Three novel multiplex PCR assays for rapid detection of virulence, antimicrobial resistance, and toxin genes in Acinetobacter calcoaceticus-baumannii complex species

生物 鲍曼不动杆菌 多重聚合酶链反应 微生物学 毒力 钙不动杆菌 抗菌剂 多路复用 基因 毒素 不动杆菌 抗生素耐药性 聚合酶链反应 细菌 遗传学 抗生素 铜绿假单胞菌
作者
Alexander A Sheikh,Danielle Schneiderman,Ellen M. E. Sykes,Ayush Kumar,Wen Chen,David R. Lapen,Izhar U. H. Khan
出处
期刊:Letters in Applied Microbiology [Oxford University Press]
卷期号:77 (3) 被引量:1
标识
DOI:10.1093/lambio/ovae027
摘要

The Acinetobacter calcoaceticus-baumannii (ACB) complex is an often-overlooked group of nosocomial pathogens with a significant environmental presence. Rapid molecular screening methods for virulence, antimicrobial resistance, and toxin (VAT) genes are required to investigate the potential pathogenicity of environmental isolates. This study aimed to develop and apply novel ACB complex-specific multiplex PCR (mPCR) primers and protocols for the rapid detection of eight VAT genes. We optimized three single-tube mPCR assays using reference DNA from ACB complex and other Acinetobacter species. These assays were then applied to detect VAT genes in cultured ACB complex isolates recovered from clinical and environmental sources. Widespread detection of VAT genes in environmental isolates confirmed the validity, functionality, and applicability of these novel assays. Overall, the three newly developed ACB complex species-specific mPCR assays are rapid and simple tools that can be adopted in diagnostic and clinical lab settings. The detection of VAT genes in environmental isolates suggests that environmental niches could serve as a reservoir for potentially pathogenic ACB complex and warrants further investigation. The newly developed mPCR assays are specific, sensitive, and efficient, making them well-suited for high-throughput screening in epidemiological studies and evaluating the potential pathogenicity of ACB complex recovered from various sources.
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