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Sequencing and Characterization of Strain UM869: A Comprehensive Comparative Genomic Analysis of Virulence, Antibiotic Resistance, and Functional Pathways. | LitMetric

AI Article Synopsis

  • UM869 is a Gram-negative pathogen that is resistant to colistin and is linked to various infections both in hospitals and the community.
  • The study explored virulence factors and resistance mechanisms in UM869, discovering it has 65 virulence-related genes and 11 genes contributing to antibiotic resistance.
  • Comparative genomic analysis indicated a strong genetic similarity (98.37%) among UM869 and 79 other genomes, with implications for spreading resistance and virulence, primarily in Asian regions, emphasizing the need for better monitoring and treatment strategies.

Article Abstract

is a Gram-negative opportunistic pathogen inherently resistant to colistin. This species causes various clinical and community-acquired infections. This study investigated the virulence factors, resistance mechanisms, functional pathways, and comparative genomic analysis of strain UM869 with 79 publicly available genomes. The multidrug resistance strain UM869 harbored 65 genes associated with 30 virulence factors, including efflux pump, hemolysin, urease, adherence, toxin, and endotoxin. Additionally, this strain contained 11 genes related to target alteration, antibiotic inactivation, and efflux resistance mechanisms. Further, the comparative genomic study revealed a high genetic relatedness (98.37%) among the genomes, possibly due to the dissemination of genes between adjoining countries. The core proteome of 79 genomes contains the 2692 core, including 2447 single-copy orthologues. Among them, six were associated with resistance to major antibiotic classes manifested through antibiotic target alteration (, ) and antibiotic efflux (, , ; ; ). Similarly, 47 core orthologues were annotated to 27 virulence factors. Moreover, mostly core orthologues were mapped to transporters ( = 576), two-component systems ( = 148), transcription factors ( = 117), ribosomes ( = 114), and quorum sensing ( = 77). The presence of diversity in serotypes (type 2, 3, 6, 8, and 11) and variation in gene content adds to the pathogenicity, making them more difficult to treat. This study highlights the genetic similarity among the genomes of and their restricted emergence, mostly in Asian countries, in addition to their growing pathogenicity and resistance. However, steps must be taken to undertake large-scale molecular surveillance and to direct suitable therapeutic interventions.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10298637PMC
http://dx.doi.org/10.3390/genes14061279DOI Listing

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