Pathogenomics and evolutionary epidemiology of multi-drug resistant clinical Klebsiella pneumoniae isolated from Pretoria, South Africa

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dc.contributor.author Mbelle, Nontombi Marylucy
dc.contributor.author Feldman, Charles
dc.contributor.author Osei Sekyere, John
dc.contributor.author Maningi, Nontuthuko Excellent
dc.contributor.author Modipane, Lesedi
dc.contributor.author Essack, Sabiha Yusuf
dc.date.accessioned 2021-04-08T11:42:41Z
dc.date.available 2021-04-08T11:42:41Z
dc.date.issued 2020
dc.description Part of this work was presented at the International Society for Infectious Diseases (ISID) Congress, Buenos Aires, Argentina, 2018 (Abstract #1732) and the American Society of Microbiology (ASM) congress, Atlanta, USA 2018 (Abstract #5351). en_ZA
dc.description Supplementary information: Supplementary Table S1. Supplementary Table S2. Supplementary Data S3. Supplementary Data S4. en_ZA
dc.description.abstract Antibiotic-resistant Klebsiella pneumoniae is increasingly being implicated in invasive infections worldwide with high mortalities. Forty-two multidrug resistant (MDR) K. pneumoniae isolates were collected over a 4-month period. Antimicrobial susceptibility was determined using Microscan. The evolutionary epidemiology, resistome, virulome and mobilome of the isolates were characterised using whole-genome sequencing and bioinformatics analysis. All isolates contained the blaCTX-M gene, whilst 41/42(97%) contained blaTEM, 36/42(86%) contained blaOXA and 35/42(83%) harboured blaSHV genes. Other resistance genes found included blaLEN, aac(6′)-lb-cr, qnrA, qnrB, qnrS, oqxAB, aad, aph, dfr, sul1, sul2, fosA, and cat genes. Fluoroquinolone and colistin resistance-conferring mutations in parC, gyrAB, pmrAB, phoPQ and kpnEF were identified. The blaLEN gene, rarely described worldwide, was identified in four isolates. The isolates comprised diverse sequence types, the most common being ST152 in 7/42(17%) isolates; clone-specific O and K capsule types were identified. Diverse virulence genes that were not clone-specific were identified in all but one isolate. IncF, IncH and IncI plasmid replicons and two novel integrons were present. The blaCTX-M-15 and blaTEM-1 genes were bracketed by Tn3 transposons, ISEc9, a resolvase and IS91 insertion sequence. There were 20 gene cassettes in 14 different cassette arrays, with the dfrA and aadA gene cassettes being the most frequent. Phylogenetic analysis demonstrated that the isolates were evolutionarily associated with strains from both South Africa and abroad. These findings depict the rich resistome, mobilome and virulome repertoire in clinical K. pneumoniae strains, which are mainly transmitted by clonal, multiclonal and horizontal means in South Africa. en_ZA
dc.description.department Medical Microbiology en_ZA
dc.description.librarian am2021 en_ZA
dc.description.sponsorship The National Health Laboratories Services, the University of Pretoria and the South African Medical Research Council. en_ZA
dc.description.uri http://www.nature.com/srep en_ZA
dc.identifier.citation Mbelle, N.M., Feldman, C., Osei Sekyere, J. et al. 2020, 'Pathogenomics and evolutionary epidemiology of multi-drug resistant clinical Klebsiella pneumoniae isolated from Pretoria, South Africa', Scientific Reports, vol. 10, art. 1232, pp. 1-17. en_ZA
dc.identifier.issn 2045-2322 (online)
dc.identifier.other 10.1038/s41598-020-58012-8
dc.identifier.uri http://hdl.handle.net/2263/79361
dc.language.iso en en_ZA
dc.publisher Nature Publishing Group en_ZA
dc.rights © The Author(s) 2020. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License. en_ZA
dc.subject Antimicrobial susceptibility en_ZA
dc.subject Microscan en_ZA
dc.subject Multidrug resistant (MDR) en_ZA
dc.subject Antibiotic resistance en_ZA
dc.title Pathogenomics and evolutionary epidemiology of multi-drug resistant clinical Klebsiella pneumoniae isolated from Pretoria, South Africa en_ZA
dc.type Article en_ZA


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