Molecular Analysis of Whole Genomic Sequencing for Acinetobacter Baumannii Isolates under Antibiotic Stress in a Hospital Outbreak
Abstract
Introduction: A study was conducted to identify specialised genes in two types of Acinetobacter baumannii, namely MDR, XDR, and PDR. These genes may play a crucial role in the ability of these species to coexist with the human host and show a wide range of diversity in genes that contribute to antibiotic resistance and lipopolysaccharide barrier.
Methodology: The identification of 70 A. baumannii isolates was carried out through morphology and culture on CHROM agar, followed by biochemical testing. Genotypic identification was performed using
16S rRNA and blaOxa-51 gene for A. baumannii species. Based on the antibiotic resistance categories, two isolates (AB32 and AB51) were selected for whole genome sequencing (WGS) using Illumina MiSeq technology. The analysis identified specialised genes in these isolates that contribute to antibiotic stress and lipopolysaccharide barrier, including complex sets of partial and complete integrons and
transposons.
Results: The recent findings showed that A. baumannii exhibits the highest resistance to gatifloxacin. The genome analysis revealed that AB3, AB32, and AB51 belong to unique STs (ST/1418, and ST/441), while AB R75 belongs to a known international clone of a high-risk strain (ST/195). The presence of efflux pump genes EmrAB-TolC, MacA, MacB, MdfA/ Cmr, TolC/ OpmH, and atG catalase gene encoding an
antibiotic activation enzyme was identified in the WGS results. In addition, antibiotic target protection and replacement proteins that confer resistance against gatifloxacin and colistin sulphates were encoded by BcrC, FabG, and HtdX genes.
Conclusions: Our study provided a detailed genomic picture of both innate and acquired plasmid-encoded AMR genes.
How to cite this article:
Abed ES, Ali MR. Molecular Analysis of Whole
Genomic Sequencing for Acinetobacter
Baumannii Isolates under Antibiotic Stress
in a Hospital Outbreak. J Commun Dis.
2024;56(1):106-119.
DOI: https://doi.org/10.24321/0019.5138.202415
References
Kurcik-Trajkovska B. Acinetobacter spp.-a serious enemy threatening hospitals worldwide. Maced J Med
Sci. 2009;2(2):157-62. [Google Scholar]
Garnacho-Montero J, Timsit JF. Managing Acinetobacter baumannii infections. Curr Opin Infect Dis. 2019;32(1):69-76. [PubMed] [Google Scholar]
Bardbari AM, Mohajeri P, Arabestani MR, Karami M, Keramat F, Asadollahi S, Khodavirdipour A, Alikhani MY.
Molecular typing of multi-drug resistant Acinetobacter baumannii isolates from clinical and environmental specimens in three Iranian hospitals by pulsed field gel electrophoresis. BMC Microbiol. 2020;20(1):101.
[PubMed] [Google Scholar]
Adams MD, Goglin K, Molyneaux N, Hujer KM, Lavender H, Jamison JJ, MacDonald IJ, Martin KM, Russo T, Campagnari AA, Hujer AM, Bonomo RA, Gill SR. Comparative genome sequence analysis of multidrug-resistant Acinetobacter baumannii. J Bacteriol. 2008;190(24):8053-64. [PubMed] [Google Scholar]
Imperi F, Antunes LC, Blom J, Villa L, Iacono M, Visca P, Carattoli A. The genomics of Acinetobacter baumannii:
insights into genome plasticity, antimicrobial resistance and pathogenicity. IUBMB Life. 2011;63(12):1068-74.
[PubMed] [Google Scholar]
Bartual SG, Seifert H, Hippler C, Luzon MA, Wisplinghoff
H, Rodriguez-Valera F. Development of a multilocus sequence typing scheme for characterization of clinical isolates of Acinetobacter baumannii. J Clin Microbiol. 2005;43(9):4382-90. [PubMed] [Google Scholar]
Diancourt L, Passet V, Nemec A, Dijkshoorn L, Brisse S. The population structure of Acinetobacter baumannii:
expanding multiresistant clones from an ancestral susceptible genetic pool. PloS One. 2010;5(4):e10034.
[PubMed] [Google Scholar]
Copyright (c) 2024 Journal of Communicable Diseases (E-ISSN: 2581-351X & P-ISSN: 0019-5138)
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.