Parasitóides (Braconidae) associados à Anastrepha (Tephritidae) em frutos hospedeiros do litoral sul da Bahia

Dentre os organismos que atuam no controle biológico natural dos tefritídeos, os representantes da família Braconidae constituem-se no mecanismo de parasitismo natural mais atuante, e na região Neotropical, representantes de Opiinae são os principais agentes de controle de Anastrepha. Este trabalho teve por objetivo conhecer a percentagem de parasitismo e as espécies de braconídeos associados às fruteiras cultivadas em municípios da região Litoral Sul da Bahia. No período de agosto de 2005 a março de 2008, coletaram-se frutos hospedeiros de moscas-das-frutas de diversas espécies botânicas, e dos frutos foram obtidas as seguintes espécies de Anastrepha: A. fraterculus, A. obliqua, A. bahiensis, A serpentina, A. sororcula e A. zenildae. Do total de 838 exemplares de braconídeos, 21,36% foram da espécie Utetes anastrephae (Viereck), provenientes de cajá, carambola, goiaba, manga e pitanga; 4,42% da espécie Asobara anastrephae (Muesebeck) obtidos dos frutos de cajá, carambola e goiaba, e apenas um exemplar da espécie Opius bellus Gahan (0,12%) que emergiu da amostra de goiaba. A espécie Doryctobracon areolatus (Szépligeti) (74,10%) foi predominante e emergiu dos pupários provenientes de todos os frutos hospedeiros coletados, provavelmente pela maior eficiência desta espécie em localizar as larvas dos tefritídeos. A percentagem média de parasitismo de Anastrepha spp. foi de 4,45%.

Heme oxygenase-1 activity is involved in the control of Toxoplasma gondii infection in the lung of BALB/c and C57BL/6 and in the small intestine of C57BL/6 mice

Heme oxygenase-1 (HO-1) is an enzyme that catabolizes free heme, which induces an intense inflammatory response. The expression of HO-1 is induced by different stimuli, triggering an anti-inflammatory response during biological stress. It was previously verified that HO-1 is able to induce indoleamine 2,3-dioxygenase (IDO), an enzyme that is induced by IFN-γ in Toxoplasma gondii infection. To verify the role of HO-1 during in vivo T. gondii infection, BALB/c and C57BL/6 mice were infected with the ME49 strain and treated with zinc protoporphyrin IX (ZnPPIX) or hemin, which inhibit or induce HO-1 activity, respectively. The results show that T. gondii infection induced high levels of HO-1 expression in the lung of BALB/c and C57BL6 mice. The animals treated with ZnPPIX presented higher parasitism in the lungs of both lineages of mice, whereas hemin treatment decreased the parasite replication in this organ and in the small intestine of infected C57BL/6 mice. Furthermore, C57BL/6 mice infected with T. gondii and treated with hemin showed higher levels of IDO expression in the lungs and small intestine than uninfected mice. In conclusion, our data suggest that HO-1 activity is involved in the control of T. gondii in the lungs of both mouse lineages, whereas the hemin, a HO-1 inducer, seems to be involved in the control of parasitism in the small intestine of C57BL/6 mice.

Proteome of Rhipicephalus sanguineus tick saliva induced by the secretagogues pilocarpine and dopamine

One dimensional gel electrophoresis was used to separate proteins from the saliva of Rhipicephalus sanguineus female ticks fed on rabbits. Gel slices were subjected to tryptic digestion and analyzed by reversed-phase HPLC followed by MS/MS analysis. The data were compared to a database of salivary proteins of the same tick and to the predicted proteins of the host. Saliva was obtained by either pilocarpine or dopamine stimulation of partially fed ticks. Electrophoretic separations of both yielded products that were identified by mass spectrometry, although the pilocarpine-derived sample was of much better quality. The majority of identified proteins were of rabbit origin, indicating the recycling of the host proteins in the tick saliva, including hemoglobin, albumin, haptoglobin, transferring, and a plasma serpin. The few proteins found that were previously associated with parasitism and blood feeding include 2 glycine-rich, cement-like proteins, 2 lipocalins, and a thyropin protease inhibitor. Among other of the 19 tick proteins identified, albeit with undefined roles, were SPARC and cyclophilin A. This catalog provides a resource that can be mined for secreted molecules that play a role in tick–host interactions.