Phylogenomic investigation of an outbreak of fluoroquinolone-resistant Salmonella enterica subsp. enterica serovar Paratyphi A in Phnom Penh, Cambodia

Author:

Dusadeepong Rutaiwan12,Delvallez Gauthier1,Cheng Sokleaph31,Meng Soda1,Sreng Navin4,Letchford Joanne5,Choun Kimcheng6,Teav Syna7,Hardy Liselotte8,Jacobs Jan98,Hoang Tuyet1011,Seemann Torsten1011,Howden Benjamin P.1011,Glaser Philippe12,Stinear Timothy P.10,Vandelannoote Koen12ORCID

Affiliation:

1. Medical Biology Laboratory, Pasteur Institute of Cambodia, Phnom Penh, Cambodia

2. Bacterial Phylogenomics Group, Pasteur Institute of Cambodia, Phnom Penh, Cambodia

3. LMI Drug Resistance in South East Asia, Pasteur Institute of Cambodia, Phnom Penh, Cambodia

4. Laboratory of Environment and Food Safety, Pasteur Institute of Cambodia, Phnom Penh, Cambodia

5. Diagnostic Microbiology Development Program, Phnom Penh, Cambodia

6. Infectious Disease Department, Sihanouk Hospital Center of HOPE, Phnom Penh, Cambodia

7. Laboratory Unit, Sihanouk Hospital Center of HOPE, Phnom Penh, Cambodia

8. Department of Clinical Sciences, Institute of Tropical Medicine, Antwerp, Belgium

9. Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium

10. Centre for Pathogen Genomics, Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

11. Microbiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

12. Evolution and Ecology of Antibiotic Resistance Unit, APHP–CNRS–UMR6047, Institut Pasteur–University Paris-Saclay–Université Paris Cité, Paris, France

Abstract

In early 2020, the Medical Biology Laboratory of the Pasteur Institute of Cambodia isolated an unusually high number of fluoroquinolone-resistant Salmonella enterica subspecies enterica serovar Paratyphi A strains during its routine bacteriological surveillance activities in Phnom Penh, Cambodia. A public-health investigation was supported by genome sequencing of these Paratyphi A strains to gain insights into the genetic diversity and population structure of a potential outbreak of fluoroquinolone-resistant paratyphoid fever. Comparative genomic and phylodynamic analyses revealed the 2020 strains were descended from a previously described 2013–2015 outbreak of Paratyphi A infections. Our analysis showed sub-lineage 2.3.1 had remained largely susceptible to fluoroquinolone drugs until 2015, but acquired chromosomal resistance to these drugs during six separate events between late 2012 and 2015. The emergence of fluoroquinolone resistance was rapidly followed by the replacement of the original susceptible Paratyphi A population, which led to a dramatic increase of fluoroquinolone-resistant blood-culture-confirmed cases in subsequent years (2016–2020). The rapid acquisition of resistance-conferring mutations in the Paratyphi A population over a 3 year period is suggestive of a strong selective pressure on that population, likely linked with fluoroquinolone use. In turn, emergence of fluoroquinolone resistance has led to increased use of extended-spectrum cephalosporins like ceftriaxone that are becoming the drug of choice for empirical treatment of paratyphoid fever in Cambodia.

Publisher

Microbiology Society

Subject

General Medicine

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