Cargando…

Adaptive laboratory evolution of Salmonella enterica in acid stress

INTRODUCTION: Adaptive laboratory evolution (ALE) studies play a crucial role in understanding the adaptation and evolution of different bacterial species. In this study, we have investigated the adaptation and evolution of Salmonella enterica serovar Enteritidis to acetic acid using ALE. MATERIALS...

Descripción completa

Detalles Bibliográficos
Autores principales: Ghoshal, Mrinalini, Bechtel, Tyler D., Gibbons, John G., McLandsborough, Lynne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687551/
https://www.ncbi.nlm.nih.gov/pubmed/38033570
http://dx.doi.org/10.3389/fmicb.2023.1285421
_version_ 1785152000191627264
author Ghoshal, Mrinalini
Bechtel, Tyler D.
Gibbons, John G.
McLandsborough, Lynne
author_facet Ghoshal, Mrinalini
Bechtel, Tyler D.
Gibbons, John G.
McLandsborough, Lynne
author_sort Ghoshal, Mrinalini
collection PubMed
description INTRODUCTION: Adaptive laboratory evolution (ALE) studies play a crucial role in understanding the adaptation and evolution of different bacterial species. In this study, we have investigated the adaptation and evolution of Salmonella enterica serovar Enteritidis to acetic acid using ALE. MATERIALS AND METHODS: Acetic acid concentrations below the minimum inhibitory concentration (sub-MIC) were used. Four evolutionary lineages (EL), namely, EL1, EL2, EL3, and EL4, of S. Enteritidis were developed, each demonstrating varying levels of resistance to acetic acid. RESULTS: The acetic acid MIC of EL1 remained constant at 27 mM throughout 70 days, while the MIC of EL2, EL3, and EL4 increased throughout the 70 days. EL4 was adapted to the highest concentration of acetic acid (30 mM) and demonstrated the highest increase in its MIC against acetic acid throughout the study, reaching an MIC of 35 mM on day 70. The growth rates of the evolved lineages increased over time and were dependent on the concentration of acetic acid used during the evolutionary process. EL4 had the greatest increase in growth rate, reaching 0.33 (h(−1)) after 70 days in the presence of 30 mM acetic acid as compared to EL1, which had a growth rate of 0.2 (h(−1)) after 70 days with no exposure to acetic acid. Long-term exposure to acetic acid led to an increased MIC of human antibiotics such as ciprofloxacin and meropenem against the S. enterica evolutionary lineages. The MIC of ciprofloxacin for EL1 stayed constant at 0.016 throughout the 70 days while that of EL4 increased to 0.047. Bacterial whole genome sequencing revealed single-nucleotide polymorphisms in the ELs in various genes known to be involved in S. enterica virulence, pathogenesis, and stress response including phoP, phoQ, and fhuA. We also observed genome deletions in some of the ELs as compared to the wild-type S. Enteritidis which may have contributed to the bacterial acid adaptation. DISCUSSION: This study highlights the potential for bacterial adaptation and evolution under environmental stress and underscores the importance of understanding the development of cross resistance to antibiotics in S. enterica populations. This study serves to enhance our understanding of the pathogenicity and survival strategies of S. enterica under acetic acid stress.
format Online
Article
Text
id pubmed-10687551
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-106875512023-11-30 Adaptive laboratory evolution of Salmonella enterica in acid stress Ghoshal, Mrinalini Bechtel, Tyler D. Gibbons, John G. McLandsborough, Lynne Front Microbiol Microbiology INTRODUCTION: Adaptive laboratory evolution (ALE) studies play a crucial role in understanding the adaptation and evolution of different bacterial species. In this study, we have investigated the adaptation and evolution of Salmonella enterica serovar Enteritidis to acetic acid using ALE. MATERIALS AND METHODS: Acetic acid concentrations below the minimum inhibitory concentration (sub-MIC) were used. Four evolutionary lineages (EL), namely, EL1, EL2, EL3, and EL4, of S. Enteritidis were developed, each demonstrating varying levels of resistance to acetic acid. RESULTS: The acetic acid MIC of EL1 remained constant at 27 mM throughout 70 days, while the MIC of EL2, EL3, and EL4 increased throughout the 70 days. EL4 was adapted to the highest concentration of acetic acid (30 mM) and demonstrated the highest increase in its MIC against acetic acid throughout the study, reaching an MIC of 35 mM on day 70. The growth rates of the evolved lineages increased over time and were dependent on the concentration of acetic acid used during the evolutionary process. EL4 had the greatest increase in growth rate, reaching 0.33 (h(−1)) after 70 days in the presence of 30 mM acetic acid as compared to EL1, which had a growth rate of 0.2 (h(−1)) after 70 days with no exposure to acetic acid. Long-term exposure to acetic acid led to an increased MIC of human antibiotics such as ciprofloxacin and meropenem against the S. enterica evolutionary lineages. The MIC of ciprofloxacin for EL1 stayed constant at 0.016 throughout the 70 days while that of EL4 increased to 0.047. Bacterial whole genome sequencing revealed single-nucleotide polymorphisms in the ELs in various genes known to be involved in S. enterica virulence, pathogenesis, and stress response including phoP, phoQ, and fhuA. We also observed genome deletions in some of the ELs as compared to the wild-type S. Enteritidis which may have contributed to the bacterial acid adaptation. DISCUSSION: This study highlights the potential for bacterial adaptation and evolution under environmental stress and underscores the importance of understanding the development of cross resistance to antibiotics in S. enterica populations. This study serves to enhance our understanding of the pathogenicity and survival strategies of S. enterica under acetic acid stress. Frontiers Media S.A. 2023-11-16 /pmc/articles/PMC10687551/ /pubmed/38033570 http://dx.doi.org/10.3389/fmicb.2023.1285421 Text en Copyright © 2023 Ghoshal, Bechtel, Gibbons and McLandsborough. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Ghoshal, Mrinalini
Bechtel, Tyler D.
Gibbons, John G.
McLandsborough, Lynne
Adaptive laboratory evolution of Salmonella enterica in acid stress
title Adaptive laboratory evolution of Salmonella enterica in acid stress
title_full Adaptive laboratory evolution of Salmonella enterica in acid stress
title_fullStr Adaptive laboratory evolution of Salmonella enterica in acid stress
title_full_unstemmed Adaptive laboratory evolution of Salmonella enterica in acid stress
title_short Adaptive laboratory evolution of Salmonella enterica in acid stress
title_sort adaptive laboratory evolution of salmonella enterica in acid stress
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687551/
https://www.ncbi.nlm.nih.gov/pubmed/38033570
http://dx.doi.org/10.3389/fmicb.2023.1285421
work_keys_str_mv AT ghoshalmrinalini adaptivelaboratoryevolutionofsalmonellaentericainacidstress
AT bechteltylerd adaptivelaboratoryevolutionofsalmonellaentericainacidstress
AT gibbonsjohng adaptivelaboratoryevolutionofsalmonellaentericainacidstress
AT mclandsboroughlynne adaptivelaboratoryevolutionofsalmonellaentericainacidstress