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DOI 10.1016/s2666-5247(22)00158-6

Медицинская библиотека · The Lancet. Microbe · 2022

Emergence of a multidrug-resistant and virulent Streptococcus pneumoniae lineage mediates serotype replacement after PCV13: an international whole-genome sequencing study.

Lo Stephanie W, Mellor Kate, Cohen Robert, Alonso Alba Redin, Belman Sophie, Kumar Narender, Hawkins Paulina A, Gladstone Rebecca A, von Gottberg Anne, Veeraraghavan Balaji, Ravikumar K L, Kandasamy Rama, Pollard Sir Andrew J, Saha Samir K, Bigogo Godfrey, Antonio Martin, Kwambana-Adams Brenda, Mirza Shaper, Shakoor Sadia, Nisar Imran, Cornick Jennifer E, Lehmann Deborah, Ford Rebecca L, Sigauque Betuel, Turner Paul, Moïsi Jennifer, Obaro Stephen K, Dagan Ron, Diawara Idrissa, Skoczyńska Anna, Wang Hui, Carter Philip E, Klugman Keith P, Rodgers Gail, Breiman Robert F, McGee Lesley, Bentley Stephen D, Muñoz-Almagro Carmen, Varon Emmanuelle, Global Pneumococcal Sequencing Consortium

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Аннотация

BACKGROUND

Serotype 24F is one of the emerging pneumococcal serotypes after the introduction of pneumococcal conjugate vaccine (PCV). We aimed to identify lineages driving the increase of serotype 24F in France and place these findings into a global context.

METHODS

Whole-genome sequencing was performed on a collection of serotype 24F pneumococci from asymptomatic colonisation (n=229) and invasive disease (n=190) isolates among individuals younger than 18 years in France, from 2003 to 2018. To provide a global context, we included an additional collection of 24F isolates in the Global Pneumococcal Sequencing (GPS) project database for analysis. A Global Pneumococcal Sequence Cluster (GPSC) and a clonal complex (CC) were assigned to each genome. Phylogenetic, evolutionary, and spatiotemporal analysis were conducted using the same 24F collection and supplemented with a global collection of genomes belonging to the lineage of interest from the GPS project database (n=25 590).

FINDINGS: Serotype 24F was identified in numerous countries mainly due to the clonal spread of three lineages: GPSC10 (CC230), GPSC16 (CC156), and GPSC206 (CC7701). GPSC10 was the only multidrug-resistant lineage. GPSC10 drove the increase in 24F in France and had high invasive disease potential. The international dataset of GPSC10 (n=888) revealed that this lineage expressed 16 other serotypes, with only six included in 13-valent PCV (PCV13). All serotype 24F isolates were clustered in a single clade within the GPSC10 phylogeny and long-range transmissions were detected from Europe to other continents. Spatiotemporal analysis showed GPSC10-24F took 3-5 years to spread across France and a rapid change of serotype composition from PCV13 serotype 19A to 24F during the introduction of PCV13 was observed in neighbouring country Spain.

INTERPRETATION: Our work reveals that GPSC10 alone is a challenge for serotype-based vaccine strategy. More systematic investigation to identify lineages like GPSC10 will better inform and improve next-generation preventive strategies against pneumococcal diseases.

FUNDING: Bill & Melinda Gates Foundation, Wellcome Sanger Institute, and the US Centers for Disease Control and Prevention.

Для цитирования: Lo Stephanie W, Mellor Kate, Cohen Robert, Alonso Alba Redin, Belman Sophie, Kumar Narender, Hawkins Paulina A, Gladstone Rebecca A, von Gottberg Anne, Veeraraghavan Balaji, Ravikumar K L, Kandasamy Rama, Pollard Sir Andrew J, Saha Samir K, Bigogo Godfrey, Antonio Martin, Kwambana-Adams Brenda, Mirza Shaper, Shakoor Sadia, Nisar Imran, Cornick Jennifer E, Lehmann Deborah, Ford Rebecca L, Sigauque Betuel, Turner Paul, Moïsi Jennifer, Obaro Stephen K, Dagan Ron, Diawara Idrissa, Skoczyńska Anna, Wang Hui, Carter Philip E, Klugman Keith P, Rodgers Gail, Breiman Robert F, McGee Lesley, Bentley Stephen D, Muñoz-Almagro Carmen, Varon Emmanuelle, Global Pneumococcal Sequencing Consortium. Emergence of a multidrug-resistant and virulent Streptococcus pneumoniae lineage mediates serotype replacement after PCV13: an international whole-genome sequencing study.. The Lancet. Microbe. 2022. DOI: 10.1016/s2666-5247(22)00158-6.

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