AUTHOR=Mancilla-Rojano Jetsi , Castro-Jaimes Semiramis , Ochoa Sara A. , Bobadilla del Valle Miriam , Luna-Pineda Victor M. , Bustos Patricia , Laris-González Almudena , Arellano-Galindo José , Parra-Ortega Israel , Hernández-Castro Rigoberto , Cevallos Miguel A. , Xicohtencatl-Cortes Juan , Cruz-Córdova Ariadnna 

TITLE=Whole-Genome Sequences of Five Acinetobacter baumannii Strains From a Child With Leukemia M2

JOURNAL=Frontiers in Microbiology

VOLUME=10

YEAR=2019

URL=https://www.frontiersin.org/journals/microbiology/articles/10.3389/fmicb.2019.00132

DOI=10.3389/fmicb.2019.00132

ISSN=1664-302X

ABSTRACT=<p><italic>Acinetobacter baumannii</italic> is an opportunistic pathogen and is one of the primary etiological agents of healthcare-associated infections (HAIs). <italic>A. baumannii</italic> infections are difficult to treat due to the intrinsic and acquired antibiotic resistance of strains of this bacterium, which frequently limits therapeutic options. In this study, five <italic>A. baumannii</italic> strains (810CP, 433H, 434H, 483H, and A-2), all of which were isolated from a child with leukemia M2, were characterized through antibiotic susceptibility profiling, the detection of genes encoding carbapenem hydrolyzing oxacillinases, pulsed-field gel electrophoresis (PFGE), multilocus sequence typing (MLST), adherence and invasion assays toward the A549 cell line, and the whole-genome sequence (WGS). The five strains showed Multidrug resistant (MDR) profiles and amplification of the <italic>bla</italic><sub>OXA-23</sub> gene, belonging to ST758 and grouped into two PFGE clusters. WGS of 810CP revealed the presence of a circular chromosome and two small plasmids, pAba810CPa and pAba810CPb. Both plasmids carried genes encoding the Sp1TA system, although resistance genes were not identified. A gene-by-gene comparison analysis was performed among the <italic>A. baumannii</italic> strains isolated in this study and others <italic>A</italic>. <italic>baumannii</italic> ST758 strains (HIMFG and INCan), showing that 86% of genes were present in all analyzed strains. Interestingly, the 433H, 434H, and 483H strains varied by 8–10 single-nucleotide variants (SNVs), while the A2 and 810CP strains varied by 46 SNVs. Subsequently, an analysis using BacWGSTdb showed that all of our strains had the same resistance genes and were ST758. However, some variations were observed in relation to virulence genes, mainly in the 810CP strain. The genes involved in the synthesis of hepta-acylated lipooligosaccharides, the <italic>pgaABCD</italic> locus encoding poly-β-1-6-<italic>N</italic>-acetylglucosamine, the <italic>ompA</italic> gene, Csu pili, <italic>bap</italic>, the two-component system <italic>bfms</italic>/<italic>bfmR</italic>, a member of the phospholipase D family, and two iron-uptake systems were identified in our <italic>A</italic>. <italic>baumannii</italic> strains genome. The five <italic>A. baumannii</italic> strains isolated from the child were genetically different and showed important characteristics that promote survival in a hospital environment. The elucidation of their genomic sequences provides important information for understanding their epidemiology, antibiotic resistance, and putative virulence factors.</p>