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  4. A multispecies outbreak of carbapenem-resistant bacteria harboring the blaKPC gene in a non-classical transposon element
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A multispecies outbreak of carbapenem-resistant bacteria harboring the blaKPC gene in a non-classical transposon element

Journal
BMC Microbiology
ISSN
1471-2180
Date Issued
2021
Author(s)
Aniela Wozniak
Cristian Figueroa
Francisco Moya-Flores
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Piero Guggiana
Claudia Castillo
RIVAS JIMENEZ, LINA MARIA  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Patricia C. García
MUNITA SEPULVEDA, JOSE MANUEL  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85104158445
WoS ID
WOS:000639121700001
DOI
10.1186/s12866-021-02169-3
URL
https://investigadores.udd.cl/handle/123456789/5786
URL Institutional Repository
http://hdl.handle.net/11447/5429
Abstract
<jats:title>Abstract</jats:title><jats:sec>
<jats:title>Background</jats:title>
<jats:p><jats:italic>Klebsiella pneumoniae</jats:italic> is the most frequent KPC-producing bacteria. The <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene is frequently embedded in Tn4401 transposon, and less frequently in non-Tn4401 elements (NTE<jats:sub>KPC</jats:sub>) variants I-III. The first case of KPC in the UC-CHRISTUS Clinical Hospital was detected in <jats:italic>Pseudomonas aeruginosa</jats:italic>. Soon after this event, KPC was detected in 2 additional <jats:italic>Pseudomonas aeruginosa</jats:italic>, 3 <jats:italic>Escherichia coli</jats:italic>, 3 <jats:italic>Enterobacter cloacae</jats:italic>, 3 <jats:italic>Klebsiella pneumoniae,</jats:italic> and 1 <jats:italic>Citrobacter freundii</jats:italic>, isolated from 6 different patients. We aimed to elucidate the possible mechanisms of genetic transfer and dissemination of the <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene among isolates of this multispecies outbreak. A molecular epidemiology analysis of the above mentioned clinical isolates (<jats:italic>n</jats:italic> = 13) through Multi-Locus Sequence Typing, plasmid analysis, Pulsed-Field Gel-Electrophoresis, and Whole-genome sequencing (WGS) was performed.</jats:p>
</jats:sec><jats:sec>
<jats:title>Results</jats:title>
<jats:p>High-risk sequence types were found: <jats:italic>K. pneumoniae</jats:italic> ST11, <jats:italic>P. aeruginosa</jats:italic> ST654, and <jats:italic>E. cloacae</jats:italic> ST114. All enterobacterial isolates were not clonal except for 3 <jats:italic>E. coli</jats:italic> isolated from the same patient. WGS analysis in 6 enterobacterial isolates showed that 4 of them had <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> embedded in a novel variant of NTE<jats:sub>KPC</jats:sub> designated NTE<jats:sub>KPC</jats:sub>-IIe. Upstream of <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene there was a 570 pb truncated <jats:italic>bla</jats:italic><jats:sub>TEM-1</jats:sub> gene followed by an insertion sequence that was 84% similar to ISEc63, a 4473 bp element of the Tn3 family. Downstream the <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene there was a truncated ISKpn6 gene, and the inverted repeat right sequence of Tn4401. The ISec63-like element together with the <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene plus Tn4401 remnants were inserted in the Tra operon involved in conjugative transfer of the plasmid. This NTE was carried in a broad host-range IncN plasmid. <jats:italic>P. aeruginosa</jats:italic> isolates carried <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> gene embedded in a typical Tn4401b transposon in a different plasmid, suggesting that there was no plasmid transfer between <jats:italic>Enterobacteriaceae</jats:italic> and <jats:italic>P. aeruginosa</jats:italic> as initially hypothesized.</jats:p>
</jats:sec><jats:sec>
<jats:title>Conclusions</jats:title>
<jats:p>Most enterobacterial isolates had <jats:italic>bla</jats:italic><jats:sub>KPC</jats:sub> embedded in the same NTE<jats:sub>KPC</jats:sub>-IIe element, suggesting that this multispecies KPC outbreak was due to horizontal gene transfer rather than clonal spread. This poses a greater challenge to infection control measures often directed against containment of clonal spread.</jats:p>
</jats:sec>
Subjects
kpc carbapenemase

; 

carbapenem resistant enterobacteriaceae

; 

multispecies outbreak

; 

horizontal gene transfer

; 

bacteria

; 

bacterial infections

; 

beta-lactamases

; 

carbapenem-resistant enterobacteriaceae

; 

carbapenems

; 

disease outbreaks

; 

dna transposable elements

; 

gene transfer, horizontal

; 

humans

; 

pseudomonas aeruginosa

; 

carbapenem

; 

beta lactamase

; 

carbapenem derivative

; 

article

; 

carbapenem resistant klebsiella pneumoniae

; 

carbapenem resistant pseudomonas aeruginosa

; 

carbapenem-resistant enterobacteriaceae

; 

citrobacter freundii

; 

controlled study

; 

enterobacter cloacae

; 

escherichia coli

; 

gene insertion sequence

; 

gene transfer

; 

genetic variation

; 

host range

; 

infection control

; 

klebsiella pneumoniae

; 

molecular epidemiology

; 

multilocus sequence typing

; 

nonhuman

; 

operon

; 

plasmid

; 

pulsed field gel electrophoresis

; 

transposon

; 

whole genome sequencing

; 

bacterial infection

; 

bacterium

; 

drug effect

; 

epidemic

; 

genetics

; 

horizontal gene transfer

; 

human

; 

microbiology

; 

pseudomonas aeruginosa

; 

transposon
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