NADPH Phagocyte Oxidase Knockout Mice Control Trypanosoma cruzi Proliferation, but Develop Circulatory Collapse and Succumb to Infection


Autoria(s): Santiago, Helton C.; Lombana, Claudia Z. Gonzalez; Macedo, Juan P.; Utsch, Lara; Tafuri, Wagner L.; Campagnole-Santos, Maria Jose; Alves, Rosana O.; Filho, José Carlos Farias Alves; Romanha, Alvaro J.; Cunha, Fernando Queiroz; Teixeira, Mauro M.; Radi, Rafael; Vieira, Leda Q.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

07/11/2013

07/11/2013

2012

Resumo

(NO)-N-center dot is considered to be a key macrophage-derived cytotoxic effector during Trypanosoma cruzi infection. On the other hand, the microbicidal properties of reactive oxygen species (ROS) are well recognized, but little importance has been attributed to them during in vivo infection with T. cruzi. In order to investigate the role of ROS in T. cruzi infection, mice deficient in NADPH phagocyte oxidase (gp91(phox-/-) or phox KO) were infected with Y strain of T. cruzi and the course of infection was followed. phox KO mice had similar parasitemia, similar tissue parasitism and similar levels of IFN-gamma and TNF in serum and spleen cell culture supernatants, when compared to wild-type controls. However, all phox KO mice succumbed to infection between day 15 and 21 after inoculation with the parasite, while 60% of wild-type mice were alive 50 days after infection. Further investigation demonstrated increased serum levels of nitrite and nitrate (NOx) at day 15 of infection in phox KO animals, associated with a drop in blood pressure. Treatment with a NOS2 inhibitor corrected the blood pressure, implicating NOS2 in this phenomenon. We postulate that superoxide reacts with (NO)-N-center dot in vivo, preventing blood pressure drops in wild type mice. Hence, whilst superoxide from phagocytes did not play a critical role in parasite control in the phox KO animals, its production would have an important protective effect against blood pressure decline during infection with T. cruzi.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [CNPq473597/2006-3, 304776/2009-2]

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

INCT de Processos Redox em Biomedicina-Redoxoma [CNPq/FAPESP/CAPES573530/2008-4]

National Institutes of Health [1R01AI095173-01]

Howard Hughes Medical Institute

Comision Sectorial de Investigacion Cientifica (CSIC)/Universidad de la Republica, Uruguay

Identificador

PLOS NEGLECTED TROPICAL DISEASES, SAN FRANCISCO, v. 6, n. 2, pp. 102-110, FEB, 2012

1935-2727

http://www.producao.usp.br/handle/BDPI/42999

10.1371/journal.pntd.0001492

http://dx.doi.org/10.1371/journal.pntd.0001492

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS NEGLECTED TROPICAL DISEASES

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #INDUCIBLE NITRIC-OXIDE #CHRONIC GRANULOMATOUS-DISEASE #REACTIVE OXYGEN #TOXOPLASMA-GONDII #OXIDATIVE STRESS #SUPEROXIDE-PRODUCTION #LEISHMANIA-MAJOR #HOST-RESISTANCE #CUTTING EDGE #NO SYNTHASE #INFECTIOUS DISEASES #PARASITOLOGY #TROPICAL MEDICINE
Tipo

article

original article

publishedVersion