The Molecular Biology of Insect Disease Vectors 1997
DOI: 10.1007/978-94-009-1535-0_13
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Infection of triatomines with Trypanosoma cruzi

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Cited by 12 publications
(10 citation statements)
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“…66,67 We placed each jar of nymphs under an artificial membrane feeder containing the parasite-blood solution at 37.5°C for about 30 minutes. 68 Control insects consumed blood without parasites. We weighed each nymph after feeding to estimate the number of parasites ingested, which was calculated by subtracting each insect's pre-feeding weight from its postfeeding weight, dividing this amount by the average density of human blood (1.06 mg/mL), and multiplying the result by 3.3-3.5 × 10 6 flagellates per milliliter, depending on parasite treatment.…”
Section: Methodsmentioning
confidence: 99%
“…66,67 We placed each jar of nymphs under an artificial membrane feeder containing the parasite-blood solution at 37.5°C for about 30 minutes. 68 Control insects consumed blood without parasites. We weighed each nymph after feeding to estimate the number of parasites ingested, which was calculated by subtracting each insect's pre-feeding weight from its postfeeding weight, dividing this amount by the average density of human blood (1.06 mg/mL), and multiplying the result by 3.3-3.5 × 10 6 flagellates per milliliter, depending on parasite treatment.…”
Section: Methodsmentioning
confidence: 99%
“…Specimens that were completely desiccated at the time of processing were excluded. For specimens collected during field studies, the digestive tract was removed (Garcia and De Azambuja 1997) using sterile forceps and scalpel, and placed in 50 μ l phosphate-buffered saline. Samples were flash-frozen in an ethanol + dry ice bath and stored on dry ice until transported to the laboratory, where they were stored at –70°C until processed.…”
Section: Methodsmentioning
confidence: 99%
“…The posterior mid-and hindgut from each newly collected bug was dissected following previously described methods (Garcia and De Azambuja 1997) using sterile, disposable scalpels and forceps disinfected with a 10% bleach solution and ultrapure water rinse between samples. The excised gut was placed in 50-L of molecular-grade water and homogenized using a sterile, disposable pestle.…”
Section: Detection Of T Cruzi In New Specimensmentioning
confidence: 99%