Abstract:The insect Rhodnius prolixus is responsible for the transmission of Trypanosoma cruzi, which is the etiological agent of Chagas disease in areas of Central and South America. Besides this, it can be infected by other trypanosomes such as Trypanosoma rangeli. The effects of these parasites on vectors are poorly understood and are often controversial so here we focussed on possible negative effects of these parasites on the reproductive performance of R. prolixus, specifically comparing infected and uninfected c… Show more
“…This parasite concentration is similar to that used in several other published studies of T. cruzi infection in triatomines, 9,44,46,50,[54][55][56][57][58][59] and blood meals taken by triatomines at this parasite concentration lead to infective doses that fall within the range of peak parasitemias observed in mice and guinea pigs experimentally infected with T. cruzi. 25,27,[60][61][62][63] Insect infection: insect preparation and feeding.…”
Section: Methodssupporting
confidence: 80%
“…Epimastigote forms of T. cruzi were cultured at 28°C in RPMI-1640 liquid medium (Sigma-Aldrich, St. Louis, MO) supplemented with 10% fetal bovine serum 42,43 and collected in their exponential growth phase for insect infection, as in several similar studies. 9,38,[44][45][46][47][48][49][50][51] To calculate the parasite concentration in culture medium, we gently swished flasks containing the parasites in the medium to facilitate even parasite dispersion. We pipetted the parasites into a 0.5% formalin-phosphate-buffered saline (PBS) solution, and then counted them in a Neubauer cell counter under a compound light microscope.…”
Abstract. The effect of a parasite on the life history of its vector is important for understanding and predicting disease transmission. Chagas disease agent Trypanosoma cruzi is a generalist parasite that is diverse across scales from its genetic diversity to the 100s of mammal and vector species it infects. Its vertebrate hosts show quite variable responses to infection, however, to date there are no studies looking at how T. cruzi variability might result in variable outcomes in its invertebrate host. Therefore, we investigated the effect of different T. cruzi I strains on Rhodnius prolixus survival and development. We found significant variation between insects infected with different strains, with some strains having no effect, as compared with uninfected insects, and others with significantly lower survival and development. We also found that different variables had varying importance between strains, with the effect of time postinfection and the blood:weight ratio of the infective meal significantly affecting the survival of insects infected with some strains, but not others. Our results suggest that T. cruzi can be pathogenic not only to its vertebrate hosts but also to its invertebrate hosts.
“…This parasite concentration is similar to that used in several other published studies of T. cruzi infection in triatomines, 9,44,46,50,[54][55][56][57][58][59] and blood meals taken by triatomines at this parasite concentration lead to infective doses that fall within the range of peak parasitemias observed in mice and guinea pigs experimentally infected with T. cruzi. 25,27,[60][61][62][63] Insect infection: insect preparation and feeding.…”
Section: Methodssupporting
confidence: 80%
“…Epimastigote forms of T. cruzi were cultured at 28°C in RPMI-1640 liquid medium (Sigma-Aldrich, St. Louis, MO) supplemented with 10% fetal bovine serum 42,43 and collected in their exponential growth phase for insect infection, as in several similar studies. 9,38,[44][45][46][47][48][49][50][51] To calculate the parasite concentration in culture medium, we gently swished flasks containing the parasites in the medium to facilitate even parasite dispersion. We pipetted the parasites into a 0.5% formalin-phosphate-buffered saline (PBS) solution, and then counted them in a Neubauer cell counter under a compound light microscope.…”
Abstract. The effect of a parasite on the life history of its vector is important for understanding and predicting disease transmission. Chagas disease agent Trypanosoma cruzi is a generalist parasite that is diverse across scales from its genetic diversity to the 100s of mammal and vector species it infects. Its vertebrate hosts show quite variable responses to infection, however, to date there are no studies looking at how T. cruzi variability might result in variable outcomes in its invertebrate host. Therefore, we investigated the effect of different T. cruzi I strains on Rhodnius prolixus survival and development. We found significant variation between insects infected with different strains, with some strains having no effect, as compared with uninfected insects, and others with significantly lower survival and development. We also found that different variables had varying importance between strains, with the effect of time postinfection and the blood:weight ratio of the infective meal significantly affecting the survival of insects infected with some strains, but not others. Our results suggest that T. cruzi can be pathogenic not only to its vertebrate hosts but also to its invertebrate hosts.
“…rangeli is considered to be pathogenic to its invertebrate hosts, being responsible for triatomine death (1,6,41,42). It is known that several aspects of the physiology of the triatomines are altered during infection by T. rangeli, including reduced immune responses, anti-hemostatic activity of the salivary glands, and behavioral changes such as molting delays, changes in the movements of the insects, decreased reproductive performance and increased mortality (29,43,44). However, the mortality rates in our study were much higher than those observed in other studies analyzing T. rangeli experimental infection (2,25).…”
Introduction: Specific host-parasite associations have been detected experimentally and suggest that triatomines of the genus Rhodnius act as biological filters in the transmission of Trypanosoma rangeli. Objective: To analyze the susceptibility of four Rhodnius species (Rhodnius robustus, Rhodnius neglectus, Rhodnius nasutus and Rhodnius pictipes) to a Brazilian strain of T. rangeli (SC-58/KP1-).
Materials and methods:We selected thirty nymphs of each species, which were fed on blood infected with T. rangeli. Periodically, samples of feces and hemolymph were analyzed. Triatomines with T. rangeli in their hemolymph were fed on mice to check for transmission by bites. Later, the triatomines were dissected to confirm salivary gland infection. Results: Specimens of R. pictipes showed higher rates of intestinal infection compared to the other three species. Epimastigotes and trypomastigotes were detected in hemolymph of four species; however, parasitism was lower in the species of the R. robustus lineage. Rhodnius robustus and R. neglectus specimens did not transmit T. rangeli by bite; after dissection, their glands were not infected. Only one specimen of R. nasutus and two of R. pictipes transmitted the parasite by bite. The rate of salivary gland infection was 16% for R. pictipes and 4% for R. nasutus. Conclusions: Both infectivity (intestinal, hemolymphatic and glandular) and transmission of T. rangeli (SC58/KP1-) were greater and more efficient in R. pictipes. These results reinforce the hypothesis that these triatomines may act as biological filters in the transmission of T. rangeli.
“…prolixus , within 3–4 days post-moult, were fed on inactivated rabbit blood (37°C/20min) with culture epimastigotes (parasite) added at a concentration of 1x10 7 parasites/ml. The control was only inactivated blood added with the same amount of culture medium used in the blood with contained parasites [22]. Upon feeding, insects were housed in a temperature-control chamber at 26°C until moulting to the third instar.…”
Entomopathogenic fungi have been investigated as an alternative tool for controlling various insects, including triatomine vectors of the protozoan Trypanosoma cruzi, the etiological agent of Chagas disease. Here we tested the pathogenicity and virulence of ten isolates of the fungi Metarhizium spp. and Beauveria bassiana against Rhodnius prolixus and found all of the isolates to be virulent. We used two isolates (URPE-11 Metarhizium anisopliae and ENT-1 Beauveria bassiana) for further screening based on their prolific sporulation in vitro (an important property of fungal biopesticides). We characterized their virulences in a dose-response experiment and then examined virulence across a range of temperatures (21, 23, 27 and 30°C). We found isolate ENT-1 to maintain higher levels of virulence over these temperatures than URPE-11. We therefore used B. bassiana ENT-1 in the final experiment in which we examined the survival of insects parasitized with T. cruzi and then infected with this fungus (once again over a range of temperatures). Contrary to our expectations, the survival of insects challenged with the pathogenic fungus was greater when they had previously been infected with the parasite T. cruzi than when they had not (independent of temperature). We discuss these results in terms of aspects of the biologies of the three organisms. In practical terms, we concluded that, while we have fungal isolates of potential interest for development as biopesticides against R. prolixus, we have identified what could be a critical problem for this biological tool: the parasite T. cruzi appears to confer a measure of resistance to the insect against the potential biopesticide agent so use of this fungus as a biopesticide could lead to selection for vector competence.
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