Key features of pneumococcal isolates recovered in Central and Northwestern Russia in 2011–2018 determined through whole-genome sequencing

Author:

Egorova Ekaterina1ORCID,Kumar Narender2,Gladstone Rebecca A.32,Urban Yulia1,Voropaeva Elena1,Chaplin A.V.1,Rumiantseva Elena4,Svistunova T. S.5,Hawkins Paulina A.6,Klugman Keith P.7,Breiman Robert F.8,McGee Lesley6,Bentley Stephen D.92,Lo Stephanie W.2

Affiliation:

1. G. N. Gabrichevsky Research Institute for Epidemiology and Microbiology, Moscow, Russia

2. Parasites and Microbes, Wellcome Sanger Institute, Hinxton, UK

3. Department of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway

4. Labstory Medical Center, Saint Petersburg, Russia

5. Infectious Clinical Hospital № 2, Moscow, Russia

6. Centers for Disease Control and Prevention, Atlanta, USA

7. Rollins School of Public Health, Emory University, Atlanta, Georgia, USA

8. Emory Global Health Institute, Atlanta, USA

9. Department of Pathology, University of Cambridge, Cambridge, UK

Abstract

Invasive pneumococcal disease remains one of the leading causes of morbidity and mortality worldwide. In Russia, 13- valent pneumococcal conjugate vaccine (PCV13) was introduced into the childhood immunization programme nationwide in 2014. As part of the Global Pneumococcal Sequencing Project (GPS), we used genome data to characterize 179 pneumococcal isolates collected from Russia in 2011–2018 to investigate the circulating pneumococcal strains using a standardized genomic definition of pneumococcal lineages (global pneumococcal sequence clusters, GPSCs), prevalent serotypes and antimicrobial resistance profiles. We observed high serotype and lineage diversity among the 179 isolates recovered from cerebrospinal fluid (n=77), nasopharyngeal swabs (n=99) and other non-sterile site swabs (n=3). Overall, 60 GPSCs were identified, including 48 clonal complexes (CCs) and 14 singletons, and expressed 42 serotypes (including non-typable). Among PCV13 serotypes, 19F, 6B and 23F were the top three serotypes while 11A, 15B/C and 8 were the top three among non-PCV13 serotypes in the collection. Two lineages (GPSC6 and GPSC47) expressed both PCV13 and non-PCV13 serotypes that caused invasive disease, and were penicillin- and multidrug-resistant (MDR), highlighting their potential to adapt and continue to cause infections under vaccine and antibiotic selective pressure. PCV13 serotypes comprised 92 % (11/12) of the CSF isolates from the children aged below 5 years; however, the prevalence of PCV13 serotype isolates dropped to 53 % (31/58) among the nasopharyngeal isolates. Our analysis showed that 59 % (105/179) of the isolates were predicted to be non-susceptible to at least one class of antibiotics and 26 % (46/179) were MDR. Four MDR lineages (GPSC1, GPSC6, GPSC10 and GPSC47) accounted for 65 % (30/46) of the MDR isolates and expressed PCV13 serotypes (93 %, 28/30). This study provides evidence of high genetic and serotype diversity contributed by a mix of globally spreading and regionally circulating lineages in Russia. The observations suggest that the PCV13 vaccine could be important in reducing both invasive disease and antimicrobial resistance. We also identify potential lineages (GPSC6 and GPSC47) that may evade the vaccine.

Publisher

Microbiology Society

Subject

General Medicine

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