Analysis of the Class 1 Integrons, Carbapenemase Genes and Biofilm Formation Genes Occurrence in Acinetobacter baumannii Clinical Isolates.

Autor: Xiu Y; 1Department of Laboratory Medicine, Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China., Dai Y; 1Department of Laboratory Medicine, Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China., Yin S; 1Department of Laboratory Medicine, Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China., Wei Q; 1Department of Laboratory Medicine, Anhui University of Science and Technology Affiliated Fengxian Hospital, Shanghai, China.; 2Department of Laboratory Medicine, Southern Medical University Affiliated Fengxian Hospital, Shanghai, China.; 3Department of Laboratory Medicine, Shanghai University of Medicine and Health Sciences Affiliated Sixth People's Hospital South Campus, Shanghai, China.
Jazyk: angličtina
Zdroj: Polish journal of microbiology [Pol J Microbiol] 2024 May 29; Vol. 73 (2), pp. 189-197. Date of Electronic Publication: 2024 May 29 (Print Publication: 2024).
DOI: 10.33073/pjm-2024-017
Abstrakt: Acinetobacter baumannii is a non-fermentative Gram-negative bacterium that can cause nosocomial infections in critically ill patients. Carbapenem-resistant A. baumannii (CRAB) has spread rapidly in clinical settings and has become a key concern. The main objective of this study was to identify the distribution of integrons and biofilm-formation-related virulence genes in CRAB isolates. A total of 269 A. baumannii isolates (219 isolates of CRAB and 50 isolates of carbapenem-sensitive A. baumannii (CSAB)) were collected. Carbapenemase genes ( bla KPC , bla VIM , bla IMP , bla NDM , and bla OXA-23-like ) and biofilm-formation-related virulence genes ( abal , bfms , bap , and cusE ) were screened with PCR. Class 1 integron was screened with PCR, and common promoters and gene cassette arrays were determined with restriction pattern analysis combined with primer walking sequencing. Whole-genome sequencing was conducted, and data were analyzed for a bla OXA-23-like -negative isolate. All 219 CRAB isolates were negative for bla KPC , bla VIM , bla IMP , and bla NDM , while bla OXA-23-like was detected in 218 isolates. The detection rates for abal , bfms , bap , and cusE in 219 CRAB were 93.15%, 63.93%, 88.13%, and 77.63%, respectively. Class 1 integron was detected in 75 CRAB (34.25%) and in 3 CSAB. The single gene cassette array aacA4-catB8-aadA1 with relatively strong PcH2 promoter was detected in class 1 integrons. The bla OXA-23-like -negative CRAB isolate was revealed to be a new sequence type (Oxford 3272, Pasteur 2520) carrying bla OXA-72 , bla OXA-259 , and bla ADC-26 . In conclusion, bla OXA-23-like was the main reason for CRAB's resistance to carbapenems. A new (Oxford 3272, Pasteur 2520) CRAB sequence type carrying the bla OXA-72 , bla OXA-259 , and bla ADC-26 was reported.
(© 2024 Yu Xiu et al., published by Sciendo.)
Databáze: MEDLINE
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