scholarly journals Role of PheE15 Gate in Ligand Entry and Nitric Oxide Detoxification Function of Mycobacterium tuberculosis Truncated Hemoglobin N

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e49291 ◽  
Author(s):  
Ana Oliveira ◽  
Sandeep Singh ◽  
Axel Bidon-Chanal ◽  
Flavio Forti ◽  
Marcelo A. Martí ◽  
...  
2006 ◽  
Vol 34 (1) ◽  
pp. 195-196 ◽  
Author(s):  
G.E. Meakin ◽  
B.J.N. Jepson ◽  
D.J. Richardson ◽  
E.J. Bedmar ◽  
M.J. Delgado

The identification of nitric oxide-bound leghaemoglobin within soya bean nodules has led to the question of how Bradyrhizobium japonicum bacteroids overcome the toxicity of this nitric oxide. It has previously been shown that one candidate for nitric oxide detoxification, the respiratory nitric oxide reductase, is expressed in soya bean nodules from plants supplied with nitrate [Mesa, de Dios Alché, Bedmar and Delgado (2004) Physiol. Plant. 120, 205–211]. In this paper, the role of this enzyme in nitric oxide detoxification is assessed and discussion is provided on other possible B. japonicum nitric oxide detoxification systems.


2009 ◽  
Vol 97 (11) ◽  
pp. 2967-2977 ◽  
Author(s):  
Richard Daigle ◽  
Julie-Anne Rousseau ◽  
Michel Guertin ◽  
Patrick Lagüe

2001 ◽  
Vol 69 (12) ◽  
pp. 7711-7717 ◽  
Author(s):  
Charles A. Scanga ◽  
Vellore P. Mohan ◽  
Kathryn Tanaka ◽  
David Alland ◽  
JoAnne L. Flynn ◽  
...  

ABSTRACT Murine macrophages effect potent antimycobacterial function via the production of nitric oxide by the inducible isoform of the enzyme nitric oxide synthase (NOS2). The protective role of reactive nitrogen intermediates (RNI) against Mycobacterium tuberculosisinfection has been well established in various murine experimental tuberculosis models using laboratory strains of the tubercle bacillus to establish infection by the intravenous route. However, important questions remain about the in vivo importance of RNI in host defense against M. tuberculosis. There is some evidence that RNI play a lesser role following aerogenic, rather than intravenous,M. tuberculosis infection of mice. Furthermore, in vitro studies have demonstrated that different strains of M. tuberculosis, including clinical isolates, vary widely in their susceptibility to the antimycobacterial effects of RNI. Thus, we sought to test rigorously the protective role of RNI against infection with recent clinical isolates of M. tuberculosis following both aerogenic and intravenous challenges. Three recently isolated and unique M. tuberculosis strains were used to infect both wild-type (wt) C57BL/6 and NOS2 gene-disrupted mice. Regardless of the route of infection, NOS2−/− mice were much more susceptible than wt mice to any of the clinical isolates or to either the Erdman or H37Rv laboratory strain of M. tuberculosis. Mycobacteria replicated to much higher levels in the organs of NOS2−/− mice than in those of wt mice. Although the clinical isolates all exhibited enhanced virulence in NOS2−/− mice, they displayed distinct growth rates in vivo. The present study has provided results indicating that RNI are required for the control of murine tuberculous infection caused by both laboratory and clinical strains of M. tuberculosis. This protective role of RNI is essential for the control of infection established by either intravenous or aerogenic challenge.


2006 ◽  
Vol 188 (4) ◽  
pp. 1364-1372 ◽  
Author(s):  
Yaswant K. Dayaram ◽  
Meliza T. Talaue ◽  
Nancy D. Connell ◽  
Vishwanath Venketaraman

ABSTRACT Glutathione is a tripeptide and antioxidant, synthesized at high levels by cells during the production of reactive oxygen and nitrogen intermediates. Glutathione also serves as a carrier molecule for nitric oxide in the form of S-nitrosoglutathione. Previous studies from this laboratory have shown that glutathione and S-nitrosoglutathione are directly toxic to mycobacteria. Glutathione is not transported into the cells as a tripeptide. Extracellular glutathione is converted to a dipeptide due to the action of transpeptidase, and the dipeptide is then transported into the bacterial cells. The processing of glutathione and S-nitrosoglutathione is brought about by the action of the enzyme γ-glutamyl transpeptidase. The function of γ-glutamyl transpeptidase is to cleave glutathione and S-nitrosoglutathione to the dipeptide (Cys-Gly), which is then transported into the bacterium by the multicomponent ABC transporter dipeptide permease. We have created a mutant strain of Mycobacterium tuberculosis lacking this metabolic enzyme. We investigated the sensitivity of this strain to glutathione and S-nitrosoglutathione compared to that of the wild-type bacteria. In addition, we examined the role of glutathione and/or S-nitrosoglutathione in controlling the growth of intracellular M. tuberculosis inside mouse macrophages.


2009 ◽  
Vol 284 (21) ◽  
pp. 14457-14468 ◽  
Author(s):  
Amrita Lama ◽  
Sudesh Pawaria ◽  
Axel Bidon-Chanal ◽  
Arvind Anand ◽  
José Luis Gelpí ◽  
...  

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