Biomedical subjects

John I Githure

Publications and source records attributed to John I Githure.

22 records · Page 2Linked to original sources

PubMed2003

Determination of Anopheles gambiae larval DNA in the gut of insectivorous dragonfly (Libellulidae) nymphs by polymerase chain reaction.

We examined the predator-prey relationship between larvae of the malaria mosquito Anopheles gambiae and nymphs of the dragonfly (Libellulidae). Studies were conducted to determine whether polymerase chain reaction (PCR) can be used to detect DNA of An. gambiae in the gut of libellulid nymphs, and to determine how long after feeding on An. gambiae that mosquito DNA remains detectable by PCR. Total DNA was extracted from the gut contents of libellulid nymphs by using 2 types of DNA extraction methods. The target sequence for the diagnostic PCR was the intergenic spacer regions of the ribosomal DNA gene locus. These sequences were analyzed by using An. gambiae complex-specific primers. After analyzing nymphal gut contents with PCR at regular postfeed intervals, a 390-base pair product could be amplified. The presence of mosquito larvae was visually confirmed for up to 40 min after feeding. Regardless of the number of mosquito larvae ingested, libellulid gut contents could be amplified or visually seen up to 1 h of digestion. This result indicates the nymphs have a high rate of digestion and that PCR with An. gambiae complex primers will be best utilized within 1 h after feeding as a detection system. This study confirmed that dragonfly nymphs feed well on anopheline larvae, and that mosquito DNA, although rapidly digested, can be successfully recovered and detected from within nymphal digestive tracts.

Animals↗

PubMed2003

Spatial and temporal heterogeneity of Anopheles mosquitoes and Plasmodium falciparum transmission along the Kenyan coast.

The seasonal dynamics and spatial distributions of Anopheles mosquitoes and Plasmodium falciparum parasites were studied for one year at 30 villages in Malindi, Kilifi, and Kwale Districts along the coast of Kenya. Anopheline mosquitoes were sampled inside houses at each site once every two months and malaria parasite prevalence in local school children was determined at the end of the entomologic survey. A total of 5,476 Anopheles gambiae s.l. and 3,461 An. funestus were collected. Species in the An. gambiae complex, identified by a polymerase chain reaction, included 81.9% An. gambiae s.s., 12.8% An. arabiensis, and 5.3% An. merus. Anopheles gambiae s.s. contributed most to the transmission of P. falciparum along the coast as a whole, while An. funestus accounted for more than 50% of all transmission in Kwale District. Large spatial heterogeneity of transmission intensity (< 1 up to 120 infective bites per person per year) resulted in correspondingly large and significantly related variations in parasite prevalence (range = 38-83%). Thirty-two percent of the sites (7 of 22 sites) with malaria prevalences ranging from 38% to 70% had annual entomologic inoculation rates (EIR) less than five infective bites per person per year. Anopheles gambiae s.l. and An. funestus densities in Kwale were not significantly influenced by rainfall. However, both were positively correlated with rainfall one and three months previously in Malindi and Kilifi Districts, respectively. These unexpected variations in the relationship between mosquito populations and rainfall suggest environmental heterogeneity in the predominant aquatic habitats in each district. One important conclusion is that the highly non-linear relationship between EIRs and prevalence indicates that the consistent pattern of high prevalence might be governed by substantial variation in transmission intensity measured by entomologic surveys. The field-based estimate of entomologic parameters on a district level does not provide a sensitive indicator of transmission intensity in this study.

Animals↗

PubMed2003

Blood-meal analysis for anopheline mosquitoes sampled along the Kenyan coast.

A total of 1,480 Anopheles gambiae sensu lato and 439 An. funestus, collected from 30 sites along the Kenyan coast, were tested by direct enzyme-linked immunosorbent assay (ELISA) for blood-meal identification. Overall, the enzyme-linked immunosorbent assay (ELISA) identified 92 and 87% of the samples tested in An. gambiae s.l. and An. funestus, respectively. Of these, human IgG was detected in 98.97% (n = 1,347) of An. gambiae s.l. and 99.48% (n = 379) of An. funestus. Only 14 (1.03%) of the An. gambiae s.l. had fed on other vertebrate hosts tested, which were bovines, chickens, and goats. Additionally, only 2 An. funestus had fed on goats. In all the 28 sites that had bloodfed mosquitoes, An. gambiae s.l. had a human blood index greater than 0.9. Twenty-five of these sites had a human blood index greater than 0.9 for An. funestus, while the other 3 sites had no bloodfed mosquitoes. The An. gambiae s.l. were tested by polymerase chain reaction (PCR) for species identification. A total of 338 were An. gambiae s.s., 79 were An. arabiensis, and 12 were An. merus. The human blood index was 0.96, 0.91, and 1.0 for An. gambiae s.s., An. arabiensis, and An. merus, respectively. The Plasmodium falciparum sporozoite infection rates were 6.2% for species in the An. gambiae complex and 3.7% for An. funestus. These results emphasize that An. funestus and members of the An. gambiae complex on the Kenyan coast are highly anthropophilic, with nearly all specimens feeding on humans during every blood meal. The results further demonstrated active transmission of P. falciparum sporozoites by the primary vector species. This study suggests that the use of insecticide-treated nets will be effective for controlling biting mosquitoes inside houses along the coast of Kenya.

Animals↗

PubMedDate not supplied

An individual-based model of Plasmodium falciparum malaria transmission on the coast of Kenya.

Individual-based models provide powerful tools to model complex interactions characterized by individual variability. This paper presents an object-oriented design for individual-based modelling of Plasmodium falciparum malaria transmission. Two kinds of objects, human and mosquito, that exhibit variability among individuals for parameters such as recovery and survival rates are defined. The model tracks the dynamics of human hosts and adult female mosquitoes individually. Immunity, modelled as a function of exposure history, is represented by reduced susceptibility and increased recovery rate. The model was calibrated using epidemiological data collected at 30 sites along the coast of Kenya. The sites were grouped into low, intermediate and high transmission based on mean daily human-biting rates. Simulation results show that malaria transmission was stable even in low transmission areas where the human-biting rate is approximately 0.5 bite per day. The model was used to examine the effect of infection control programmes that aim at interrupting transmission by reducing human-vector contact rates and implementing active case detection and drug treatment of infections. With this intervention, local elimination of malaria is likely with a probability of extinction of approximately 0.8 in low transmission areas. However, a small amount of immigration (> 0.3%) by infected people into the community could prevent local extinction of the parasite. In intermediate and high transmission areas, reduction in prevalence is short-lived and the probability of local elimination is low, even at high coverage levels of the intervention.

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