STOP ZIKA, MALARIA & OTHER FEVERS

PREVENT Malaria, Zika, Dengue, Typhus, Yellow Fever & West Nile Virus

Based on the 2009 Study "Anais da Academia Brasileira de Ciencias"

Last century (1950s) airplanes were used in the USA and Europe to spray DDT to kill malaria mosquitoes and louse borne typhus. Now 2016 there is a nontoxic, affordable and pure organic Moringa Oil alternative that does not kill the insects but prevents its larvae to come out. A little coating of the oil atop exposed water containers will help destroy mosquito larvae, and thus reduce the threat of malaria and other deadly insect-borne diseases. The seed cake remaining after oil extraction may be used as a fertilizer or as a flocculent to purify water. Aerial spraying is simple and does not require big amounts to cover vast (water) areas. Because the oil is pure organic it does not have any negative affect on the environment nor the health of people and animals, on the contrary, because the oil is considered as a plant growth enhancer.

Let us produce and spray this oil in big quantities to quickly kick Zika, Malaria, Typhus, West Nile Virus, Yellow Fever, and Dengue out of Africa and South America.

SUFFOCATE LARVAE

The study, reported in the June 2009 issue of "Anais da Academia Brasileira de Ciencias," investigated the larvicidal effect of moringa seed extract. The researchers found that this extract was toxic to the larvae of the yellow fever mosquito, an insect that spreads a number of diseases. On the other hand it was found that the extract was harmless to rats. The authors conclude that the seeds and their extract could be used in mosquito control programs. According to Michael Lea (Jal Mandir Technology Clearinghouse) in an e-conference organized by USAID, quote: “Moringa oil on a water tank will help kill mosquito larvae and thus reduce the threat of malaria and other deadly insect-borne diseases.”

ABSTRACT

"Anais da Academia Brasileira de Ciencias"

In this work, biological effects of the water extract of Moringa oleifera seeds (WEMOS) were assessed on eggs and 3^rd instar larvae of Aedes aegypti and on its toxicity upon laboratory animals (Daphnia magna, mice and rats). Crude WEMOS showed a LC₅₀ value of 1260µg/mL, causing 99.2 ± 2.9% larvae mortality within 24 h at 5200µg/mL, though this larvicidal activity has been lost completely at 80ºC/10 min. WEMOS did not demonstrate capacity to prevent egg hatching. After extensive dialyses of the crude WEMOS into watersoluble dialyzable (DF) and nondyalizable (NDF) fractions, only DF maintained its efficacy to kill larvae. Acute toxicity evaluations on daphnids (EC₅₀ of 188.7µg/mL) and mice (LD₅₀ of 446.5 mg/kg body weight) pointed out to low toxicity. Despite the thymus hypertrophy, WEMOS revealed to be harmless in orally and subacutelytreated rats. In conclusion, WEMOS has thermostable bioactive compounds against Ae. aegypti larvae with apparent molecular mass lower than 12 kDa and moderately toxic potential.