Evidence map›Paper›PMID 41286605›Full record

ArticleBMC microbiology2025

Evolution of pneumococcal serotype 19A in children in Bangladesh: insights from genomic analysis.

Arif Mohammad Tanmoy, Esha Kazi, Naito Kanon, Hafizur Rahman, Harry C H Hung, Md Hasanuzzaman, Roly Malaker, Apurba Rajib Malaker, Deb Purna Keya, Sudipta Deb Nath and 9 more

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Arif Mohammad TanmoyChild Health Research Foundation, Dhaka, Bangladesh.
Esha KaziChild Health Research Foundation, Dhaka, Bangladesh.
Naito KanonChild Health Research Foundation, Dhaka, Bangladesh.
Hafizur RahmanChild Health Research Foundation, Dhaka, Bangladesh.
Harry C H HungParasites and Microbes, Wellcome Sanger Institute, Hinxton, UK.
Md HasanuzzamanChild Health Research Foundation, Dhaka, Bangladesh.
Roly MalakerChild Health Research Foundation, Dhaka, Bangladesh.
Apurba Rajib MalakerChild Health Research Foundation, Dhaka, Bangladesh.
Deb Purna KeyaChild Health Research Foundation, Dhaka, Bangladesh.
Sudipta Deb NathChild Health Research Foundation, Dhaka, Bangladesh.
Belal HossainChild Health Research Foundation, Dhaka, Bangladesh.
Shampa SahaChild Health Research Foundation, Dhaka, Bangladesh.
Mohammad Jamal UddinChild Health Research Foundation, Dhaka, Bangladesh.
Lesley McGeeCenters for Disease Control and Prevention, Atlanta, GA, USA.
Stephen D BentleyParasites and Microbes, Wellcome Sanger Institute, Hinxton, UK.
Stephanie W LoParasites and Microbes, Wellcome Sanger Institute, Hinxton, UK.
Yogesh HoodaChild Health Research Foundation, Dhaka, Bangladesh.
Samir K SahaChild Health Research Foundation, Dhaka, Bangladesh.
Senjuti SahaChild Health Research Foundation, Dhaka, Bangladesh. senjutisaha@chrfbd.org.

Funding

Bill and Melinda Gates Foundation OPP1024654Bill and Melinda Gates Foundation OPP1034556 and INV-003570GAVI Alliance 201588766, 201233523, 201022732, and 200749550Pfizer WI209075Sanofi Pasteur EPN00014
6 · The paper itself

Abstract

backgroundInvasive pneumococcal disease (IPD), caused by Streptococcus pneumoniae, remains a major global health concern, particularly for children. Among more than 100 pneumococcal serotypes, 19A is known for its multidrug resistance (MDR) and increased incidence following PCV7/PCV10 introduction in many countries. Bangladesh introduced PCV10 in 2015 considering the low burden of 19A in the country.

methodsUtilizing our IPD surveillance from 2004 to 2023, we investigated the hospital incidence of serotype 19A before and after PCV10 introduction among < 5 years old children in Bangladesh. Whole-genome sequencing was done for 153 serotype 19A isolates from IPD, otitis media, carriage, and urine samples. We used phylogenetic and BEAST analyses to investigate population structure, circulating subtypes, global pneumococcal sequence clusters (GPSCs), sequence types (STs), and antimicrobial resistance genes, and compared them with global 19A genomes.

resultsOur findings indicate no increase in hospital IPD incidence due to serotype 19A following PCV10 introduction. The MDR 19A-ST320 lineage (GPSC1) remains absent in Bangladesh. ST12888 (GPSC84) became dominant in the post-PCV10 introduction (from 15% to 70%). GPSC84 carries the capsular locus of 19A subtype-I (19A-I), which emerged independently from the standard 19A locus. Macrolide resistance is increasing within the 19A-I/GPSC84 lineage and is estimated to have originated between 2007 and 2011.

conclusionsThis study presents the first comprehensive genomic analysis of the serotype 19A population in Bangladesh, supporting the decision to introduce PCV10 in Bangladesh based on local pneumococcal serotype burden data. However, the rapid evolution within the local 19A population highlights the need for continuous epidemiological and genomic surveillance to support effective vaccination programs.

Indexed as

Evolution, MolecularPneumococcal InfectionsStreptococcus pneumoniaeAnti-Bacterial AgentsBangladeshChild, PreschoolDrug Resistance, Multiple, BacterialFemaleGenome, BacterialGenomicsHumansIncidenceInfantMalePhylogenyPneumococcal VaccinesAnti-Bacterial AgentsPneumococcal VaccinesBangladeshEvolutionGenomicsInvasive pneumococcal diseasePCV10Serotype 19AStreptococcus pneumoniae

Identifiers

PMID41286605
PMCPMC12642354

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.