Cargando…

The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis

BACKGROUND: Oxidative stress is responsible for generating DNA lesions and the 8-oxoguanine (8-oxoG) is the most commonly lesion found in DNA damage. When this base is incorporated during DNA replication, it could generate double-strand DNA breaks and cellular death. MutT enzyme hydrolyzes the 8-oxo...

Descripción completa

Detalles Bibliográficos
Autores principales: Andrade, Laila de Carvalho, Santi, Ana Maria Murta, Alves, Ceres Luciana, Ferreira, Wesley Roger Rodrigues, de Assis, Antônio Vinícius, Oliveira, Edward, Machado, Carlos Renato, Murta, Silvane Maria Fonseca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337112/
https://www.ncbi.nlm.nih.gov/pubmed/32638832
http://dx.doi.org/10.1590/0074-02760190469
_version_ 1783554448679763968
author Andrade, Laila de Carvalho
Santi, Ana Maria Murta
Alves, Ceres Luciana
Ferreira, Wesley Roger Rodrigues
de Assis, Antônio Vinícius
Oliveira, Edward
Machado, Carlos Renato
Murta, Silvane Maria Fonseca
author_facet Andrade, Laila de Carvalho
Santi, Ana Maria Murta
Alves, Ceres Luciana
Ferreira, Wesley Roger Rodrigues
de Assis, Antônio Vinícius
Oliveira, Edward
Machado, Carlos Renato
Murta, Silvane Maria Fonseca
author_sort Andrade, Laila de Carvalho
collection PubMed
description BACKGROUND: Oxidative stress is responsible for generating DNA lesions and the 8-oxoguanine (8-oxoG) is the most commonly lesion found in DNA damage. When this base is incorporated during DNA replication, it could generate double-strand DNA breaks and cellular death. MutT enzyme hydrolyzes the 8-oxoG from the nucleotide pool, preventing its incorporation during DNA replication. OBJECTIVES: To investigate the importance of 8-oxoG in Leishmania infantum and L. braziliensis, in this study we analysed the impact of heterologous expression of Escherichia coli MutT (EcMutT) enzyme in drug-resistance phenotype and defense against oxidative stress. METHODS: Comparative analysis of L. braziliensis and L. infantum H(2)O(2) tolerance and cell cycle profile were performed. Lines of L. braziliensis and L. infantum expressing EcMutT were generated and evaluated using susceptibility tests to H(2)O(2) and Sb(III), cell cycle analysis, γH2A western blotting, and BrdU native detection assay. FINDINGS: Comparative analysis of tolerance to oxidative stress generated by H(2)O(2) showed that L. infantum is more tolerant to exogenous H(2)O(2) than L. braziliensis. In addition, cell cycle analysis showed that L. infantum, after treatment with H(2)O(2), remains in G1 phase, returning to its normal growth rate after 72 h. In contrast, after treatment with H(2)O(2), L. braziliensis parasites continue to move to the next stages of the cell cycle. Expression of the E. coli MutT gene in L. braziliensis and L. infantum does not interfere in parasite growth or in susceptibility to Sb(III). Interestingly, we observed that L. braziliensis EcMutT-expressing clones were more tolerant to H(2)O(2) treatment, presented lower activation of γH2A, a biomarker of genotoxic stress, and lower replication stress than its parental non-transfected parasites. In contrast, the EcMutT is not involved in protection against oxidative stress generated by H(2)O(2) in L. infantum. MAIN CONCLUSIONS: Our results showed that 8-oxoG clearance in L. braziliensis is important to avoid misincorporation during DNA replication after oxidative stress generated by H(2)O(2).
format Online
Article
Text
id pubmed-7337112
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Instituto Oswaldo Cruz, Ministério da Saúde
record_format MEDLINE/PubMed
spelling pubmed-73371122020-07-10 The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis Andrade, Laila de Carvalho Santi, Ana Maria Murta Alves, Ceres Luciana Ferreira, Wesley Roger Rodrigues de Assis, Antônio Vinícius Oliveira, Edward Machado, Carlos Renato Murta, Silvane Maria Fonseca Mem Inst Oswaldo Cruz Original Article BACKGROUND: Oxidative stress is responsible for generating DNA lesions and the 8-oxoguanine (8-oxoG) is the most commonly lesion found in DNA damage. When this base is incorporated during DNA replication, it could generate double-strand DNA breaks and cellular death. MutT enzyme hydrolyzes the 8-oxoG from the nucleotide pool, preventing its incorporation during DNA replication. OBJECTIVES: To investigate the importance of 8-oxoG in Leishmania infantum and L. braziliensis, in this study we analysed the impact of heterologous expression of Escherichia coli MutT (EcMutT) enzyme in drug-resistance phenotype and defense against oxidative stress. METHODS: Comparative analysis of L. braziliensis and L. infantum H(2)O(2) tolerance and cell cycle profile were performed. Lines of L. braziliensis and L. infantum expressing EcMutT were generated and evaluated using susceptibility tests to H(2)O(2) and Sb(III), cell cycle analysis, γH2A western blotting, and BrdU native detection assay. FINDINGS: Comparative analysis of tolerance to oxidative stress generated by H(2)O(2) showed that L. infantum is more tolerant to exogenous H(2)O(2) than L. braziliensis. In addition, cell cycle analysis showed that L. infantum, after treatment with H(2)O(2), remains in G1 phase, returning to its normal growth rate after 72 h. In contrast, after treatment with H(2)O(2), L. braziliensis parasites continue to move to the next stages of the cell cycle. Expression of the E. coli MutT gene in L. braziliensis and L. infantum does not interfere in parasite growth or in susceptibility to Sb(III). Interestingly, we observed that L. braziliensis EcMutT-expressing clones were more tolerant to H(2)O(2) treatment, presented lower activation of γH2A, a biomarker of genotoxic stress, and lower replication stress than its parental non-transfected parasites. In contrast, the EcMutT is not involved in protection against oxidative stress generated by H(2)O(2) in L. infantum. MAIN CONCLUSIONS: Our results showed that 8-oxoG clearance in L. braziliensis is important to avoid misincorporation during DNA replication after oxidative stress generated by H(2)O(2). Instituto Oswaldo Cruz, Ministério da Saúde 2020-07-06 /pmc/articles/PMC7337112/ /pubmed/32638832 http://dx.doi.org/10.1590/0074-02760190469 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Article
Andrade, Laila de Carvalho
Santi, Ana Maria Murta
Alves, Ceres Luciana
Ferreira, Wesley Roger Rodrigues
de Assis, Antônio Vinícius
Oliveira, Edward
Machado, Carlos Renato
Murta, Silvane Maria Fonseca
The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title_full The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title_fullStr The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title_full_unstemmed The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title_short The heterologous expression of Escherichia coli MutT enzyme is involved in the protection against oxidative stress in Leishmania braziliensis
title_sort heterologous expression of escherichia coli mutt enzyme is involved in the protection against oxidative stress in leishmania braziliensis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337112/
https://www.ncbi.nlm.nih.gov/pubmed/32638832
http://dx.doi.org/10.1590/0074-02760190469
work_keys_str_mv AT andradelailadecarvalho theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT santianamariamurta theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT alvesceresluciana theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT ferreirawesleyrogerrodrigues theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT deassisantoniovinicius theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT oliveiraedward theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT machadocarlosrenato theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT murtasilvanemariafonseca theheterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT andradelailadecarvalho heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT santianamariamurta heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT alvesceresluciana heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT ferreirawesleyrogerrodrigues heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT deassisantoniovinicius heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT oliveiraedward heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT machadocarlosrenato heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis
AT murtasilvanemariafonseca heterologousexpressionofescherichiacolimuttenzymeisinvolvedintheprotectionagainstoxidativestressinleishmaniabraziliensis