Clones de alto risco de Klebsiella pneumoniae produtores de ESBL colonizando pacientes de UTI em Natal, Nordeste do Brasil
DOI:
https://doi.org/10.17058/reci.v13i3.18307Palavras-chave:
Klebsiella pneumoniae, Unidade de Tratamento Intensivo, Controle de infecção, Resistência à droga, Beta-lactamasesResumo
Justificativa e objetivos: a colonização por Klebsiella pneumoniae produtora de β-lactamase de espectro estendido (ESBL) em pacientes de Unidade de Terapia Intensiva (UTI) é considerada um fator de risco para infecções, e representa uma fonte de disseminação dessas cepas em instalações hospitalares. Este estudo objetivou realizar a caracterização genética de isolados de K. pneumoniae produtores de ESBL recuperados de swabs de vigilância em uma UTI no Nordeste do Brasil. Métodos: os isolados foram recuperados entre 2018-2019 dos sítios nasal, axilar e retal de 24 pacientes internados na UTI. A identificação bacteriana foi realizada por testes bioquímicos tradicionais. A suscetibilidade antimicrobiana foi avaliada por disco-difusão, e o fenótipo ESBL foi detectado pelo teste de sinergia de duplo-disco. Polymerase chain reaction (PCR) para os genes blaCTX-M, blaSHV e blaTEM, PFGE e MLST foram realizados em isolados representativos. Resultados: foram recuperados 27 isolados de 18 pacientes (75%). A produção de ESBL foi detectada em 85% dos isolados. A resistência à ciprofloxacina, sulfametoxazol/trimetoprima e à maioria dos β-lactâmicos testados foi recorrente, exceto para os carbapenêmicos. Os genes blaSHV, blaTEM e blaCTX-M foram encontrados em alta frequência, e os grupos CTX-M-(1, 2 e 9) foram identificados. Sete sequence types (ST11, ST14, ST17, ST395, ST709, ST855 e ST3827) foram descritos, a maioria deles considerados de alto risco. Conclusão: esses achados enfatizam a ameaça potencial de clones de alto risco bem estabelecidos em uma UTI, e destacam a importância do monitoramento desses clones para prevenir infecções.
Downloads
Referências
Martin RM, Cao J, Brisse S, et al. Molecular Epidemiology of Colonizing and Infecting Isolates of Klebsiella pneumoniae. mSphere. 2016;19;1(5):e00261-16. https://doi.org/10.1128/mSphere.00261-16
Vock I, Tschudin-Sutter S. Persisting intrahospital transmission of multidrug-resistant Klebsiella pneumoniae and challenges for infection control. Infect Control Hosp Epidemiol, 2019;40(8):904-9. https://doi.org/10.1017/ice.2019.153
Agência Nacional de Vigilância Sanitária – ANVISA. Boletim Segurança do Paciente e Qualidade em Serviços de Saúde. nº 23 - Avaliação Nacional dos indicadores de IRAS e RM – 2020, https://www.gov.br/anvisa/pt-br/centraisdeconteudo/publicacoes/servicosdesaude/publicacoes; 2020 [accessed 16 March 2022].
Viale P, Giannella M, Lewis R, et al. Predictors of mortality in multidrug-resistant Klebsiella pneumoniae bloodstream infections. Expert Rev Anti Infect Ther. 2013;11(10):1053-63. https://doi.org/10.1586/14787210.2013.836057
Karlowsky JA, Lob SH, DeRyke CA, et al. Prevalence of ESBL non-CRE Escherichia coli and Klebsiella pneumoniae among clinical isolates collected by the SMART global surveillance programme from 2015 to 2019. Int J Antimicrob Agents. 2022;59(3):106535. https://doi.org/10.1016/j.ijantimicag.2022.106535
Gorrie CL, Mirceta M, Wick RR, et al. Gastrointestinal Carriage Is a Major Reservoir of Klebsiella pneumoniae Infection in Intensive Care Patients. Clin Infect Dis. 2017;15;65(2):208-15. https://doi.org/10.1093/cid/cix270
Navon-Venezia S, Kondratyeva K, Carattoli A. Klebsiella pneumoniae: a major worldwide source and shuttle for antibiotic resistance. FEMS Microbiol Rev. 2017;41(3):252-75. https://doi.org/10.1093/femsre/fux013
Dorman MJ, Short FL. Genome watch: Klebsiella pneumoniae: when a colonizer turns bad. Nat Rev Microbiol. 2017;15(7):384. https://doi.org/10.1038/nrmicro.2017.64
BRASIL. Agência Nacional de Vigilância Sanitária - ANVISA. Microbiologia Clínica para o Controle de Infecção Relacionada à Assistência à Saúde. Módulo 6: Detecção e identificação de bactérias de importância médica Brasília: 1. ed. Brasília: ANVISA; 2010.
Clinical and Laboratory Standards Institute (CLSI): Performance Standards for antimicrobial susceptibility testing; thirtieth informational supplement. CLSI document M100-S30. Wayne, PA.
Clinical and Laboratory Standards Institute (CLSI): Performance Standards for antimicrobial susceptibility testing; twenty-sixth informational supplement. CLSI document M100-S26. Wayne, PA.
Edelstein M, Pimkin M, Palagin I, et al. Prevalence and molecular epidemiology of CTX-M extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae in Russian hospitals. Antimicrob Agents Chemother. 2003;47(12):3724-32. https://doi.org/10.1128/AAC.47.12.3724-3732.2003
Minarini LA, Gales AC, Palazzo IC, et al. Prevalence of community-occurring extended spectrum beta-lactamase-producing Enterobacteriaceae in Brazil. Curr Microbiol. 2007;54(5):335-41. https://doi.org/10.1007/s00284-006-0307-z
Reich F, Atanassova V, Klein G. Extended-spectrum β-lactamase- and AmpC-producing enterobacteria in healthy broiler chickens, Germany. Emerg Infect Dis. 2013;19(8):1253-9. https://doi.org/10.3201/eid1908.120879
Hansen DS, Skov R, Benedí JV, et al. Klebsiella typing: pulsed-field gel electrophoresis (PFGE) in comparison with O:K-serotyping. Clin Microbiol Infect. 2002;8(7):397-404. https://doi:10.1046/j.1469-0691.2002.00411.x
Heras J, Domínguez C, Mata E, et al. GelJ--a tool for analyzing DNA fingerprint gel images. BMC Bioinformatics. 2015;26;16:270. https://doi.org/10.1186/s12859-015-0703-0
Aires CAM, Pereira PS, Rocha-de-Souza CM, et al. Population Structure of KPC-2-Producing Klebsiella pneumoniae Isolated from Surveillance Rectal Swabs in Brazil. Microb Drug Resist. 2020;26(6):652-60. https://doi.org/10.1089/mdr.2019.0166
Ebrahimi F, Mózes J, Monostori J, et al. Comparison of rates of fecal colonization with extended-spectrum beta-lactamase-producing enterobacteria among patients in different wards, outpatients and medical students. Microbiol Immunol. 2016;60(5):285-94. https://doi.org/10.1111/1348-0421.12373
Calfee D, Jenkins SG. Use of active surveillance cultures to detect asymptomatic colonization with carbapenem-resistant Klebsiella pneumoniae in intensive care unit patients. Infect Control Hosp Epidemiol. 2008;29(10):966-8. https://doi.org/10.1086/590661
Maroncle N, Rich C, Forestier C. The role of Klebsiella pneumoniae urease in intestinal colonization and resistance to gastrointestinal stress. Res Microbiol. 2006;157(2):184-93. https://doi.org/10.1016/j.resmic.2005.06.006
Robberts FJ, Kohner PC, Patel R. Unreliable extended-spectrum beta-lactamase detection in the presence of plasmid-mediated AmpC in Escherichia coli clinical isolates. J Clin Microbiol. 2009;47(2):358-61. https://doi.org/10.1128/JCM.01687-08
Zahar JR, Blot S, Nordmann P, et al. Screening for Intestinal Carriage of Extended-spectrum Beta-lactamase-producing Enterobacteriaceae in Critically Ill Patients: Expected Benefits and Evidence-based Controversies. Clin Infect Dis. 2019;30;68(12):2125-30. https://doi.org/10.1093/cid/ciy864
Castanheira M, Simner PJ, Bradford PA. Extended-spectrum β-lactamases: an update on their characteristics, epidemiology and detection. JAC Antimicrob Resist. 2021;16;3(3):dlab092. https://doi.org/10.1093/jacamr/dlab092
Sánchez-López J, Cantón R. Current status of ESKAPE microorganisms in Spain: Epidemiology and resistance phenotypes. Rev Esp Quimioter. 2019;32 Suppl 2(Suppl 2):27-31.
Lee AHY, Porto WF, de Faria C Jr, et al. Genomic insights into the diversity, virulence and resistance of Klebsiella pneumoniae extensively drug resistant clinical isolates. Microb Genom. 2021;7(8):000613. https://doi.org/10.1099/mgen.0.000613
Rodrigues YC, Lobato ARF, Quaresma AJPG, et al. The Spread of NDM-1 and NDM-7-Producing Klebsiella pneumoniae Is Driven by Multiclonal Expansion of High-Risk Clones in Healthcare Institutions in the State of Pará, Brazilian Amazon Region. Antibiotics (Basel). 2021;14;10(12):1527. https://doi.org/10.3390/antibiotics10121527
Rodrigues C, Hauser K, Cahill N, et al. High Prevalence of Klebsiella pneumoniae in European Food Products: a Multicentric Study Comparing Culture and Molecular Detection Methods. Microbiol Spectr. 2022;23;10(1):e0237621. https://doi.org/10.1128/spectrum.02376-21
Cerdeira L, Monte DFM, Fuga B, et al. Genomic insights of Klebsiella pneumoniae isolated from a native Amazonian fish reveal wide resistome against heavy metals, disinfectants, and clinically relevant antibiotics. Genomics. 2020;112(6):5143-46. https://doi.org/10.1016/j.ygeno.2020.09.015
Downloads
Publicado
Como Citar
Edição
Seção
Licença
Copyright (c) 2023 Isabela Maria Fortaleza Neves Bomfim, Marcileide Almeida Amaral, Yan Corrêa Rodrigues, Dra. Danielle Murici Brasiliense, Caio Augusto Martins Aires, Renato Motta Neto
Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.
The author must state that the paper is original (has not been published previously), not infringing any copyright or other ownership right involving third parties. Once the paper is submitted, the Journal reserves the right to make normative changes, such as spelling and grammar, in order to maintain the language standard, but respecting the author’s style. The published papers become ownership of RECI, considering that all the opinions expressed by the authors are their responsibility. Because we are an open access journal, we allow free use of articles in educational and scientific applications provided the source is cited under the Creative Commons CC-BY license.