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First hybrid complete genome of Aeromonas veronii reveals chromosome-mediated novel structural variant mcr-3.30 from a human clinical sample.

Naveen Kumar Devanga RagupathiDhiviya Prabaa Muthuirulandi SethuvelShalini AnandanDhivya MuruganKalaiarasi AsokanRamya Gajaraj Neethi MohanKarthick VasudevanThirumal Kumar DGeorge Priya Doss CBalaji Veeraraghavan
Published in: Access microbiology (2020)
Recent findings demonstrate the origin of the plasmid-mediated colistin resistance gene mcr-3 from aeromonads. The present study aimed to screen for plasmid-mediated colistin resistance among 30 clinical multidrug-resistant (MDR) Aeromonas spp. PCR was used to screen for the presence of mcr-1, mcr-2, mcr-3 and mcr-4, which revealed mcr-3 in a colistin-susceptible isolate (FC951). All other isolates were negative for mcr. Sequencing of FC951 revealed that the mcr-3 (mcr-3.30) identified was different from previously reported variants and had 95.62 and 95.28 % nucleotide similarity with mcr-3.3 and mcr-3.10. Hybrid assembly using IonTorrent and MinION reads revealed structural genetic information for mcr-3.30 with an insertion of ISAs18 within the gene. Due to this, mcr-3.30 was non-expressive, which makes FC951 susceptible to colistin. Further, in silico sequence and protein structural analysis confirmed the new variant. To the best of our knowledge, this is the first report on a novel mcr-3 variant from India. The significant role of mcr-like genes in different Aeromonas species remains unknown and requires additional investigation to obtains insights into the mechanism of colistin resistance.
Keyphrases
  • escherichia coli
  • multidrug resistant
  • klebsiella pneumoniae
  • acinetobacter baumannii
  • gram negative
  • drug resistant
  • healthcare
  • genome wide
  • single cell
  • endothelial cells
  • high throughput
  • cystic fibrosis
  • binding protein