Population structure and antimicrobial resistance patterns of Salmonella Typhi and Paratyphi A amid a phased municipal vaccination campaign in Navi Mumbai, India

Author:

da Silva Kesia Esther1ORCID,Date Kashmira2,Hirani Nilma3,LeBoa Christopher4,Jayaprasad Niniya5,Borhade Priyanka5,Warren Joshua6,Shimpi Rahul5,Hoffman Seth A.1,Mikoleit Matthew2,Bhatnagar Pankaj5,Cao Yanjia7,Haldar Pradeep8,Harvey Pauline5,Zhang Chenhua2,Daruwalla Savita9,Dharmapalan Dhanya10,Gavhane Jeetendra11,Joshi Shrikrishna12,Rai Rajesh13,Rathod Varsha14,Shetty Keertana15,Warrier Divyalatha S.16,Yadav Shalini17,Chakraborty Debjit18,Bahl Sunil19,Katkar Arun5,Kunwar Abhishek5,Yewale Vijay10,Dutta Shanta18,Luby Stephen P.1,Andrews Jason R.1ORCID

Affiliation:

1. Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine , Stanford, California, USA

2. Centers for Disease Control and Prevention , Atlanta, Georgia, USA

3. Grant Government Medical College & Sir J J Hospital , Mumbai, Maharashtra, India

4. Division of Environmental Health Sciences, School of Public Health, University of California , Berkeley, California, USA

5. World Health Organization-Country Office for India, National Public Health Surveillance Project , New Delhi, India

6. Yale School of Public Health, Yale University , New Haven, Connecticut, USA

7. Department of Geography, The University of Hong Kong , Hong Kong

8. Ministry of Health & Family Welfare, Government of India , New Delhi, India

9. Department of Pediatrics, NMMC General Hospital , Navi Mumbai, India

10. Dr. Yewale Multispecialty Hospital for Children , Navi Mumbai, India

11. Department of Pediatrics, MGM New Bombay Hospital, MGM Medical College , Navi Mumbai, India

12. Dr. Joshi’s Central Clinical Microbiology Laboratory , Navi Mumbai, India

13. Department of Pediatrics & Neonatology, Dr. D.Y. Patil Medical College and Hospital , Navi Mumbai, India

14. Rajmata Jijau Hospital, Airoli (NMMC) , Navi Mumbai, India

15. Department of Microbiology, Dr. D.Y. Patil Medical College and Hospital , Navi Mumbai, India

16. Department of Pediatrics, Mathadi Trust Hospital , Navi Mumbai, India

17. Department of Microbiology, MGM New Bombay Hospital , Navi Mumbai, India

18. National Institute of Cholera and Enteric Diseases, Indian Council of Medical Research , Kolkata, India

19. World Health Organization South-East Asia Regional Office , New Delhi, India

Abstract

ABSTRACT We performed whole-genome sequencing of 174 Salmonella Typhi and 54 Salmonella Paratyphi A isolates collected through prospective surveillance in the context of a phased typhoid conjugate vaccine introduction in Navi Mumbai, India. We investigate the temporal and geographical patterns of emergence and spread of antimicrobial resistance. We evaluated the relationship between the spatial distance between households and genetic clustering of isolates. Most isolates were non-susceptible to fluoroquinolones, with nearly 20% containing ≥3 quinolone resistance-determining region mutations. Two H58 isolates carried an IncX3 plasmid containing bla SHV-12 , associated with ceftriaxone resistance, suggesting that the ceftriaxone-resistant isolates from India independently evolved on multiple occasions. Among S . Typhi, we identified two main clades circulating (2.2 and 4.3.1 [H58]); 2.2 isolates were closely related following a single introduction around 2007, whereas H58 isolates had been introduced multiple times to the city. Increasing geographic distance between isolates was strongly associated with genetic clustering (odds ratio [OR] = 0.72 per km; 95% credible interval [CrI]: 0.66–0.79). This effect was seen for distances up to 5 km (OR = 0.65 per km; 95% CrI: 0.59–0.73) but not seen for distances beyond 5 km (OR = 1.02 per km; 95% CrI: 0.83–1.26). There was a non-significant reduction in odds of clustering for pairs of isolates in vaccination communities compared with non-vaccination communities or mixed pairs compared with non-vaccination communities. Our findings indicate that S . Typhi was repeatedly introduced into Navi Mumbai and then spread locally, with strong evidence of spatial genetic clustering. In addition to vaccination, local interventions to improve water and sanitation will be critical to interrupt transmission. IMPORTANCE Enteric fever remains a major public health concern in many low- and middle-income countries, as antimicrobial resistance (AMR) continues to emerge. Geographical patterns of typhoidal Salmonella spread, critical to monitoring AMR and planning interventions, are poorly understood. We performed whole-genome sequencing of S . Typhi and S . Paratyphi A isolates collected in Navi Mumbai, India before and after a typhoid conjugate vaccine introduction. From timed phylogenies, we found two dominant circulating lineages of S . Typhi in Navi Mumbai-lineage 2.2, which expanded following a single introduction a decade prior, and 4.3.1 (H58), which had been introduced repeatedly from other parts of India, frequently containing “triple mutations” conferring high-level ciprofloxacin resistance. Using Bayesian hierarchical statistical models, we found that spatial distance between cases was strongly associated with genetic clustering at a fine scale (<5 km). Together, these findings suggest that antimicrobial-resistant S . Typhi frequently flows between cities and then spreads highly locally, which may inform surveillance and prevention strategies.

Funder

Bill and Melinda Gates Foundation

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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