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

Publisher

MDPI AG

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