Reactive nitrogen species induced catalases promote a novel nitrosative stress tolerance mechanism in Vibrio cholerae.


Journal

Nitric oxide : biology and chemistry
ISSN: 1089-8611
Titre abrégé: Nitric Oxide
Pays: United States
ID NLM: 9709307

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 12 09 2018
revised: 04 03 2019
accepted: 09 04 2019
pubmed: 15 4 2019
medline: 4 12 2019
entrez: 15 4 2019
Statut: ppublish

Résumé

Vibrio cholerae faces nitrosative stress during successful colonization in intestine. Very little information is available on the nitrosative stress protective mechanisms of V. cholerae. Reports show that NorR regulon control two genes hmpA and nnrS responsible for nitric oxide (NO) detoxification in V. cholerae. In the present study we first time report a novel role of V. cholerae catalases under nitrosative stress. Using zymogram analysis of catalase we showed that KatB and KatG activity were induced within 30 min in V. cholerae in the presence of sodium nitroprusside (SNP), a NO donor compound. Surprisingly, V. cholerae cell survival was found to be decreased under nitrosative stress if catalase activities were blocked by ATz, a catalase inhibitor. Flow cytometry study was conducted to detect reactive oxygen species (ROS) and reactive nitrogen species (RNS) using DHE and DHR123, fluorescent probes respectively. Short exposure of SNP to V. cholerae did not generate ROS but RNS was detectable within 30 min. Total glutathione content was increased in V. cholerae cells under nitrosative stress. Furthermore, Superoxide dismutase (SOD) and Glutathione reductase (GR) activities remained unchanged under nitrosative stress in V. cholerae indicated antioxidant role of NO which could produce peroxynitrite. To investigate the role of catalase induction under nitrosative stress in V. cholerae, we conducted peroxynitrite reductase assay using cell lysates. Interestingly, SNP treated V. cholerae cell lysates showed lowest DHR123 oxidation compared to the control set. The extent of DHR123 oxidation was more in V. cholerae cell lysate when catalases were blocked by ATz.

Identifiants

pubmed: 30981896
pii: S1089-8603(18)30265-9
doi: 10.1016/j.niox.2019.04.002
pii:
doi:

Substances chimiques

Bacterial Proteins 0
Enzyme Inhibitors 0
Nitric Oxide Donors 0
Reactive Nitrogen Species 0
Nitroprusside 169D1260KM
Catalase EC 1.11.1.6
Amitrole ZF80H5GXUF

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

35-44

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Sourav Kumar Patra (SK)

Department of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, West Bengal, India.

Sourabh Samaddar (S)

Bose Institute, P-1/12, CIT Road Scheme VIIM, Kolkata, 700 054, West Bengal, India.

Nilanjan Sinha (N)

Department of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, West Bengal, India.

Sanjay Ghosh (S)

Department of Biochemistry, University of Calcutta, 35, Ballygunge Circular Road, Kolkata, 700019, West Bengal, India. Electronic address: ghoshs71@hotmail.com.

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Classifications MeSH