Rectal Carriage of Sequence Type 307 <i>Klebsiella pneumoniae</i> High‐Risk Clone Harboring Multiple Carbapenemase Genes in Community Hospitals Gauteng, South Africa
Asymptomatic rectal carriers are recognized as reservoirs of carbapenem-resistant Klebsiella pneumoniae (CRKp), which can spread epidemic high-risk clones [e.g., sequence types (ST)-307] and plasmids [incompatibility group (Inc)-X3] in hospitals, with possible transmission into the community. This study investigated the epidemiology and characteristics of CRKp high-risk clones ST307 among rectal carriage isolates from community hospitals. A carbapenemase positivity rate of 24% was observed for all rectal screening performed during hospital admission (February to August 2021) in Gauteng, South Africa; 252 CRKp isolates were characterized. Antimicrobial susceptibility was performed using the VITEK 2 automated system, and polymerase chain reaction assays were used to detect K. pneumoniae ST307, carbapenemase genes, and associated mobile genetic elements (MGEs e.g., IncX3, IS3000). Of the 252 isolates, 25% (64/252) were ST307 positive and 75% (188/252) were non-ST307. Among the 64 ST307, 45% (29/64) harbored bla<sub>OXA-181</sub> on IncX3 plasmids. Occurrence of bla<sub>OXA-181</sub> among ST307 (69%; 44/64) when compared to non-ST307 (48%; 91/188) was statistically significant (p-value = 0.002). Fourteen isolates, including two ST307, harbored double carbapenemase genes. Carbapenemase gene combinations include six bla<sub>NDM</sub>+bla<sub>OXA-48-like</sub>, four bla<sub>NDM</sub> +bla<sub>OXA-181</sub>, three bla<sub>KPC</sub>+bla<sub>OXA-181</sub>, and one bla<sub>OXA-181</sub>+bla<sub>VIM</sub>. One ST307 isolate harbored three carbapenemase genes (bla<sub>NDM</sub>+bla<sub>OXA-48</sub>+bla<sub>OXA-181</sub>). Level of antimicrobial resistance was significantly (p-value < 0.001) associated with the occurrence of ST307, comprising 73% (47/64) extensively drug resistant. This study highlights the need for rectal screening of XDR clones and plasmids using simple and cost-effective genomic methodologies suitable for low- and middle-income countries for local risk management and control of infectious diseases in hospitals.
Authors
- Marthie M. Ehlers (ORCID: https://orcid.org/0000-0003-2199-6970)
- Kathy‐Anne Strydom (ORCID: https://orcid.org/0000-0003-0771-8608)
- Chanel Kingsburgh (ORCID: https://orcid.org/0000-0003-1493-1554)
- Marleen M. Kock (ORCID: https://orcid.org/0000-0002-1768-9268)
- Kafilat Taiwo Salvador‐Oke (ORCID: https://orcid.org/0000-0003-1049-596X)
- Gisele Peirano
- Johann D D Pitout (ORCID: https://orcid.org/0000-0002-4547-4707)
Institutions
- National Health Laboratory Service (ZA)
- University of Calgary (CA)
- Education Labour Relations Council (ZA)
- MD Precision (Canada) (CA)
- University of Pretoria (ZA)
Publication Details
- Journal
- MicrobiologyOpen
- Published
- 2025-11-14
- DOI
- https://doi.org/10.1002/mbo3.70152
- Primary Topic
- Antibiotic Resistance in Bacteria
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Research Foundation
- University of Pretoria
- National Health Laboratory Service