doi: 10.1016/j.meegid.2021.105122.
Online ahead of print.
1
, Humberlânia de Sousa Duarte
1
, Gabriela Bergiante Kraychete
1
, Mayara Gil de Castro Santos
1
, Rossiane Claudia Vommaro
2
, Carla Ormund Gonçalves Ximenes Lima
1
, Daiana Lima-Morales
3
, Priscila Lamb Wink
3
, Eliane de Oliveira Ferreira
1
, Renata Cristina Picão
4
, Vinícius Magno da Rocha
5
Affiliations
Affiliations
- 1 Instituto de Microbiologia Paulo de Góes, Departamento de Microbiologia Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
- 2 Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho e Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagens, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
- 3 Instituto Nacional de Pesquisa em Resistência a Antimicrobianos, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil.
- 4 Instituto de Microbiologia Paulo de Góes, Departamento de Microbiologia Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. Electronic address: [email protected].
- 5 Departamento de Cirurgia Geral e Especializada, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
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Luana Boff et al.
Infect Genet Evol.
.
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doi: 10.1016/j.meegid.2021.105122.
Online ahead of print.
Authors
1
, Humberlânia de Sousa Duarte
1
, Gabriela Bergiante Kraychete
1
, Mayara Gil de Castro Santos
1
, Rossiane Claudia Vommaro
2
, Carla Ormund Gonçalves Ximenes Lima
1
, Daiana Lima-Morales
3
, Priscila Lamb Wink
3
, Eliane de Oliveira Ferreira
1
, Renata Cristina Picão
4
, Vinícius Magno da Rocha
5
Affiliations
- 1 Instituto de Microbiologia Paulo de Góes, Departamento de Microbiologia Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
- 2 Laboratório de Ultraestrutura Celular Hertha Meyer, Instituto de Biofísica Carlos Chagas Filho e Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagens, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
- 3 Instituto Nacional de Pesquisa em Resistência a Antimicrobianos, Hospital de Clínicas de Porto Alegre, Rio Grande do Sul, Brazil.
- 4 Instituto de Microbiologia Paulo de Góes, Departamento de Microbiologia Médica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil. Electronic address: [email protected].
- 5 Departamento de Cirurgia Geral e Especializada, Universidade Federal do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.
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Abstract
Surgical site infections in instrumented posterior lumbar interbody fusion surgery are normally due to gram-positive bacteria, but gram-negative bacteria can cause infections in cases involving lower lumbar interventions as its closer to the perianal area. Here we report an uncommon fatal wound infection caused by a multidrug-resistant Klebsiella pneumoniae after an elective spine surgery. In silico analysis revealed that LWI_ST16 belonged to ST16, an emergent international clone notable for its increased virulence potential. We also observed that this strain carried a conjugative IncF plasmid encoding resistance genes to beta-lactams (blaKPC-2 and blaOXA-1), tetracycline (tetA), aminoglycosides and fluoroquinolones (aac(6′)-Ib-cr). The carbapenemase encoding gene blaKPC-2 was located on a Tn4401e transposon previously characterized to increase blaKPC expression. LWI_ST16 is a strong biofilm producer on polystyrene and capable of forming tower-like structures on a titanium device like the one inserted in the patient’s spine. Our findings strengthen the valuable contribution of continuous surveillance of multidrug-resistant and high-risk K. pneumoniae clones to avoid unfavourable clinical outcomes.
Keywords:
Biofilm; Carbapenemase; High-risk clone; KPC-2; Klebsiella pneumoniae; ST16.
Copyright © 2021. Published by Elsevier B.V.
Conflict of interest statement
Declaration of Competing Interest The authors declare no conflict of interest regarding the publication of this article.
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