Genomic analysis of <i>Klebsiella pneumoniae</i> causing community-acquired respiratory deaths among Zambian infants and children using targeted RNA-probe hybridization-capture metagenomics

<i>Klebsiella pneumoniae</i> (Kp) is a leading cause of neonatal and infant deaths in sub-Saharan Africa and frequently associated with antimicrobial resistance. Previously, we identified Kp as a major cause of fatal community-associated lower respiratory infections among infants and children under five years in Lusaka, Zambia, using postmortem tissue sampling and pathogen specific multiplex qPCR. In this follow-up study, we employed a novel culture-independent RNA-probe hybridization-capture metagenomic sequencing approach, targeting Kp pan-genome core and accessory genes, to perform in-depth genomic analysis of Kp from eleven post-mortem lung biopsy samples from seven of these children. Analysis detected Kp in all cases except one, which identified <i>Klebsiella quasipneumoniae</i> subspecies <i>similipneumoniae</i>. Core-genome multi-locus sequence typing (cgMLST) revealed six clonal groups (CG607, CG1123, CG10072, CG280, CG3648, and CG10344) belonging to five sublineages (SL607, SL17, SL280, SL37, and SL10072), with perfect concordance between paired samples from the same case. Two infants sampled the same month harbored SL607 lineages sharing 621 out of 629 cgMLST alleles, suggesting clonal spread. Kp capsule (K) loci were detected in all but one case and included potential vaccine targets KL25, KL23, and KL122. Antimicrobial resistance genes were widespread among samples, particularly encoding resistance toward aminoglycosides, β-lactams, sulphonamides, tetracyclines, and trimethoprim. Extended spectrum β-lactamases were identified in four cases, three of which were <i>bla</i> <sub>CTX-M-15</sub>. The acquired Kp sideophore yersiniabactin (lineage <i>ybt14</i>) was identified in both cases associated with SL607, and the acquired siderophore aerobactin (lineage <i>iuc5</i>) was identified in one of these, suggesting possible convergence of antimicrobial resistance and hypervirulence. The detection of Kp with extensive antimicrobial resistance causing fatal community acquired pneumonia signals a deeply concerning epidemiologic shift from a largely nosocomial pathogen. This calls for urgent epidemiological investigations to better understand the burden, transmission dynamics, antimicrobial resistances, and potential vaccine targets for Kp in other community settings across sub-Saharan Africa.

Authors

Institutions

Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-05
DOI
https://doi.org/10.64898/2026.02.02.703236
Primary Topic
Antibiotic Resistance in Bacteria
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Genomic analysis of Klebsiella pneumoniae causing community-acquired respiratory deaths among Zambian infants and children using targeted RNA-probe hybridization-capture metagenomics

Chilufya Chikoti, Emilia Jumbe Marsden, Mulemba Samutela, Sundsfjord Arnfinn et al.
bioRxiv (Cold Spring Harbor Laboratory)
Antibiotic Resistance in Bacteria
article

Genomic analysis of Klebsiella pneumoniae causing community-acquired respiratory deaths among Zambian infants and children using targeted RNA-probe hybridization-capture metagenomics

Chilufya Chikoti, Emilia Jumbe Marsden, Mulemba Samutela, Sundsfjord Arnfinn, Christopher Gill, Sarah Chirwa, Chibamba Mumba, Lisa Kafula Nkole, Alyse Wheelock, Kenneth Lindstedt, Rachel Pieciak, Diana Nzara, Charles Chimoga, Edgar Simulundu, Bwalya Mulenga, Benard Ngoma, Natasha Namuziya, L. Pemba, Mwelwa Chasaya, Wasifa Kabir, Leah Forman, Kathryn E. Holt, James Thumba Lungu, William MacLeod, Victor Mudenda, Somwe Wa Somwe, Crispin Moyo
article en

Abstract

<i>Klebsiella pneumoniae</i> (Kp) is a leading cause of neonatal and infant deaths in sub-Saharan Africa and frequently associated with antimicrobial resistance. Previously, we identified Kp as a major cause of fatal community-associated lower respiratory infections among infants and children under five years in Lusaka, Zambia, using postmortem tissue sampling and pathogen specific multiplex qPCR. In this follow-up study, we employed a novel culture-independent RNA-probe hybridization-capture metagenomic sequencing approach, targeting Kp pan-genome core and accessory genes, to perform in-depth genomic analysis of Kp from eleven post-mortem lung biopsy samples from seven of these children. Analysis detected Kp in all cases except one, which identified <i>Klebsiella quasipneumoniae</i> subspecies <i>similipneumoniae</i>. Core-genome multi-locus sequence typing (cgMLST) revealed six clonal groups (CG607, CG1123, CG10072, CG280, CG3648, and CG10344) belonging to five sublineages (SL607, SL17, SL280, SL37, and SL10072), with perfect concordance between paired samples from the same case. Two infants sampled the same month harbored SL607 lineages sharing 621 out of 629 cgMLST alleles, suggesting clonal spread. Kp capsule (K) loci were detected in all but one case and included potential vaccine targets KL25, KL23, and KL122. Antimicrobial resistance genes were widespread among samples, particularly encoding resistance toward aminoglycosides, β-lactams, sulphonamides, tetracyclines, and trimethoprim. Extended spectrum β-lactamases were identified in four cases, three of which were <i>bla</i> <sub>CTX-M-15</sub>. The acquired Kp sideophore yersiniabactin (lineage <i>ybt14</i>) was identified in both cases associated with SL607, and the acquired siderophore aerobactin (lineage <i>iuc5</i>) was identified in one of these, suggesting possible convergence of antimicrobial resistance and hypervirulence. The detection of Kp with extensive antimicrobial resistance causing fatal community acquired pneumonia signals a deeply concerning epidemiologic shift from a largely nosocomial pathogen. This calls for urgent epidemiological investigations to better understand the burden, transmission dynamics, antimicrobial resistances, and potential vaccine targets for Kp in other community settings across sub-Saharan Africa.

bioRxiv (Cold Spring Harbor Laboratory)
Boston University (US), University Hospital of North Norway (NO), University Teaching Hospital (ZM), University of Zambia (ZM), Nemours Children’s Clinic (US), London School of Hygiene & Tropical Medicine (GB), Centre for Arctic Gas Hydrate, Environment and Climate (NO), Golden Valley Agricultural Research Trust (ZM), Zambia National Public Health Institute (ZM), National HIV/AIDS/STI/TB Council (ZM), Monash University (AU), UiT The Arctic University of Norway (NO)
Bill and Melinda Gates Foundation, Universitetet i Tromsø, Trond Mohn stiftelse, Monash University, University of Melbourne
Good health and well-being
Openalex Percentile: Top 63%
Antibiotic Resistance in Bacteria
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.