Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.

OBJECTIVES:ESBL-producing Klebsiella pneumoniae (KPN) pose a major threat to human health globally. We carried out a WGS study to understand the genetic background of ESBL-producing KPN in Malawi and place them in the context of other global isolates. METHODS:We sequenced genomes of 72 invasive and...

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मुख्य लेखकों: Musicha, P, Msefula, C, Mather, A, Chaguza, C, Cain, A, Peno, C, Kallonen, T, Khonga, M, Denis, B, Gray, K, Heyderman, R, Thomson, N, Everett, D, Feasey, N
स्वरूप: Journal article
भाषा:English
प्रकाशित: Oxford University Press 2019
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author Musicha, P
Msefula, C
Mather, A
Chaguza, C
Cain, A
Peno, C
Kallonen, T
Khonga, M
Denis, B
Gray, K
Heyderman, R
Thomson, N
Everett, D
Feasey, N
author_facet Musicha, P
Msefula, C
Mather, A
Chaguza, C
Cain, A
Peno, C
Kallonen, T
Khonga, M
Denis, B
Gray, K
Heyderman, R
Thomson, N
Everett, D
Feasey, N
author_sort Musicha, P
collection OXFORD
description OBJECTIVES:ESBL-producing Klebsiella pneumoniae (KPN) pose a major threat to human health globally. We carried out a WGS study to understand the genetic background of ESBL-producing KPN in Malawi and place them in the context of other global isolates. METHODS:We sequenced genomes of 72 invasive and carriage KPN isolates collected from patients admitted to Queen Elizabeth Central Hospital, Blantyre, Malawi. We performed phylogenetic and population structure analyses on these and previously published genomes from Kenya (n = 66) and from outside sub-Saharan Africa (n = 67). We screened for presence of antimicrobial resistance (AMR) genetic determinants and carried out association analyses by genomic sequence cluster, AMR phenotype and time. RESULTS:Malawian isolates fit within the global population structure of KPN, clustering into the major lineages of KpI, KpII and KpIII. KpI isolates from Malawi were more related to those from Kenya, with both collections exhibiting more clonality than isolates from the rest of the world. We identified multiple ESBL genes, including blaCTX-M-15, several blaSHV, blaTEM-63 and blaOXA-10, and other AMR genes, across diverse lineages of the KPN isolates from Malawi. No carbapenem resistance genes were detected; however, we detected IncFII and IncFIB plasmids that were similar to the carbapenem resistance-associated plasmid pNDM-mar. CONCLUSIONS:There are multiple ESBL genes across diverse KPN lineages in Malawi and plasmids in circulation that are capable of carrying carbapenem resistance. Unless appropriate interventions are rapidly put in place, these may lead to a high burden of locally untreatable infection in vulnerable populations.
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spelling oxford-uuid:a2a322ac-57f5-438a-9189-2b44016644182022-03-27T02:21:23ZGenomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a2a322ac-57f5-438a-9189-2b4401664418EnglishSymplectic Elements at OxfordOxford University Press2019Musicha, PMsefula, CMather, AChaguza, CCain, APeno, CKallonen, TKhonga, MDenis, BGray, KHeyderman, RThomson, NEverett, DFeasey, NOBJECTIVES:ESBL-producing Klebsiella pneumoniae (KPN) pose a major threat to human health globally. We carried out a WGS study to understand the genetic background of ESBL-producing KPN in Malawi and place them in the context of other global isolates. METHODS:We sequenced genomes of 72 invasive and carriage KPN isolates collected from patients admitted to Queen Elizabeth Central Hospital, Blantyre, Malawi. We performed phylogenetic and population structure analyses on these and previously published genomes from Kenya (n = 66) and from outside sub-Saharan Africa (n = 67). We screened for presence of antimicrobial resistance (AMR) genetic determinants and carried out association analyses by genomic sequence cluster, AMR phenotype and time. RESULTS:Malawian isolates fit within the global population structure of KPN, clustering into the major lineages of KpI, KpII and KpIII. KpI isolates from Malawi were more related to those from Kenya, with both collections exhibiting more clonality than isolates from the rest of the world. We identified multiple ESBL genes, including blaCTX-M-15, several blaSHV, blaTEM-63 and blaOXA-10, and other AMR genes, across diverse lineages of the KPN isolates from Malawi. No carbapenem resistance genes were detected; however, we detected IncFII and IncFIB plasmids that were similar to the carbapenem resistance-associated plasmid pNDM-mar. CONCLUSIONS:There are multiple ESBL genes across diverse KPN lineages in Malawi and plasmids in circulation that are capable of carrying carbapenem resistance. Unless appropriate interventions are rapidly put in place, these may lead to a high burden of locally untreatable infection in vulnerable populations.
spellingShingle Musicha, P
Msefula, C
Mather, A
Chaguza, C
Cain, A
Peno, C
Kallonen, T
Khonga, M
Denis, B
Gray, K
Heyderman, R
Thomson, N
Everett, D
Feasey, N
Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title_full Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title_fullStr Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title_full_unstemmed Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title_short Genomic analysis of Klebsiella pneumoniae isolates from Malawi reveals acquisition of multiple ESBL determinants across diverse lineages.
title_sort genomic analysis of klebsiella pneumoniae isolates from malawi reveals acquisition of multiple esbl determinants across diverse lineages
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