Fortification of Carica papaya fruit seeds to school meal snacks may aid Africa mass deworming programs: a preliminary survey

M Kugo, L Keter, A Maiyo, J Kinyua, P Ndemwa, G Maina, P Otieno, E M Songok, M Kugo, L Keter, A Maiyo, J Kinyua, P Ndemwa, G Maina, P Otieno, E M Songok

Abstract

Background: Soil transmitted helminths (STHs) are among the world's neglected tropical diseases. Morbidity due to STHs is greatest in school-age children who typically have the highest burden of infection. In 2001, WHO passed a resolution for the use of large-scale mass drug administration (MDA) to deworm vulnerable children through school based programs. Though effective, there is concern that MDA might not be sustainable over extended periods. Additionally the current MDA strategy does not consider child malnutrition, a very common malady in resource limited countries. We report a pilot evaluation of an innovation that bundles school feeding and deworming.

Methods: We designed a maize (corn) flour fortified with grounded dried papaya (Carica papaya) seeds and used it to prepare porridge as per the usual school meal recipe Children from three primary schools from Nandi County in Kenya were randomized into three arms: One school received 300 ml papaya fortified porridge daily (papaya group), the second school received similar serving of plain porridge without the pawpaw ingredient (control group) and the third school received plain porridge and the conventional MDA approach of one time 400 mg dosage of albendazole (albendazole arm). Prior to the randomization, an initial baseline stool microscopy analysis was done to determine presence and intensity of intestinal worms. Core indicators of nutrition-height, weight and hemoglobin counts were also assessed. The children were monitored daily for two months and final stool sample analysis and clinical monitoring done at the end of the study. Baseline and follow-up data were analyzed and compared through SAS version 9.1 statistical package.

Results: A total of 326 children participated in the trial. The overall prevalence of Ascaris lumbricoides was 29.4% (96), Trichuris Trichura 5.2% (17) and hookworm 1 (0.3%). Papaya seed fortified porridge reduced the Ascaris lumbricoides egg count by 63.9% after the two month period (mean 209.7epg to 75.7 p < 0.002) as compared to the albendazole arm 78.8% (129.5 epg to 27.5, p value 0.006). The control group showed an increase in egg count (42.epg to 56.3) though it was not statistically significant. Hemoglobin counts in the papaya group increased from a mean of 2 g/dL (11.5 g/dL to 13.5 g/dL, p < 0.001), as compared to the albendazole arm that increased by 1 g/dL (12.8-13.9, p < 0.001). No significant change was observed in the placebo arm (13.2 to 13.1). Interestingly the papaya group showed a significant reduction of children with Tinea capitis (ringworms) (54.4 to 34%, p < 0.002) as compared to the albendazole arm that showed an increase in ringworm infestation though not statistically significant (39.7 to 64.7% p = 0.608).

Conclusion: Papaya seed fortified porridge had a significant effect on reduction of Ascaris lumbricoides burden. It had a better nutritional outcome and effect on child fungal infections than albendazole. Its application as a routine school meal may aid current national school based nutrition and deworming programs in Africa.

Trial registration: This study was retrospectively registered at Clinicaltrials.gov Ref. NCT02725255 on 31st March 2016.

Keywords: Africa; Albendazole; Carica papaya; Child nutrition; Helminths; Mass drug administration; Porridge; Ringworms; School children.

Conflict of interest statement

Ethics approval and consent to participate

The study was approved by the Kenya Medical Research Institute, Ethical Review Committee on 18th June13, 2013 (Ref KEMRI SSC 2580) and an annual renewal sought and approved on 16th September 2014 until July 2016. Written informed consent for the study and ensuring dissemination of the study results was received from all parents and guardians of participating children.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures

Fig. 1
Fig. 1
The flow chart summary of the study design

References

    1. WHO . Control of tropical disease. Geneva: world health organization; 1998. p. 201.
    1. Crompton DW. Ascaris lumbricoides. In: Scott ME, Smith G, editors. Parasitic and infectious diseases. London and New York: Academic Press; 1994. pp. 175–196.
    1. Oberhelman RA, Guerrero ES, Fernandez ML, Silio M, Mercado D, Comiskey N, et al. Correlations between intestinal parasitosis, physical growth, and psychomotor development among infants and children from rural Nicaragua. Am J Trop Med Hyg. 1998;58:470–475. doi: 10.4269/ajtmh.1998.58.470.
    1. Le HT, Brouwer ID, Verhoef H, Nguyen KC, Kok FJ. Anemia and intestinal parasite infection in school children in rural Vietnam. Asia Pac J Clin Nutr. 2007;16:716–723.
    1. Hall A, Hewitt G, Tuffrey V, de Silva N. A review and meta-analysis of the impact of intestinal worms on child growth and nutrition. Matern Child Nutr. 2008;4(Suppl 1):118–236. doi: 10.1111/j.1740-8709.2007.00127.x.
    1. Albonico M, Allen H, Chitsulo L, Engels D, Gabrielli AF, Savioli L. Controlling soil-transmitted helminthiasis in preschool-age children through preventive chemotherapy. PLoS Negl Trop Dis. 2008;2:e126. doi: 10.1371/journal.pntd.0000126.
    1. Dent JA, Smith MM, Vassilatis DK, Avery L. The genetics of ivermectin resistance in Caenorhabditis elegans. Proceedings of the National Academy of Sciences U S A. 2000;97:2674–2679. doi: 10.1073/pnas.97.6.2674.
    1. Williamson SM, Robertson AP, Brown L, Williams T, Woods DJ, Martin RJ, et al. The nicotinic acetylcholine receptors of the parasitic nematode Ascaris suum: formation of two distinct drug targets by varying the relative expression levels of two subunits. PLoS Pathog. 2009;5:e1000517. doi: 10.1371/journal.ppat.1000517.
    1. Abou Shady OM, Basyoni MM, Mahdy OA, Bocktor NZ. The effect of preziquantel and Carica papaya seeds on hymenolepis nana infection in mice using scanning electron microscope. Parasitol Res. 2014;113:2827–2836. doi: 10.1007/s00436-014-3943-4.
    1. Robinson, P., Seeds of Carica papaya for mass treatment against Ascariasis. Indian Journal of Child Health, 1958. I 7, : p. 815–817.
    1. Fernando PVD. Preliminary investigation of Carica papaya seeds as a vermifuge. Indian Journal of Child Health. 1959;8:96–100.
    1. Krishnakumari MK. Studies on anthelmintic activities of seeds of Carica papaya Linn. Annals of Biochemistry and Experimental Medicine. 1960;20:551–556.
    1. Kermanshai R, McCarry BE, Rosenfeld J, Summers PS, Weretilnyk E, Sorger GJ. Benzyl isothiocyanate is the chief or sole anthelmintic in papaya seed extracts. Phytochemistry. 2001;57:427–435. doi: 10.1016/S0031-9422(01)00077-2.
    1. Okeniyi JA, Ogunlensi AT, Oyelami AO, Adeyemi AL. Effectiveness of dried Carica papaya seeds against human intestinal parasitosis: a pilot study. J Med Food. 2007;10:194–196. doi: 10.1089/jmf.2005.065.
    1. Speich B, Ali SM, et al. Quality control in the diagnosis of Trichuris trichiura and Ascaris lumbricoides using the Kato-Katz technique: experience from three randomised controlled trials. Parasit Vectors. 2015;8(8):82. doi: 10.1186/s13071-015-0702-z.
    1. World Food Program (WFP). Fill the cup: turning hunger into hope for millions of children .
    1. Kwena AM, Terlouw DJ, de Vlas SJ, Phillips-Howard PA, Hawley WA, Friedman JF, et al. Prevalence and severity of malnutrition in pre-school children in a rural area of western Kenya. Am J Trop Med Hyg. 2003;68(4 Suppl):94–99. doi: 10.4269/ajtmh.2003.68.94.
    1. Suchdev PS, Davis SM, Bartoces M, Ruth LJ, Worrell CM, Kanyi H, et al. Soil-transmitted helminth infection and nutritional status among urban slum children in Kenya. Am J Trop Med Hyg. 2014;90:299–305. doi: 10.4269/ajtmh.13-0560.
    1. Nichto M, Geissler PW, Mubila L, Friis H, Oslen A. The effect of iron and multi micronutrient supplementation on Ascaris lumbricoides reinfection among Zambian schoolchildren. Trans R Soc Trop Med Hyg. 2009;103:229–236. doi: 10.1016/j.trstmh.2008.08.005.
    1. Tran T, Pattanee W, Marjoleine A, Nguyen C, Emorn W, Frank T. Decreased parasite load and improved cognitive outcomes caused by deworming and consumption of multi-micronutrient fortified biscuits in rural Vietnamese schoolchildren. Am J Trop Med Hyg. 2011;85:333–340. doi: 10.4269/ajtmh.2011.10-0651.
    1. Awasthi S, Peto R, Read S, Richards SM, Pande V, Bundy D. DEVTA (deworming and enhanced vitamin a) team population deworming every 6 months with albendazole in 1 million pre-school children in North India: DEVTA, a cluster-randomised trial. Lancet. 2013;381:1478–1486. doi: 10.1016/S0140-6736(12)62126-6.
    1. Taylor-Robinson DC, Maayan N, Soares-Weiser K, Donegan S, Garner P. Deworming drugs for soil-transmitted intestinal worms in children: effects on nutritional indicators. hemoglobin and school performance Cochrane Database Syst Rev. 2012;7:CD000371.
    1. Gordani R, Cardenas ML, Moulin-Traffort J, Régli P. Fungicidal activity of latex sap from Carica papaya and antifungal effect of D+glucosamine on candida albicans growth. Mycoses. 1996;39:103–110. doi: 10.1111/j.1439-0507.1996.tb00110.x.
    1. Bautista-Baños S, Barrera-Necha LL, Bravo-Luna I, Bermudes-Torres L. Antifungal activity of leaf and stem extracts from various plant species on the incidence of Colletotrichum gloesporoides of papaya and mango fruit after storage. Rev Mex Fitopatol. 2002;20:8–12.
    1. Singh O, Ali M. Phytochemical and antifungal profiles of the seeds of Carica papaya L. Indian J Pharm Sci. 2011;73:447. doi: 10.4103/0250-474X.99019.
    1. Sapaat A, Satrija F, Mahsol HH, Ahmad AH. Antihelminthic activity of papaya seeds on Hymenolepis diminuta infections in rats. Trop Biomed. 2012;29:508.

Source: PubMed

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