Distribution of capsule and O types in Klebsiella pneumoniae causing neonatal sepsis in Africa and South Asia: A meta-analysis of genome-predicted serotype prevalence to inform potential vaccine coverage

Neonatal sepsis is associated with diverse K and O types, with substantial geographic and temporal variation even after adjusting for localised transmission clusters. Despite this, a single 20-valent K vaccine could theoretically cover ≥70% of infections in all target regions. Locally-targeted vaccines could achieve higher coverage with lower valency, but are less feasible. In principle, very high coverage could be achieved with lower valency O-based vaccines, however, the protective efficacy against disease of antibodies targeting the O antigen remains uncertain. Further research is needed on cross-reactivity, antigen exposure, and stability of antigens over time, to better inform vaccine development.

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Publication Details

Journal
PLoS Medicine
Published
2026-01-12
DOI
https://doi.org/10.1371/journal.pmed.1004879
Citations
1
Primary Topic
Neonatal and Maternal Infections
Type
article
Field-Weighted Citation Impact
41.85
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article

Distribution of capsule and O types in Klebsiella pneumoniae causing neonatal sepsis in Africa and South Asia: A meta-analysis of genome-predicted serotype prevalence to inform potential vaccine coverage

Allan Zuza, S. Amin, Jonathan Strysko, Thomas D. Stanton et al.
1 citations
PLoS Medicine
Neonatal and Maternal Infections
41.85
article

Distribution of capsule and O types in Klebsiella pneumoniae causing neonatal sepsis in Africa and South Asia: A meta-analysis of genome-predicted serotype prevalence to inform potential vaccine coverage

Allan Zuza, S. Amin, Jonathan Strysko, Thomas D. Stanton, Oliver Pearse, Alexander M. Aiken, David Ojok, Steven M. Jones, Paul J. Planet, Caroline Tigoi, Aniqa Abdul Rasool, Joveria Farooqi, Kelly L. Wyres, Boaz Wadugu, Chileshe Lukwesa Musyani, Eva Heinz, John Tembo, Wilson Gumbi, Samiah Kanwar, Ahmed M. Moustafa, Kyle Bittinger, Laura Phillips, Rindidzani E. Magobo, Carolyn McGann, Donwilliams O. Omuoyo, Davidson H. Hamer, Kirsty Sands, Varsha Mittal, Ruchi Nanavati, J. W. Cornick, K. K. Jain, Erin Theiller, Shaun P Keegan, Moreka L Ndumba, Atul Jindal, Timothy R. Walsh, Apurba Sastry, Noah Obeng-Nkrumah, Samir K. Saha, Adhisivam Bethou, James C.L. Mwansa, Weiming Hu, Angela Dramowski, Sombo Fwoloshi, Senjuti Saha, M. Jeeva Sankar, Appiah-Korang Labi, Sulagna Basu, Courtney P. Olwagen, Furqan Kabir, Muhammad Imran Nisar, Nicholas A. Feasey, Nelesh P. Govender, Najia Ghanchi, Kathryn E. Holt, Naveed Iqbal, Yogesh Hooda, Semaria Solomon Alemayehu, Susan E. Coffin, Erkison E. Odih, Andrew C. Whitelaw, Erum Khan, Rabaab Zahra, Anudita Bhargava, Anne V. Amulele, James A. Berkley, Patrick Musicha, Arif M. Tanmoy, Jean-Baptiste Mazarati, Shabir A. Madhi, Priyanka S. Prasad, Tolbert Sonda, Matthew T Bates, Waqasuddin Khan, Lola Madrid, Aneeta Hotwani, Fyezah Jehan, Charlene M. C. Rodrigues, Grace J. Chan, Jabir A. Abdulahi, Ramesh K. Agarwal
article en
1 citations

Abstract

Neonatal sepsis is associated with diverse K and O types, with substantial geographic and temporal variation even after adjusting for localised transmission clusters. Despite this, a single 20-valent K vaccine could theoretically cover ≥70% of infections in all target regions. Locally-targeted vaccines could achieve higher coverage with lower valency, but are less feasible. In principle, very high coverage could be achieved with lower valency O-based vaccines, however, the protective efficacy against disease of antibodies targeting the O antigen remains uncertain. Further research is needed on cross-reactivity, antigen exposure, and stability of antigens over time, to better inform vaccine development.

PLoS MedicineVol. 23(1)
Human Sciences Research Council (ZA), National Health Laboratory Service (ZA), South African Medical Research Council (ZA), Boston University (US), Aga Khan University (PK), Quaid-i-Azam University (PK), Centre for Infectious Disease Research in Zambia (ZM), All India Institute of Medical Sciences Raipur (IN), National Security Agency (US), Western Cape Department of Health (ZA), Children's Hospital of Philadelphia (US), Ministry of Health (ZM), University of Ghana (GH), Balochistan University of Information Technology, Engineering and Management Sciences (PK), University of Liverpool (GB), Imperial College Healthcare NHS Trust (GB), Haramaya University (ET), University of Botswana (BW), University of St Andrews (GB), University of Strathclyde (GB), University of the Witwatersrand (ZA), King Edward Memorial Hospital and Seth G.S. Medical College (IN), Liverpool School of Tropical Medicine (GB), Trinity College Dublin (IE), University of Health and Allied Sciences (GH), Stellenbosch University (ZA), Malawi-Liverpool-Wellcome Trust Clinical Research Programme (MW), Wellcome Sanger Institute (GB), University Teaching Hospital (ZM), Tygerberg Hospital (ZA), Kenya Medical Research Institute (KE), Lusaka Apex Medical University (ZM), University of Zambia (ZM), University of Oxford (GB), London School of Hygiene & Tropical Medicine (GB), National Hospital Abuja (NG), Golden Valley Agricultural Research Trust (ZM), INES-Ruhengeri (RW), Kilimanjaro Christian Medical Centre (TZ), National Institute of Research in Tuberculosis (IN), Pamoja Tunaweza Women's Centre (TZ), Child Health Research Foundation (BD), Center for Genomic Science (IT), St. James's Hospital (IE), St. Paul's Hospital Millennium Medical College (ET), National Institute of Public Administration (ZM), National Institute for Communicable Diseases, Kamuzu University of Health Sciences (MW), University of Lincoln (GB), Monash University (AU), Jawaharlal Institute of Post Graduate Medical Education and Research (IN), All India Institute of Medical Sciences (IN), Cardiff University (GB), University of Pennsylvania (US), University of Abuja (NG)
Good health and well-being
Openalex Percentile: Top 2%
Neonatal and Maternal Infections
41.85
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