PLoS ONE (Jan 2012)

Glycoinositolphospholipids from Trypanosomatids subvert nitric oxide production in Rhodnius prolixus salivary glands.

  • Felipe Gazos-Lopes,
  • Rafael Dias Mesquita,
  • Lívia Silva-Cardoso,
  • Raquel Senna,
  • Alan Barbosa Silveira,
  • Willy Jablonka,
  • Cecília Oliveira Cudischevitch,
  • Alan Brito Carneiro,
  • Ednildo Alcantara Machado,
  • Luize G Lima,
  • Robson Queiroz Monteiro,
  • Roberto Henrique Nussenzveig,
  • Evelize Folly,
  • Alexandre Romeiro,
  • Jorick Vanbeselaere,
  • Lucia Mendonça-Previato,
  • José Osvaldo Previato,
  • Jesus G Valenzuela,
  • José Marcos Chaves Ribeiro,
  • Georgia Correa Atella,
  • Mário Alberto Cardoso Silva-Neto

DOI
https://doi.org/10.1371/journal.pone.0047285
Journal volume & issue
Vol. 7, no. 10
p. e47285

Abstract

Read online

BackgroundRhodnius prolixus is a blood-sucking bug vector of Trypanosoma cruzi and T. rangeli. T. cruzi is transmitted by vector feces deposited close to the wound produced by insect mouthparts, whereas T. rangeli invades salivary glands and is inoculated into the host skin. Bug saliva contains a set of nitric oxide-binding proteins, called nitrophorins, which deliver NO to host vessels and ensure vasodilation and blood feeding. NO is generated by nitric oxide synthases (NOS) present in the epithelium of bug salivary glands. Thus, T. rangeli is in close contact with NO while in the salivary glands.Methodology/principal findingsHere we show by immunohistochemical, biochemical and molecular techniques that inositolphosphate-containing glycolipids from trypanosomatids downregulate NO synthesis in the salivary glands of R. prolixus. Injecting insects with T. rangeli-derived glycoinositolphospholipids (Tr GIPL) or T. cruzi-derived glycoinositolphospholipids (Tc GIPL) specifically decreased NO production. Salivary gland treatment with Tc GIPL blocks NO production without greatly affecting NOS mRNA levels. NOS protein is virtually absent from either Tr GIPL- or Tc GIPL-treated salivary glands. Evaluation of NO synthesis by using a fluorescent NO probe showed that T. rangeli-infected or Tc GIPL-treated glands do not show extensive labeling. The same effect is readily obtained by treatment of salivary glands with the classical protein tyrosine phosphatase (PTP) inhibitor, sodium orthovanadate (SO). This suggests that parasite GIPLs induce the inhibition of a salivary gland PTP. GIPLs specifically suppressed NO production and did not affect other anti-hemostatic properties of saliva, such as the anti-clotting and anti-platelet activities.Conclusions/significanceTaken together, these data suggest that trypanosomatids have overcome NO generation using their surface GIPLs. Therefore, these molecules ensure parasite survival and may ultimately enhance parasite transmission.