Mosquito Species Composition in Nasarawa Local Government, Nasarawa State, Nigeria

Authors

  • Akwashiki Ombugadu Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria
  • Saleh Usman Muhammed Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria
  • James I Maikenti Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria
  • Abdullahi Abubakar Ali Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria https://orcid.org/0009-0008-3090-6010
  • Mohammed A Ashigar Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria
  • Hussein O Ahmed Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria
  • Sunday Igboanugo PMI Evolved project Nigeria ABT Associates, Nigeria & Department of Zoology, University of Jos, PMB 2084, Jos, Plateau State Nigeria
  • Grace I Yina Department of Zoology, Nasarawa State University Keffi, Nasarawa State, Nigeria
  • Victoria A Pam Department of Zoology, Faculty of Science, Federal University of Lafia, P. M. B. 146, Lafia, Nasarawa State, Nigeria

DOI:

https://doi.org/10.56919/usci.2434.005

Keywords:

Mosquito, Composition, Nasarawa LGA

Abstract

Study’s Excerpt

  • The resting densities, biting rates, and indoor mosquito populations in Nasarawa LGA were assessed.
  • Prokopack aspirator is applied for morning mosquito collection and the dissecting microscope for identification of species-specific attributes.
  • The results highlight critical areas for targeted vector control to mitigate malaria transmission in the region.

Full Abstract

Numerous mosquito species are capable of carrying various tropical diseases.  This study ascertained the composition of mosquitoes in Nasarawa Local Government Area.  Adult mosquitoes were collected between 0600 and 0900 hours in the morning using a battery-operated Prokopack aspirator.  The mosquitoes were then placed in a petri dish with proper labelling and taken to a laboratory for identification and dissection.  Using a dissecting microscope and identification key, mosquitoes were sorted and morphologically classified according to their morphological features.  The mosquito midgut was dissected to check for sporozoites infectivity.  The man-biting rate (MBR) and indoor resting density (IRD) were computed.  A total of 314 adult mosquitoes, spanning four species and belonging to the Anopheline and Culicine mosquito groups, were found to be resting indoors with An. gambiae representing 39.2% of the total composition.  A significant difference in mosquito abundance (χ2= 58.866, df = 3, P=0.001) was observed between the four species that were reported.  There is no discernible variation in the mosquito composition in the research region (χ2= 4.861, df = 2, P = 0.088).  A statistically significant variance in sex was noted (χ2=285.235, df = 2, P = 0.000).  The biting rate was recorded at 2.6 bites per person per night, and an indoor resting density of 5.23 mosquitoes per room per night was recorded.  There was a noteworthy distinction in the abdomen condition of the mosquitoes (χ2 = 45.564, df = 3, p < 0.001).  Mosquito species abundance in October was 200 (63.7%), compared to 114 (36.3) in September.  Nonetheless, a noteworthy distinction was observed in the abundance of mosquito species throughout the research months (χ2= 7.5076, df = 1, P-value = 0.006).  Because the study's findings provided insight into the species composition of the mosquito population in the study area, it is recommended to remove possible breeding grounds, promote the use of insecticide-treated nets, and prioritize interrupting vector-human contact as a means of halting the spread of malaria parasites.

References

Abeku, T. A., Helinski, M. E., Kirby, M. J., Kefyalew, T., Awano, T., Batisso, E., Tesfaye, G., Ssekitooleko, J., Nicholas, S., Erdmanis, L., & Meek, S. R. (2015). Monitoring changes in malaria epidemiology and effectiveness of interventions in Ethiopia and Uganda: beyond Garki project baseline survey. Malaria Journal, 14, Article number 337. https://doi.org/10.1186/s12936-015-0852-7

Adeleke, M. A., Mafiana, C. F. & Idowu, O. A. (2010). Population Dynamics of indoor sampled mosquitoes and their implication in disease transmission in Abeokuta, south-western Nigeria. Journal of Vector Borne Disease 47(1): 33-38.

Adeoye, G. O., Edeh, I. C., Olayiwola, O. A., Ayodele, E. T. & Adeleke, M. A. (2012). The abundance and composition of endophilic mosquito in the University of Lagos and its Environment. Nigeria Journal of Parasitology, 33(1): 21-25.

Agidi, V. A., Hassan, S. M., & Baleri, T. G. (2017). Trends in staple crop yields in Nasarawa State, Nigeria. Agricultural Studies, 2(4), 153-161.

Braack, L., Hunt, R., Koekemoer, L. L., Gericke, A., Munhenga, G., Haddow, A. D., Becker, P., Okia, M., Kimera, I. & Coetzee, M. (2015). Biting behaviour of African malaria vectors: 1. where do the main vector species bite on the human body? Parasites & Vectors, 8, Article number 76. https://doi.org/10.1186/s13071-015-0677-9

Buttachon, S.; Arikit, S.; Nuchchanart, W.; & Puangmalee, T. (2022) Geometric Morphometric Analysis and Molecular Identification of mosquitoes 2022, 13, 102. https://doi.org/10.3390/insects13111022

Coetzee, M. (2020). Key to the female of Afrotropical Anopheles mosquitoes (Diptera: Culicidae). Malaria journal, 19, 70. https://doi.org/10.1186/s12936-020-3144-9

Dogara, M., Nock, H., Agbede, R., Ndams, S., & Joseph, K. (2012). Entomological survey of mosquitoes responsible for the transmission of lymphatic filariasis in three endemic villages of Kano state, Nigeria. The Internet Journal of World Health and Societal Politics, 7(2), 1-6. https://doi.org/10.5580/2b44

Ebenezer A, Ben HIB, Enaregha EB (2013) Atial distribution and indoor resting density of mosquito species in the lowland rainforest of Bayelsa State, Nigeria. International Journal of Tropical Medicine 8(4): 87-91.

Ezeigwe, N., Inyama, P.U., Samdi, L.M., Akila, J.D., Awolola, T.S., Mwansat, G.S., Anyawu, G.I., Yayo, A.M., Ebere, N., Chukwuekezie, O., Seyuom, A., Inyang, U., Kafuko, J., Kolyada, L., Fornadel, C. & Norris, L. (2015). Anopheles Species Diversity, Behaviour, and Sporozoite Rates in Six States of Nigeria. American Journal of Tropical Medicine and Hygiene, 93(4), 425-425.

Ezihe, E. K., Egbuche, C. M., Nwankwo, E. N., Ukonze, C., Anumba, J. U., Umenzekwe, C. C., & Ogudu, O. E. (2019). Malaria vector abundance and the incidence of malaria parasite amongst students living in nnamdi azikiwe university hostels. International Journal of Tropical Disease and Health, 37(4), 1-10. https://doi.org/10.9734/ijtdh/2019/v37i430169

Flies, E.J., Flies, A.S., Fricker, S.R., Weinstein, P. and Williams, C.R. (2016). Regional Comparison of Mosquito Bloodmeals in South Australia: Implications for Ross River Virus Ecology. Journal Medical Entomology.53:902–10. https://doi.org/10.1093/jme/tjw035

Franklinos, L. H. V., Jones, K. E. & Redding, D. W. (2019). The effect of global change on mosquito-borne disease. Lancet Infectious Disease, 19(9), e302–e312. https://doi.org/10.1016/S1473-3099(19)30161-6

Goupeyou-Youmsi, J., Rakotondranaivo, T., Puchot, N., Peterson, I., Girod, R., Vigan-Womas, I., Paul, R., Ndiath, M. O., & Bourgouin, C. (2020). Differential contribution of Anopheles coustani and Anopheles arabiensis to the transmission of Plasmodium falciparum and Plasmodium vivax in two neighbouring villages of Madagascar. Journal of Parasites & Vectors, 13, Article number 430. https://doi.org/10.1186/s13071-020-04282-0

Howell, P. I., & Chadee, D. D. (2007). The influence of house construction on the indoor abundance of mosquitoes. Journal of Vector Ecology, 32(1), 69-74. https://doi.org/10.3376/1081-1710(2007)32[69:TIOHCO]2.0.CO;2

Kilama, W. L. (2010). Health research ethics in malaria vector trials in Africa. Malaria Journal, 9, Article number S3. https://doi.org/10.1186/1475-2875-9-S3-S3

Madara AA, Abdulraheem NO, Elkanah SO (2013) Relative Abundance of Adult Mosquitoes in University of Abuja Main Campus, Abuja FCT, Nigeria. Nigerian Journal of Parasitology 34(2): 79-84.

Manguin, S.; Bangs, M.J.; Pothikasikorn, J. and Chareonviriyaphap, T. (2009). Rewiew on global co-transmission of human Plasmodium species and Wuchereria bancrofti by Anopheles mosquitoes. Infection, Genetics and Evolution, 10(2010): 159-177. https://doi.org/10.1016/j.meegid.2009.11.014

Manzoor, F., Shabbir, R.,Sana, M.,Nazir, S., & Aslam Khan, M. (2020).Determination of Species Composition of Mosquitoes in Lahore, Pakistan. Journal of Arthropod-Borne Diseases, 14(1), 106-115. https://doi.org/10.18502/jad.v14i1.2717

Ménard, D., Barnadas, C., Bouchier, C., & Henry-Halldin, C. (2013). Plasmodium vivax clinical malaria is commonly observed in Duffy-negative Malagasy people. Proceedings of the National Academy of Sciences, 107(13), 5967-5971. https://doi.org/10.1073/pnas.0912496107

Msugh-Ter MM, Mngurumun AL, Emmanuel OI (2017) Personal Protective Practices Against Mosquito Bites by Undergraduate Students of Federal University of Agriculture Makurdi, North Central Nigeria. American Journal of Entomology 1(2): 27-30.

NAGIS (2024). Nasarawa State Geographic Information Service, Nagis. Map of Nasarawa LGA.

Njila, H. L., Ngwa, I. K., Bilham, I. Y. and Ombugadu, A. (2022). Infection Status of Mosquitoes in Kunga Community of Jos North Local Government Area, Plateau State, Nigeria. Nigerian Journal of Parasitology 43(2) 385-391. https://doi.org/10.4314/njpar.v43i2.22

Okorie, P. N., Popoola, K. O. K., Awobifa, O. M., Ibrahim, K. T., & Ademowo, G. O. (2014). Species composition and temporal distribution of mosquito populations in Ibadan, Southwest Nigeria. Journal of Entomology and Zoology Studies, 2(4), 164-169.

Okwa, O. O., Rasheed, A., Adeyemi, A., Omoyeni, M. & Oni, L. (2007). Anopheles species abundance, composition and vectoral competence in six areas of Lagos, Nigeria. Journal of Cell and Animal Biology 1(2): 15 23.

Okwa, O. O. & Sulaimon, R. (2004). Dynamics of the transmission of Malaria in Ojo Local Government Area of Lagos Nigeria. Journal of Research and Review in Science 3: 16.

Ombugadu, A., Jibril, A. B., Mwansat, G. S., Njila, H. L., Attah, A. S., Pam, V. A., Benson, R. F., Maikenti, J. I., Deme, G. G., Echor, B. O., & Nkup, C. D. (2022). Composition and Distribution of Mosquito Vectors in a Peri-Urban Community Surrounding an Institution of Learning in Lafia Metropolis, Nasarawa State, Central Nigeria. Journal of Zoological Research, 4(3), 20-31. https://doi.org/10.26717/BJSTR.2020.28.004691

Ombugadu, A., Maikenti, J. I., Maro, S. A., Vincent, S. O., Polycarp, I. A., Pam, V. A., Samuel, M.D., Adejoh, V. A., Attah, A. S., Ahmed, H. O., & Angbalaga, G. A. (2020). Survey of mosquitoes in students hostels of Federal University of Lafia, Nasarawa State, Nigeria. Biomedical Journal of Scientific & Technical Research, 28(4), 21822-21830.

Onyango, S.A.; Kitron, U.; Mungai, P.; Muchiri, E.M.; Kokwaro, E.; King, C.H. and Mutuku, F.M. (2013). Monitoring malaria vector control interventions: effectiveness of five different adult mosquito sampling methods. Journals of Medical Entomology50(5): 1140-1151. https://doi.org/10.1603/ME12206

Onyido, A. E., Deezia, N. P. L., Obiukwu, M., & Amadi, E. (2008). Ecology of man-biting mosquitoes in the development site of Nnamdi Azikiwe University Awka, Anambra State South Eastern Nigeria. The Internet Journal of Health, 9(2), 1-7. https://doi.org/10.5580/69e

Osidoma, E. O.1, Pam, V. A.1, Uzoigwe, N. R.1, Ombugadu, A.1, Omalu, I. C. J.2, Maikenti, J. I.1, Attah, A. S.1, Ashigar, M. A.1 and Dogo, S. K. (2023). A study on mosquitoes composition and malaria transmission in some communities in Doma Local Government Area of Nasarawa State, Nigeria. Journal of Bioscience and Biotechnology Discovery. 8(1): 10-17. https://doi.org/10.31248/JBBD2023.176

Oyewole, I.O., Awolola, T.S., Ibidapo, C.A., Okwa, O.O. and Obansa, J.A Paaijmans, K. P., Read, AF.and Thomas, M. B. (2009). Understanding the link between malaria risk and climate. Plant National Academic Science USA 106: 13844–13849. https://doi.org/10.1073/pnas.0903423106

World Health Organization. (2019). The world health report 2004 – changing history.

World Health Organization. (2016). Vector-Borne Diseases. Fact Sheet -WHO. (2019) World Malaria Report pp. 232.

WHO (2020). West Nile virus. Geneva. Available from: www.who.int/news-room/fact-sheet/details/West Nile virus

Williams, J. and Pinto, J. (2012). Training Manual on Malaria Entomology for Entomology and Vector Control Technicians (Basic Level). Integrated Vector Management of Malaria and Other Infectious Diseases Task Order 2Contract GHA-I-02-04-00007-00United States Agency for International Development.

Yoriyo, K. P., Alo, E. B., Napthali, R. S., Pukuma, S. M., Edward, S. A., & Muhammad, I. (2013). A quantitative study on the population of indoor resting density of mosquito species in four Local Government Areas of Gombe State, Nigeria. Journal of Medical and Biological Sciences, 3(1), 61-67.

Downloads

Published

2024-10-14

How to Cite

Ombugadu, A., Muhammed, S. U., Maikenti, J. I., Ali , A. A., Ashigar, M. A., Ahmed, H. O., Igboanugo, S., Yina, G. I., & Pam, V. A. (2024). Mosquito Species Composition in Nasarawa Local Government, Nasarawa State, Nigeria. UMYU Scientifica, 3(4), 46–56. https://doi.org/10.56919/usci.2434.005

Most read articles by the same author(s)