Hamouda Ahmed
Department of Molecular and Clinical Biochemistry, College of Medicine, University of Taibah, University Road, PO Box 344, Medinah, Kingdom of Saudi Arabia.
Curr Microbiol. 2017 Sep;74(9):1118-1122. doi: 10.1007/s00284-017-1283-1. Epub 2017 Jun 29.
Acinetobacter baumannii is a notorious nosocomial pathogen known for its ability to cause severe infections, especially in intensive care units. The identification of a conserved gene encoding a hypothetical protein in A. baumannii isolates but not in other Acinetobacter species during a comparative genomic analysis was reported. For the purpose of this study, we call this gene, A.b_hyp gene. The aim of this study was to report the results of screening for the presence of the A.b_hyp gene in a worldwide collection of well-characterized A. baumannii collected from clinical and animal specimens. A total of 83 clinical, animal, and type strains were used. These comprised 73 A. baumannii isolates of clinical (n = 60) and animal origin (n = 13), and ten type strains, including a positive control strain, A. baumannii ATCC 19606. All isolates were examined by PCR amplification of the A.b_hyp gene. The A.b_hyp gene was detected in 72 isolates (99%) of A. baumannii but one clinical isolate failed to produce an amplicon. The control strain, A. baumannii ATCC 19606, was also positive for this gene. No bands were detected in non-A. baumannii species and therefore the isolates are thought to be negative for the gene. No bands were detected in non-A. baumannii isolates and therefore they are thought to be negative for the gene. The PCR A.b_ hyp method provides evidence that detection of this gene can be used as a reliable, easy, and low-cost biomarker for A. baumannii identification.
鲍曼不动杆菌是一种臭名昭著的医院病原体,以其引发严重感染的能力而闻名,尤其是在重症监护病房。据报道,在一项比较基因组分析中,发现了一个在鲍曼不动杆菌分离株中编码假定蛋白的保守基因,而在其他不动杆菌属物种中则没有。为了本研究的目的,我们将这个基因称为A.b_hyp基因。本研究的目的是报告在从临床和动物标本中收集的全球范围内特征明确的鲍曼不动杆菌中筛选A.b_hyp基因存在情况的结果。总共使用了83株临床、动物和标准菌株。其中包括73株临床来源(n = 60)和动物来源(n = 13)的鲍曼不动杆菌分离株,以及10株标准菌株,包括阳性对照菌株鲍曼不动杆菌ATCC 19606。通过对A.b_hyp基因进行PCR扩增对所有分离株进行检测。在72株(99%)鲍曼不动杆菌分离株中检测到了A.b_hyp基因,但有一株临床分离株未能产生扩增子。对照菌株鲍曼不动杆菌ATCC 19606对该基因也呈阳性。在非鲍曼不动杆菌物种中未检测到条带,因此这些分离株被认为该基因呈阴性。PCR A.b_hyp方法提供了证据,表明该基因的检测可作为鲍曼不动杆菌鉴定的可靠、简便且低成本的生物标志物。