Assessing the Entomological Parameters of Malaria Vectors in Anambra State, Southeast Nigeria
Asian Journal of Research in Zoology, Volume 6, Issue 3,
Page 1-15
DOI:
10.9734/ajriz/2023/v6i3111
Abstract
Adequate knowledge of entomological parameters within a defined geographic endemic area is basic for effective planning of malaria vector control for malaria elimination. The study investigated sibling species of malaria vectors, indoor resting density (IRD), human biting rate (HBR), blood meal source (BMS), human blood index (HBI), sporozoite rate (SR) and entomological inoculation rate (EIR) of malaria vectors in Awka North, Awka South and Njikoka Local Government Areas in Anambra State, southeast Nigeria. Pyrethrum spray collection (PSC), Centre for Disease Control (CDC) light trap, and human landing catch (HLC) techniques were the methods used for collection of indoor and outdoor malaria vectors. Mosquitoes collected were sorted according to species and sex; and identified using standard morphological and molecular techniques. Chi-square test was used for data analysis. A total of 2,870 Anopheles mosquitoes were collected, male 1949 (67.9%) and female 921 (32.1%). All female species identified morphologically belong to the Anopheles gambiae s. l. complex. From the molecular and siblings species separation, Anopheles gambiae recorded the highest abundance of 54.2% and Anopheles coluzzii the least abundance of 45.8%. The IRD was found to be 1.40 per man per night with an average HBR of 5.05. The blood meal source showed that human blood source was the highest number with 46.2%, followed by goat blood source with 32.7%, and combination of human and goat blood was the least with 21.2%. The result also showed a HBI of 0.51 whereas the test for the presence of circumsporozoite protein (CSP) of Plasmodium falciparum shows that none of the malaria vectors was positive for sporozoite; thus, the EIR could not be determined and compared among the study population. The values of the entomological parameters and the allopatric breeding of the two sibling species of Anopheles gambiae and Anopheles coluzzii reported in this study which is probably the second of such report in Nigeria has a huge implications for malaria vector control and malaria control in Anambra State, Southeast Nigeria.
- Blood meal source
- entomological parameters
- malaria vectors
- Anambra State
How to Cite
References
Center for disease Control. Anopheles mosquitoes. Global Health Division of parasitic diseases and malaria; 2015.
Autino IJ, Andersen FS. The negative binomial distribution and the sampling of insect populations. Proceedings of the 12th International Congress of Entomology. 2012;395:395-399.
Gillies MT, Coetzee M. A supplement to the Anophelinea of Africa south of the Sahara (Afrotropical region). South African Institute for medical Research, Johannesburg. 1987;55:143.
Scott EB, Chareonviriyaphap T, Coetzee M, Mbogo CM. A global map of dominant malaria vectors. Parasitology Vectors. 1993;(5):69.
Kirby MJ, Green C, Milligan PM, Sismanidis C, Jasseh M, Conway DJ, Lindsay SW. Risk factors for house-entry by malaria vectors in a rural town and satellite villages in The Gambia. Malaria Journal 2018;7:2-10.
DOI: 10.1186/1475-2875-7-2
Smith D, Battle K, Hay S, Barker C, Scott T, McKenzie F. Ross, Macdonald, and a theory for the dynamics and control of mosquito-transmitted pathogens. Plos Pathogen. 2012;8:e1002588.DOI: 10.1371/journal.ppat.1002588.
Lindsay EB, Marbiah NT, Maude G, Curtis CF, Bradley DJ, Greenwood BM, Petersen E, Lines JD. Effects of community-wide use of lambdacyhalothrin-impregnated bednets on malaria vectors in rural Sierra Leone. Medical and Veterinary Entomology. 2018;11:79–86.
Onori OD, Conn JE. The Distribution of Two Major Malaria Vectors, Anopheles gambiae and Anopheles arabiensis, in Nigeria. Mem Inst Oswaldo Cruz, Rio de Janeiro. 2001;96(8):1081±1084.
Microsoft Encarta College Dictionary and Encyclopedia. New York: St. Martin’s Press. 2009:276.
Access on 23 March, 2020
National Bureau of Statistics. National Population Commission 2006 Nigeria Census; 2016.
Enete IC. Managing aviation operations during harmattan in Nigeria for maximum operations. Inpritx Lagos State, Nigeria. 2008:12-23.
Enete IC. A study of Enugu rainfall patterns from the viewpoint of precipitation dynamics. “Nigeria Journal of Research and Production”, Nigerian Researchers Forum Enugu. 2004;5(4):98-108.
National Population Commission. Nigerian Malaria Indicator Survey; Key Indicators survey in 2017. Descriptive Support System. 2016:1–37.
World Health Organization. Entomological field techniques for malaria control part I learners guide. World Health Organization, Geneva; 1992.
World Health Organization. Antimalarial drug resistance; 2015.
Available:http://www.who.int/malaria/areas/drug_resistance/overview/en/ Access on March 11, 2021).
Abdoon JK, Alshahrani S. Age-dependent acquired protection against Plasmodium falciparum in people having two years exposure to hyperendemic malaria. American Journal of Tropical Medicine and Hygiene. 2003;45:65-76.
Curtis WG. A distribution map of the member species of Anopheles gambiae complex. Transactions of the Royal Society of Tropical Medicine and Hygiene. 2003;61:454.
Gillies MT, Meillon DB. The Anophelinae of Africa South of the Sahara. Publications of the South African Institute for Medical Research. 1968;15:1-343.
Wilkins RU, Nicholas T, Fontenille D. Identification of mammalian blood meals in mosquitoes by a multiplexed polymerase chain reaction targeting cytochrome B. American Journal of Tropical Medicine and Hygiene. 2006;3:36–42
Keven JB, Michelle K, Rebecca V, Gussy K, Naomi V, Edward K, Thomsen SK, Lisa J, Reimer DW. Species abundance, composition, and nocturnal activity of female Anopheles (diptera: Culicidae) in malaria‑endemic villages of Papua New Guinea: Assessment with barrier screen sampling. Malaria Journal. 2019;18:96.
Dash AP, Hazra RK, Mahapatra N, Tripathy HK. Disappearance of malaria vector Anopheles sundaicus from Chilka lake area of Orissa state in India. Medical Veterinary and Ecology. 2000;14:445–449.
Kulkarni SM. Density pattern of anophelines and their relation to malaria in Bastar district, Madhya Pradesh. Journal of Malariology. 1990;27:187–194.
Sharma VP. Fighting malaria in India. Current Science. 1998;75:1127–1140.
Kulkarni SM. Density pattern of anophelines and their relation to malaria in Bastar district, Madhya Pradesh. Journal of Malariology. 2019;27:187–194.
Mahesh RK, Jauhari RK. Seasonal abundance of vector anophelines in Doiwala area of Doon Valley, Uttaranchal. Journal of Parasitology and Applied Animal Biology. 2004;13:65–70.
Krafsur CS. The bionomics and relative prevalence of Anopheles species with respect to the transmission of Plasmodium to man in western Ethiopia. Journal of Medical Entomology. 2017;14:180–94.
D’Acremont V, Lengeler C, Genton B. Reduction in the proportion of fevers associated with Plasmodium falciparum parasitaemia in Africa: A systematic review. Malaria Journal. 2010;9:240.
Mharakurwa S, Mutambu SI, Mberikunashe J, Thuma PE, Moss WJ, Mason PR. Changes in the burden of malaria following scale up of malaria control interventions in Mutasa District, Zimbabwe. Malaria Journal. 2013;12:223.
Mutuku FD, King CH, Mungai P, Mbogo C, Mwangangi J, Muchiri EM. Impact of insecticide-treated bed nets on malaria transmission indices on the south coast of Kenya. Malaria Journal. 2011;10:356.
Gimnig JE, Vulule JM, Lo TQ, Kamau L, Kolczak MS, Phillips-Howard PA. Impact of permethrin-treated bed nets on the entomologic indicies in an area of intense year-round malaria transmission. American Journal of Tropical Medicine and Hygiene. 2013;68:115–20.
World Health Organization. Control of residual malaria parasite transmission: Guidance note. WHO Geneva. 2014;12:222-267.
Mwangan EP, Salum A, Mapua DJ, Siria HS, Ngowo FN, Joseph M, Francesco B, Mario GJ, Heather M, Ferguson KW, Prashanth S, Simon AB, Fredros OO. Using mid‑infrared spectroscopy and supervised machine‑learning to identify vertebrate blood meals in the malaria vector, Anopheles arabiensis. Malaria Journal. 2019;18:187.
Kent WH, Norris SM. Density pattern of anophelines and their relation to malaria in Bastar district, Madhya Pradesh. Journal of Malariology. 2005;27:187–194.
Chow E, Wirtz RA, Scott TW. Identification of blood meals in Aedes aegypti by antibody sandwich enzyme-linked immunosorbent assay. Journal of American Mosquitoes Control Association. 1993;9:196–205.
World Health Organisation. Vector control for malaria and other mosquito-borne diseases. Technical Report. 2020:23-33.
Burkot TR, Dye C, Graves PM. An analysis of some factors determining the sporozoite rates, human blood indexes, and biting rates of members of the Anopheles punctulatus complex in Papua New Guinea. American Journal of Tropical Medicine and Hygiene. 1989;40:229–34.
Vasiliki P, Michael R, Hans J, Overgaard SA, Adalgisa C. Estimation of the human blood index in malaria mosquito vectors in equatorial Guinea after indoor antivector interventions. American Journal of Tropical Medicine and Hygiene. 2011;84(2):298–301. DOI: 10.4269/ajtmh.2011.10-0463
Muirhead-Thomson RC. Mosquito behaviour in relation to malaria transmission and control in the tropics. London: Edward Arnold & Co. 1957:56–70.
Sousa CA, Pinto J, Almeida AP, Ferreira C, do Rosario VE, Charlwood JD. Dogs as a favored host choice of Anopheles gambiae sensu stricto (diptera: Culicidae) of São Tomé West Africa. Journal of Medical Entomology. 2001;38:122–125.
Duchemin JB, Leongpocktsy JM, Rabarison P, Roux J, Coluzzi M, Costantini C. Zoophily of Anopheles arabiensis and An. gambiae in Madagascar demonstrated by odour-baited entry traps. Medical and Veterinary Entomology. 2001;15:50–57.
Teklehaimanot HD, Teklehaimanot A, Kiszewski A, Sacramento Rampao H, Sachs JD. Malaria in São Tomé and Principe: on the brink of elimination after 3 years of effective antimalarial measures. American Journal of Tropical Medicine and Hygiene. 2009;80:133–140.
Githeko AK, Service MW, Mbogo CM, Atieli FK, Juma FO. Origin of blood meals in indoor and outdoor resting malaria vectors in Western Kenya. Acta Tropica. 1994;58:307–316.
Okwa OO, Akinmolayan FI, Carter V, Hurd H. Transmission dynamics of malaria in four selected ecological zones of Nigeria in the rainy season. Annals of African Medicine. 2009;8:1–9.
Wanji S, Tanke T, Atanga SN, Ajonina C, Nicholas T, Fontenille D. Anopheles species of the mount Cameroon region: Biting habits, feeding behaviour and entomological inoculation rates. Tropical Medicine and International Health. 2003;8:643–649.
Tanga, MC, Ngundu WI, Judith N, Mbuh J, Tendongfor N, Simard F, Wanji S. Climate change and altitudinal structuring of malaria vectors in South-Western Cameroon: Their relation to malaria transmission. Transactions of Royal Society of Tropical Medicine and Hygiene. 2010;104:453–460.
Magbity EB, Marbiah NT, Maude G, Curtis CF, Bradley DJ, Greenwood BM, Petersen E, Lines JD. Effects of community-wide use of lambdacyhalothrin-impregnated bednets on malaria vectors in rural Sierra Leone. Medical and Veterinary Entomology. 1997;11:79–86.
Silver JB. Mosquito ecology: Field sampling methods. New York, Springer. 2018:372–492.
Ledayane MC, Barbosa RN, Picanc S, Ricardo S, Anjos F, Margarete S. Behavioral patterns, parity rate and natural infection analysis inanopheline species involved in the transmission of malaria in the northeastern Brazilian Amazon region. Acta Tropica. 2016;164:216–225.
Marco P, Maria C, Wamdaogo M, Guelbeogo MM, Eleonora P, Verena P, Emiliano M, N’Fale S, Hilary R, Alessandra della T. Unexpectedly high Plasmodium sporozoite rate associated with low human blood index in Anopheles coluzzii from a LLIN-protected village in Burkina Faso. Scientific Reports. 2018;8(2018):12806.
Koella Koekemoer LL, Spillings BL, Christian RN, Lo T-CM, Kaiser ML, Norton RAI. Multiple insecticide resistance in Anopheles gambiae (diptera: Culicidae) from Pointe Noire, Republic of the Congo. Vector Borne Zoonotic Diseases. 1998;11:1193–2000.
Nyasembe VO. Plasmodium falciparum infection increases Anopheles gambiae attraction to nectar sources and sugar uptake. Current Biology. 2014;24:217–21.
Smallegange RC. Malaria infected mosquitoes express enhanced attraction to human odor. Plos One. 2013;8:8–10.
Cator LJ. ‘Manipulation’ without the parasite: altered. Proceedings of Biological Sciences. 2013;65:73–78.
Autino B, Noris A, Russo R, Castelli F. Epidemiology of malaria in endemic areas. Meditter Journal Hematology Infectious Disease. 2012;4(1):60.
Onori E, Grab B. Indicators for the forecasting of malaria epidemics. Bull World Health Organization. 1980;58: 91-98.
World Health Organization. World malaria report, Geneva. 2016:280.
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