Background
Serratia marcescens may cause rare central nervous system infections. The growing antibiotic resistance in these isolates makes treatment challenging. S. marcescens (MIID-C14) was isolated from the cerebrospinal fluid of a 56-year-old female patient admitted to Salmaniya Medical Complex, Bahrain. Due to the virulence and multidrug resistance exhibited by this bacterium, we aimed to analyse the genetic makeup of this isolate.
Methods
The isolate was identified via MALDI-TOF mass spectrometry, antimicrobial susceptibility was performed by VITEK-2 system, and whole-genome sequencing (WGS) was conducted on the Illumina Novoseq 6000 S4 platform. The genome was annotated using the Prokaryotic Genome Annotation Pipeline (NCBI). In-silico predictions of antibiotic resistance genes, virulence genes, and multilocus sequence typing were performed using curated bioinformatics tools.
Results
MIID-C14 showed resistance to cefotaxime, ceftazidime, cefepime, and ertapenem, and was sensitive to gentamicin, ciprofloxacin, and trimethoprim/sulfamethoxazole. The complete genome of MIID-C14 was 4983,593 bp with 60.2 % GC content, and a Benchmarking Universal Single-Copy Orthologs score of 100. Molecular analysis identified antibiotic resistance genes for aminoglycosides (aac(6′)), fluoroquinolones (oqxB), Diaminopyrimidine/Sulfonamides (sul), and a chromosomal beta-lactamase (SRT-2). Multilocus sequence typing identified the sequence type as ST-367. Additionally, the genome harbored 218 mobile genetic elements, including 98 instances of horizontal gene transfer, and two virulence genes (fliM and rcsB). WGS data of this strain are available in the NCBI database under the BioProject: PRJNA1113219, BioSample: SAMN41450192, GenBank Accession: JBDXSY000000000.
Conclusion
To our knowledge, this is the first report of S. marcescens ST-367 in the Gulf Cooperation Council. The genetic diversity and mechanisms of virulence and antibiotic resistance in this isolate shed light on the evolution of high-risk isolates. Additionally, this will serve as a foundation for future extensively drug-resistant isolates.
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