Polymyxin Resistance in Salmonella: Exploring Mutations and Genetic Determinants of Non-Human Isolates

Author:

Vieira Thais1,Dos Santos Carla Adriana1,de Jesus Bertani Amanda Maria1,Costa Gisele Lozano1,Campos Karoline Rodrigues1ORCID,Sacchi Cláudio Tavares1ORCID,Cunha Marcos Paulo Vieira2ORCID,Carvalho Eneas3,da Costa Alef Janguas3ORCID,de Paiva Jacqueline Boldrin4,Rubio Marcela da Silva5ORCID,Camargo Carlos Henrique1ORCID,Tiba-Casas Monique Ribeiro1ORCID

Affiliation:

1. Adolfo Lutz Institute, São Paulo 01246-000, SP, Brazil

2. School of Veterinary Medicine, University of São Paulo, São Paulo 05508-270, SP, Brazil

3. Butantan Institute, São Paulo 05503-900, SP, Brazil

4. R&D Department BioCamp Laboratories, Campinas 13082-020, SP, Brazil

5. School of Agriculture and Veterinarian Sciences, University of the State of São Paulo, Jaboticabal 14884-900, SP, Brazil

Abstract

Until 2015, polymyxin resistance was primarily attributed to chromosomal mutations. However, with the first report of mobile colistin resistance (mcr-1) in commensal Escherichia coli from food animals in China, the landscape has changed. To evaluate the presence of polymyxin resistance in Salmonella spp., a drop screening test for colistin and polymyxin B was carried out on 1156 isolates of non-human origin (animals, food, and the environment), received in Brazil, between 2016 and 2021. Subsequently, 210 isolates with resistant results in the drop test were subjected to the gold-standard test (broth microdilution) for both colistin and polymyxin B. Whole-genome sequencing (WGS) of 102 resistant isolates was performed for a comprehensive analysis of associated genes. Surprisingly, none of the isolates resistant to colistin in the drop test harbored any of the mcr variants (mcr-1 to mcr-10). WGS identified that the most common mutations were found in pmrA (n= 22; T89S) and pmrB (n = 24; M15T, G73S, V74I, I83A, A111V). Other resistance determinants were also detected, such as the aac(6′)-Iaa gene in 72 isolates, while others carried beta-lactamase genes (blaTEM-1 blaCTX-M-2, blaCMY-2). Additionally, genes associated with fluoroquinolone resistance (qnrB19, qnrS1, oqxA/B) were detected in 11 isolates. Colistin and polymyxin B resistance were identified among Salmonella from non-human sources, but not associated with the mcr genes. Furthermore, the already-described mutations associated with polymyxin resistance were detected in only a small number of isolates, underscoring the need to explore and characterize unknown genes that contribute to resistance.

Funder

São Paulo Research Foundation

Conselho Nacional de Desenvolvimento Científico e Tecnológico

FESIMA

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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