PLoS Pathogens (Apr 2023)

Genomic analysis unveils genome degradation events and gene flux in the emergence and persistence of S. Paratyphi A lineages.

  • Jobin John Jacob,
  • Agila K Pragasam,
  • Karthick Vasudevan,
  • Aravind Velmurugan,
  • Monisha Priya Teekaraman,
  • Tharani Priya Thirumoorthy,
  • Pallab Ray,
  • Madhu Gupta,
  • Arti Kapil,
  • Sulochana Putil Bai,
  • Savitha Nagaraj,
  • Karnika Saigal,
  • Temsunaro Rongsen Chandola,
  • Maria Thomas,
  • Ashish Bavdekar,
  • Sheena Evelyn Ebenezer,
  • Jayanthi Shastri,
  • Anuradha De,
  • Shantha Dutta,
  • Anna P Alexander,
  • Roshine Mary Koshy,
  • Dasaratha R Jinka,
  • Ashita Singh,
  • Sunil Kumar Srivastava,
  • Shalini Anandan,
  • Gordon Dougan,
  • Jacob John,
  • Gagandeep Kang,
  • Balaji Veeraraghavan,
  • Ankur Mutreja

DOI
https://doi.org/10.1371/journal.ppat.1010650
Journal volume & issue
Vol. 19, no. 4
p. e1010650

Abstract

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Paratyphoid fever caused by S. Paratyphi A is endemic in parts of South Asia and Southeast Asia. The proportion of enteric fever cases caused by S. Paratyphi A has substantially increased, yet only limited data is available on the population structure and genetic diversity of this serovar. We examined the phylogenetic distribution and evolutionary trajectory of S. Paratyphi A isolates collected as part of the Indian enteric fever surveillance study "Surveillance of Enteric Fever in India (SEFI)." In the study period (2017-2020), S. Paratyphi A comprised 17.6% (441/2503) of total enteric fever cases in India, with the isolates highly susceptible to all the major antibiotics used for treatment except fluoroquinolones. Phylogenetic analysis clustered the global S. Paratyphi A collection into seven lineages (A-G), and the present study isolates were distributed in lineages A, C and F. Our analysis highlights that the genome degradation events and gene acquisitions or losses are key molecular events in the evolution of new S. Paratyphi A lineages/sub-lineages. A total of 10 hypothetically disrupted coding sequences (HDCS) or pseudogenes-forming mutations possibly associated with the emergence of lineages were identified. The pan-genome analysis identified the insertion of P2/PSP3 phage and acquisition of IncX1 plasmid during the selection in 2.3.2/2.3.3 and 1.2.2 genotypes, respectively. We have identified six characteristic missense mutations associated with lipopolysaccharide (LPS) biosynthesis genes of S. Paratyphi A, however, these mutations confer only a low structural impact and possibly have minimal impact on vaccine effectiveness. Since S. Paratyphi A is human-restricted, high levels of genetic drift are not expected unless these bacteria transmit to naive hosts. However, public-health investigation and monitoring by means of genomic surveillance would be constantly needed to avoid S. Paratyphi A serovar becoming a public health threat similar to the S. Typhi of today.