发现,虽然16S rRNA和rpoB基因测序无法区分皮氏不动杆菌或醋酸钙不动杆菌,但可以使用gyrB多重PCR和MALDI-TOF MS进行区分。所研究的所有十种不动杆菌物种都可以通过它们的MALDI-TOF质谱进行区分。