Affiliations 

  • 1 Department of Biological Sciences, Birla Institute of Technology and Science (BITS), Pilani, Rajasthan, India. p20180406@pilani.bits-pilani.ac.in
  • 2 Department of Biological Sciences, Birla Institute of Technology and Science (BITS), Pilani, Rajasthan, India
  • 3 Department of Biological Sciences, Sunway University, Petaling Jaya, Selangor, Malaysia
  • 4 Department of Biological Sciences, Birla Institute of Technology and Science (BITS), Pilani, Rajasthan, India. sandhya.marathe@pilani.bits-pilani.ac.in
Sci Rep, 2020 12 03;10(1):21156.
PMID: 33273523 DOI: 10.1038/s41598-020-77890-6

Abstract

Salmonellae display intricate evolutionary patterns comprising over 2500 serovars having diverse pathogenic profiles. The acquisition and/or exchange of various virulence factors influences the evolutionary framework. To gain insights into evolution of Salmonella in association with the CRISPR-Cas genes we performed phylogenetic surveillance across strains of 22 Salmonella serovars. The strains differed in their CRISPR1-leader and cas operon features assorting into two main clades, CRISPR1-STY/cas-STY and CRISPR1-STM/cas-STM, comprising majorly typhoidal and non-typhoidal Salmonella serovars respectively. Serovars of these two clades displayed better relatedness, concerning CRISPR1-leader and cas operon, across genera than between themselves. This signifies the acquisition of CRISPR1/Cas region could be through a horizontal gene transfer event owing to the presence of mobile genetic elements flanking CRISPR1 array. Comparison of CRISPR and cas phenograms with that of multilocus sequence typing (MLST) suggests differential evolution of CRISPR/Cas system. As opposed to broad-host-range, the host-specific serovars harbor fewer spacers. Mapping of protospacer sources suggested a partial correlation of spacer content with habitat diversity of the serovars. Some serovars like serovar Enteritidis and Typhimurium that inhabit similar environment/infect similar hosts hardly shared their protospacer sources.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.