Whole-Genome Analysis of Extensively Drug-Resistant Enterobacter hormaechei Isolated from a Patient with Non-Hodgkin’s Lymphoma
Author:
Ferreira Cristina Motta1ORCID, Naveca Felipe Gomes2ORCID, Ferreira Guilherme Motta Antunes3, Barbosa Maria de Nazaré Saunier1, de Souza Victor Costa2, Calheiros Franceline Oliveira1, Souza Vander Silva1, Ferreira William Antunes4
Affiliation:
1. Fundação Hospitalar de Hematologia e Hemoterapia do Amazonas—HEMOAM, Av. Constantino Nery, 4397, Chapada, Manaus 69050-001, Amazonas, Brazil 2. Instituto Leônidas e Maria Deane—FIOCRUZ, Rua Teresina, 476, Adrianópolis, Manaus 69027-070, Amazonas, Brazil 3. Programa de Pós-Graduação em Hematologia, Universidade do Estado do Amazonas—PPGH-UEA/HEMOAM, Av. Constantino Nery, 4397, Chapada, Manaus 69050-001, Amazonas, Brazil 4. Fundação de Dermatologia Tropical e Venereologia Alfredo da Matta—FUAM, Rua Codajás, 24, Cachoeirinha, Manaus 69065-130, Amazonas, Brazil
Abstract
Background: Currently, the Enterobacteriaceae species are responsible for a variety of serious infections and are already considered a global public health problem, especially in underdeveloped countries, where surveillance and monitoring programs are still scarce and limited. Analyses were performed on the complete genome of an extensively antibiotic-resistant strain of Enterobater hormaechei, which was isolated from a patient with non-Hodgkin’s lymphoma, who had been admitted to a hospital in the city of Manaus, Brazil. Methods: Phenotypical identification and susceptibility tests were performed in automated equipment. Total DNA extraction was performed using the PureLink genomic DNA mini-Kit. The genomic DNA library was prepared with Illumina Microbial Amplicon Prep and sequenced in the MiSeq Illumina Platform. The assembly of the whole-genome and individual analyses of specific resistance genes extracted were carried out using online tools and the Geneious Prime software. Results: The analyses identified an extensively resistant ST90 clone of E. hormaechei carrying different genes, including blaCTX-M-15, blaGES-2, blaTEM-1A, blaACT-15, blaOXA-1 and blaNDM-1, [aac(3)-IIa, aac(6′)-Ian, ant(2″)-Ia], [aac(6′)-Ib-cr, (qnrB1)], dfrA25, sul1 and sul2, catB3, fosA, and qnrB, in addition to resistance to chlorhexidine, which is widely used in patient antisepsis. Conclusions: These findings highlight the need for actions to control and monitor these pathogens in the hospital environment.
Funder
Fundação de Amparo à Pesquisa do Estado do Amazonas (FAPEAM)- POSGRAD 2023 Programa de Pós-graduação em Ciências Aplicadas à Hematologia—PPGH-UEA/HEMOAM, Fundação Hospitalar de Hematologia e Hemoterapia do Amazonas
Reference47 articles.
1. A 5-year surveillance of healthcare-associated infections in a university hospital: A retrospective analysis;Erdem;SAGE Open Med.,2022 2. Annavajhala, M.K., Gomez-Simmonds, A., and Uhlemann, A.C. (2019). Multidrug-resistant Enterobacter cloacae complex emerging as a global, diversifying threat. Front. Microbiol., 10. 3. A systematic review of healthcare-associated infections in Africa: An antimicrobial resistance perspective;Irek;Afr. J. Lab. Med.,2018 4. Han, M., Liu, C., Xie, H., Zheng, J., Zhang, Y., Li, C., Shen, H., and Cao, X. (2023). Genomic and clinical characteristics of carbapenem-resistant Enterobacter cloacae complex isolates collected in a Chinese tertiary hospital during 2013–2021. Front. Microbiol., 14. 5. Phylogenomic analysis of CTX-M-15–producing Enterobacter hormaechei belonging to the high-risk ST78 from animal infection: Another successful One Health clone?;Cardoso;J. Glob. Antimicrob. Resist.,2022
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