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Clones and Clusters of Antimicrobial-Resistant Klebsiella from Southwestern Nigeria
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ABSTRACT
Introduction
Klebsiella pneumoniae
is a World Health Organization high-priority antibiotic-resistant pathogen. However, little is known about the population structure and evolution of
Klebsiella
circulating in Nigeria.
Methods
We performed whole genome sequencing (WGS) of 141
Klebsiella
isolated between 2016 and 2018 from clinical specimens at 3 antimicrobial-resistance (AMR) sentinel surveillance tertiary hospitals in southwestern Nigeria. We conducted
in silico
multilocus sequence typing, AMR gene, virulence gene, plasmid, and K and O loci profiling, as well as phylogenetic analyses, using publicly available tools and Nextflow pipelines.
Results
Phylogenetic analysis revealed that the majority of the 134
K. pneumoniae
and 5
K. quasipneumoniae
isolates from Nigeria characterized are closely related to globally disseminated multidrug-resistant clones. Of the 39
K. pneumoniae
sequence types (STs) identified, the most common were ST307 (15%), ST5241 (12%), ST15 (~9%), and ST25 (~6%). ST5241, one of 10 novel STs detected, is a single locus variant of ST636 carrying
dfrA14
,
tetD
,
qnrS
, and
oqxAB
resistance genes. The extended-spectrum β lactamase (ESBL) gene
bla
CTX_M-15 was seen in 72 % of
K. pneumoniae
genomes, while 8% encoded a carbapenemase. Four likely outbreak clusters from one facility, within STs 17, 25, 307, and 5241, were ESBL but not carbapenemase-bearing clones.
Conclusion
This study uncovered known and novel
K. pneumoniae
lineages circulating in Nigeria that include multidrug-resistant ESBL producers. Carbapenemase-producing isolates remain uncommon. WGS retrospectively identified outbreak clusters, pointing to the value of genomic approaches in AMR surveillance for improving infection prevention and control in Nigerian hospitals.
summary
We performed whole genome sequencing (WGS) of 141
Klebsiella
isolated in 2016-2018 at 3 antimicrobial-resistance (AMR) sentinel surveillance tertiary hospitals in southwestern Nigeria. This study uncovered known and novel
K. pneumoniae
lineages circulating in Nigeria that include multidrug-resistant ESBL producers.
FUNDING
This work was supported by Official Development Assistance (ODA) funding from the National Institute of Health Research [16/136/111: NIHR Global Health Research Unit on Genomic Surveillance of Antimicrobial Resistance].
This research was commissioned by the National Institute of Health Research using Official Development Assistance (ODA) funding. INO is an African Research Leader supported by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement that is also part of the EDCTP2 program supported by the European Union. The funders had no role in the content, crafting or submission of this paper. The views expressed in this publication are those of the authors and not necessarily those of the funders or their affiliates.
CONFLICT OF INTEREST
The authors: No reported conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.
openRxiv
Ayorinde O. Afolayan
Anderson O. Oaikhena
Aaron O. Aboderin
Olatunde F. Olabisi
Adewale A. Amupitan
Oyekola V. Abiri
Veronica O. Ogunleye
Anthony Underwood
Erkison Ewomazino Odih
Abolaji T. Adeyemo
Adeyemi T. Adeyemo
Temitope O. Obadare
Sophia David
Silvia Argimón
Monica Abrudan
Abiodun Egwuenu
Chikwe Ihekweazu
David M. Aanensen
Iruka N. Okeke
Title: Clones and Clusters of Antimicrobial-Resistant
Klebsiella
from Southwestern Nigeria
Description:
ABSTRACT
Introduction
Klebsiella pneumoniae
is a World Health Organization high-priority antibiotic-resistant pathogen.
However, little is known about the population structure and evolution of
Klebsiella
circulating in Nigeria.
Methods
We performed whole genome sequencing (WGS) of 141
Klebsiella
isolated between 2016 and 2018 from clinical specimens at 3 antimicrobial-resistance (AMR) sentinel surveillance tertiary hospitals in southwestern Nigeria.
We conducted
in silico
multilocus sequence typing, AMR gene, virulence gene, plasmid, and K and O loci profiling, as well as phylogenetic analyses, using publicly available tools and Nextflow pipelines.
Results
Phylogenetic analysis revealed that the majority of the 134
K.
pneumoniae
and 5
K.
quasipneumoniae
isolates from Nigeria characterized are closely related to globally disseminated multidrug-resistant clones.
Of the 39
K.
pneumoniae
sequence types (STs) identified, the most common were ST307 (15%), ST5241 (12%), ST15 (~9%), and ST25 (~6%).
ST5241, one of 10 novel STs detected, is a single locus variant of ST636 carrying
dfrA14
,
tetD
,
qnrS
, and
oqxAB
resistance genes.
The extended-spectrum β lactamase (ESBL) gene
bla
CTX_M-15 was seen in 72 % of
K.
pneumoniae
genomes, while 8% encoded a carbapenemase.
Four likely outbreak clusters from one facility, within STs 17, 25, 307, and 5241, were ESBL but not carbapenemase-bearing clones.
Conclusion
This study uncovered known and novel
K.
pneumoniae
lineages circulating in Nigeria that include multidrug-resistant ESBL producers.
Carbapenemase-producing isolates remain uncommon.
WGS retrospectively identified outbreak clusters, pointing to the value of genomic approaches in AMR surveillance for improving infection prevention and control in Nigerian hospitals.
summary
We performed whole genome sequencing (WGS) of 141
Klebsiella
isolated in 2016-2018 at 3 antimicrobial-resistance (AMR) sentinel surveillance tertiary hospitals in southwestern Nigeria.
This study uncovered known and novel
K.
pneumoniae
lineages circulating in Nigeria that include multidrug-resistant ESBL producers.
FUNDING
This work was supported by Official Development Assistance (ODA) funding from the National Institute of Health Research [16/136/111: NIHR Global Health Research Unit on Genomic Surveillance of Antimicrobial Resistance].
This research was commissioned by the National Institute of Health Research using Official Development Assistance (ODA) funding.
INO is an African Research Leader supported by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID Concordat agreement that is also part of the EDCTP2 program supported by the European Union.
The funders had no role in the content, crafting or submission of this paper.
The views expressed in this publication are those of the authors and not necessarily those of the funders or their affiliates.
CONFLICT OF INTEREST
The authors: No reported conflicts of interest.
All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest.
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