Malaria in Kakuma refugee camp, Turkana, Kenya: facilitation of Anopheles arabiensis vector populations by installed water distribution and catchment systems

<p>Abstract</p> <p>Background</p> <p>Malaria is a major health concern for displaced persons occupying refugee camps in sub-Saharan Africa, yet there is little information on the incidence of infection and nature of transmission in these settings. Kakuma Refugee Camp, located in a dry area of north-western Kenya, has hosted ca. 60,000 to 90,000 refugees since 1992, primarily from Sudan and Somalia. The purpose of this study was to investigate malaria prevalence and attack rate and sources of <it>Anopheles </it>vectors in Kakuma refugee camp, in 2005-2006, after a malaria epidemic was observed by staff at camp clinics.</p> <p>Methods</p> <p>Malaria prevalence and attack rate was estimated from cases of fever presenting to camp clinics and the hospital in August 2005, using rapid diagnostic tests and microscopy of blood smears. Larval habitats of vectors were sampled and mapped. Houses were sampled for adult vectors using the pyrethrum knockdown spray method, and mapped. Vectors were identified to species level and their infection with <it>Plasmodium falciparum </it>determined.</p> <p>Results</p> <p>Prevalence of febrile illness with <it>P. falciparum </it>was highest among the 5 to 17 year olds (62.4%) while malaria attack rate was highest among the two to 4 year olds (5.2/1,000/day). Infected individuals were spatially concentrated in three of the 11 residential zones of the camp. The indoor densities of <it>Anopheles arabiensis</it>, the sole malaria vector, were similar during the wet and dry seasons, but were distributed in an aggregated fashion and predominantly in the same zones where malaria attack rates were high. Larval habitats and larval populations were also concentrated in these zones. Larval habitats were man-made pits of water associated with tap-stands installed as the water delivery system to residents with year round availability in the camp. Three percent of <it>A. arabiensis </it>adult females were infected with <it>P. falciparum </it>sporozoites in the rainy season.</p> <p>Conclusions</p> <p>Malaria in Kakuma refugee camp was due mainly to infection with <it>P. falciparum </it>and showed a hyperendemic age-prevalence profile, in an area with otherwise low risk of malaria given prevailing climate. Transmission was sustained by <it>A. arabiensis</it>, whose populations were facilitated by installation of man-made water distribution and catchment systems.</p

The future of African nowcasting

Nowcasting (weather forecasting predictions from zero to several hours) has enormous value and potential in Africa, where populations and economic activity are highly vulnerable to rapidly changing weather conditions. Timely issuing of warnings, a few hours before an event, can enable the public and decision-makers to take action. Rainfall radar estimates are not widely available in Africa, nor likely to be in the coming years, and numerical weather prediction (NWP) currently has low skill over the African continent. Therefore, for the delivery of nowcasting in Africa, satellite products are the best practical option and needed urgently (Roberts et al., 2021). Fifteen minute (or faster) updates of MSG (Meteosat Second Generation) images and NWC-SAF (Nowcasting Satellite Applications Facility) products are crucial for nowcasting to warn users (e.g. fisherfolk on Lake Victoria, flooding in urban areas, etc.) on pending severe storms. The possibility to have such products every 10 minutes, as well as data from the forthcoming MTG (Meteosat Third Generation) lightning imager, would be highly beneficial to all African countries, saving lives and livelihoods where high population growth and the most extreme impacts of climate change combine

Ionic liquid modified poly(2,6-dimethyl-1,4-phenylene oxide) for CO2 separation

Ionic liquid modified poly(2, 6-dimethyl-1, 4-phenylene oxide) (PPO) was synthesized by introducing imidazolium-based, pyridinium-based, and ammonium-basd ionic liquid groups to the methyl position of PPO. Membranes were prepared from the different types of ionic liquid modified PPO (IPPO), and the permeability of CO and N2 in these membranes was characterized. For having the CO -philic ionic liquid groups in the structure, the CO solubility of the IPPO is better than that of PPO, while the CO diffusivity in the IPPO is proportional to glass transition temperatures. The adsorption and desorption of CO in the IPPO were also investigated, and the results manifest that the adsorption and desorption of CO in IPPO are completely reversible, which makes the polymer promising as solid adsorbent materials for CO separation

Unique Effects of Acute Aripiprazole Treatment on the Dopamine D2 Receptor Downstream cAMP-PKA and Akt-GSK3β Signalling Pathways in Rats

Aripiprazole is a wide-used antipsychotic drug with therapeutic effects on both positive and negative symptoms of schizophrenia, and reduced side-effects. Although aripiprazole was developed as a dopamine D2 receptor (D2R) partial agonist, all other D2R partial agonists that aimed to mimic aripiprazole failed to exert therapeutic effects in clinic. The present in vivo study aimed to investigate the effects of aripiprazole on the D2R downstream cAMP-PKA and Akt-GSK3β signalling pathways in comparison with a D2R antagonist - haloperidol and a D2R partial agonist - bifeprunox. Rats were injected once with aripiprazole (0.75mg/kg, i.p.), bifeprunox (0.8mg/kg, i.p.), haloperidol (0.1mg/kg, i.p.) or vehicle. Five brain regions - the prefrontal cortex (PFC), nucleus accumbens (NAc), caudate putamen (CPu), ventral tegmental area (VTA) and substantia nigra (SN) were collected. The protein levels of PKA, Akt and GSK3β were measured by Western Blotting; the cAMP levels were examined by ELISA tests. The results showed that aripiprazole presented similar acute effects on PKA expression to haloperidol, but not bifeprunox, in the CPU and VTA. Additionally, aripiprazole was able to increase the phosphorylation of GSK3β in the PFC, NAc, CPu and SN, respectively, which cannot be achieved by bifeprunox and haloperidol. These results suggested that acute treatment of aripiprazole had differential effects on the cAMP-PKA and Akt-GSK3β signalling pathways from haloperidol and bifeprunox in these brain areas. This study further indicated that, by comparison with bifeprunox, the unique pharmacological profile of aripiprazole may be attributed to the relatively lower intrinsic activity at D2R