Cargando…

Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature

Streptococcus agalactiae is one of the most important pathogens associated with streptococcosis outbreaks in Nile tilapia farms worldwide. High water temperature (above 27°C) has been described as a predisposing factor for the disease in fish. At low temperatures (below 25°C), fish mortalities are n...

Descripción completa

Detalles Bibliográficos
Autores principales: Tavares, Guilherme C., Carvalho, Alex F., Pereira, Felipe L., Rezende, Cristiana P., Azevedo, Vasco A. C., Leal, Carlos A. G., Figueiredo, Henrique C. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224512/
https://www.ncbi.nlm.nih.gov/pubmed/30450092
http://dx.doi.org/10.3389/fmicb.2018.02639
_version_ 1783369613962117120
author Tavares, Guilherme C.
Carvalho, Alex F.
Pereira, Felipe L.
Rezende, Cristiana P.
Azevedo, Vasco A. C.
Leal, Carlos A. G.
Figueiredo, Henrique C. P.
author_facet Tavares, Guilherme C.
Carvalho, Alex F.
Pereira, Felipe L.
Rezende, Cristiana P.
Azevedo, Vasco A. C.
Leal, Carlos A. G.
Figueiredo, Henrique C. P.
author_sort Tavares, Guilherme C.
collection PubMed
description Streptococcus agalactiae is one of the most important pathogens associated with streptococcosis outbreaks in Nile tilapia farms worldwide. High water temperature (above 27°C) has been described as a predisposing factor for the disease in fish. At low temperatures (below 25°C), fish mortalities are not usually observed in farms. Temperature variation can modulate the expression of genes and proteins involved in metabolism, adaptation, and bacterial pathogenicity, thus increasing or decreasing the ability to infect the host. This study aimed to evaluate the transcriptome and proteome of a fish-pathogenic S. agalactiae strain SA53 subjected to in vitro growth at different temperatures using a microarray and label-free shotgun LC-HDMS(E) approach. Biological triplicates of isolates were cultured in BHIT broth at 22 or 32°C for RNA and protein isolation and submitted for transcriptomic and proteomic analyses. In total, 1,730 transcripts were identified in SA53, with 107 genes being differentially expressed between the temperatures evaluated. A higher number of genes related to metabolism, mainly from the phosphotransferase system (PTS) and ATP-binding cassette (ABC) transport system, were upregulated at 32°C. In the proteome analysis, 1,046 proteins were identified in SA53, of which 81 were differentially regulated between 22 and 32°C. Proteins involved in defense mechanisms, lipid transport and metabolism, and nucleotide transport and metabolism were upregulated at 32°C. A higher number of interactions were observed in proteins involved in nucleotide transport and metabolism. We observed a low correlation between the transcriptome and proteome datasets. Our study indicates that the transcriptome and proteome of a fish-adapted S. agalactiae strain are modulated by temperature, particularly showing differential expression of genes/proteins involved in metabolism, virulence factors, and adaptation.
format Online
Article
Text
id pubmed-6224512
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62245122018-11-16 Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature Tavares, Guilherme C. Carvalho, Alex F. Pereira, Felipe L. Rezende, Cristiana P. Azevedo, Vasco A. C. Leal, Carlos A. G. Figueiredo, Henrique C. P. Front Microbiol Microbiology Streptococcus agalactiae is one of the most important pathogens associated with streptococcosis outbreaks in Nile tilapia farms worldwide. High water temperature (above 27°C) has been described as a predisposing factor for the disease in fish. At low temperatures (below 25°C), fish mortalities are not usually observed in farms. Temperature variation can modulate the expression of genes and proteins involved in metabolism, adaptation, and bacterial pathogenicity, thus increasing or decreasing the ability to infect the host. This study aimed to evaluate the transcriptome and proteome of a fish-pathogenic S. agalactiae strain SA53 subjected to in vitro growth at different temperatures using a microarray and label-free shotgun LC-HDMS(E) approach. Biological triplicates of isolates were cultured in BHIT broth at 22 or 32°C for RNA and protein isolation and submitted for transcriptomic and proteomic analyses. In total, 1,730 transcripts were identified in SA53, with 107 genes being differentially expressed between the temperatures evaluated. A higher number of genes related to metabolism, mainly from the phosphotransferase system (PTS) and ATP-binding cassette (ABC) transport system, were upregulated at 32°C. In the proteome analysis, 1,046 proteins were identified in SA53, of which 81 were differentially regulated between 22 and 32°C. Proteins involved in defense mechanisms, lipid transport and metabolism, and nucleotide transport and metabolism were upregulated at 32°C. A higher number of interactions were observed in proteins involved in nucleotide transport and metabolism. We observed a low correlation between the transcriptome and proteome datasets. Our study indicates that the transcriptome and proteome of a fish-adapted S. agalactiae strain are modulated by temperature, particularly showing differential expression of genes/proteins involved in metabolism, virulence factors, and adaptation. Frontiers Media S.A. 2018-11-02 /pmc/articles/PMC6224512/ /pubmed/30450092 http://dx.doi.org/10.3389/fmicb.2018.02639 Text en Copyright © 2018 Tavares, Carvalho, Pereira, Rezende, Azevedo, Leal and Figueiredo. http://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
Tavares, Guilherme C.
Carvalho, Alex F.
Pereira, Felipe L.
Rezende, Cristiana P.
Azevedo, Vasco A. C.
Leal, Carlos A. G.
Figueiredo, Henrique C. P.
Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title_full Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title_fullStr Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title_full_unstemmed Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title_short Transcriptome and Proteome of Fish-Pathogenic Streptococcus agalactiae Are Modulated by Temperature
title_sort transcriptome and proteome of fish-pathogenic streptococcus agalactiae are modulated by temperature
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6224512/
https://www.ncbi.nlm.nih.gov/pubmed/30450092
http://dx.doi.org/10.3389/fmicb.2018.02639
work_keys_str_mv AT tavaresguilhermec transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT carvalhoalexf transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT pereirafelipel transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT rezendecristianap transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT azevedovascoac transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT lealcarlosag transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature
AT figueiredohenriquecp transcriptomeandproteomeoffishpathogenicstreptococcusagalactiaearemodulatedbytemperature