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Molecular investigation of an outbreak associated with total parenteral nutrition contaminated with NDM-producing Leclercia adecarboxylata

BACKGROUND: This study aimed to determine the epidemiological, microbiological, and molecular characteristics of an outbreak of carbapenem-resistant Leclercia adecarboxylata in three hospitals associated with the unintended use of contaminated total parental nutrition (TPN). METHODS: For 10 days, 25...

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Detalles Bibliográficos
Autores principales: Garza-González, Elvira, Bocanegra-Ibarias, Paola, Rodríguez-Noriega, Eduardo, González-Díaz, Esteban, Silva-Sanchez, Jesús, Garza-Ramos, Ulises, Contreras-Coronado-Tovar, Iván Fernando, Santos-Hernández, José Ecil, Gutiérrez-Bañuelos, David, Mena-Ramirez, Juan Pablo, Ramírez-De-los-Santos, Saúl, Camacho-Ortiz, Adrián, Morfín-Otero, Rayo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916303/
https://www.ncbi.nlm.nih.gov/pubmed/33639886
http://dx.doi.org/10.1186/s12879-021-05923-0
Descripción
Sumario:BACKGROUND: This study aimed to determine the epidemiological, microbiological, and molecular characteristics of an outbreak of carbapenem-resistant Leclercia adecarboxylata in three hospitals associated with the unintended use of contaminated total parental nutrition (TPN). METHODS: For 10 days, 25 patients who received intravenous TPN from the same batch of a formula developed sepsis and had blood cultures positive for L. adecarboxylata. Antimicrobial susceptibility and carbapenemase production were performed in 31 isolates, including one from an unopened bottle of TPN. Carbapenemase-encoding genes, extended-spectrum β-lactamase–encoding genes were screened by PCR, and plasmid profiles were determined. Horizontal transfer of carbapenem resistance was performed by solid mating. Clonal diversity was performed by pulsed-field gel electrophoresis. The resistome was explored by whole-genome sequencing on two selected strains, and comparative genomics was performed using Roary. RESULTS: All 31 isolates were resistant to aztreonam, cephalosporins, carbapenems, trimethoprim/sulfamethoxazole, and susceptible to gentamicin, tetracycline, and colistin. Lower susceptibility to levofloxacin (51.6%) and ciprofloxacin (22.6%) was observed. All the isolates were carbapenemase producers and positive for bla(NDM-1), bla(TEM-1B), and bla(SHV-12) genes. One main lineage was detected (clone A, 83.9%; A1, 12.9%; A2, 3.2%). The bla(NDM-1) gene is embedded in a Tn125-like element. Genome analysis showed genes encoding resistance for aminoglycosides, quinolones, trimethoprim, colistin, phenicols, and sulphonamides and the presence of IncFII (Yp), IncHI2, and IncHI2A incompatibility groups. Comparative genomics showed a major phylogenetic relationship among L. adecarboxylata I1 and USDA-ARS-USMARC-60222 genomes, followed by our two selected strains. CONCLUSION: We present epidemiological, microbiological, and molecular evidence of an outbreak of carbapenem-resistant L. adecarboxylata in three hospitals in western Mexico associated with the use of contaminated TPN. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-021-05923-0.