Molecular Characterization of SCRBQ2 Gene in Anopheles stephensi from Pakistan and Its Expression Dynamics After Blood Feeding: Implications for Malaria Transmission Control

Authors

  • Maria Department of Molecular Biology and Genetics, University of the Punjab, Lahore, Pakistan Author
  • Sana Shabana Department of Chemistry, Shaheed Benazir Bhutto Women University, Peshawar, KP, Pakistan. Author
  • Nazish Department of Molecular Biology and Genetics, University of the Punjab, Lahore, Pakistan Author

DOI:

https://doi.org/10.65761/jbs.v2.i1.6

Keywords:

Anopheles stephensi, SCRBQ2, Malaria transmission, Midgut receptor, Blood-feeding

Abstract

Background: Malaria remains a major public health challenge in Pakistan, with Anopheles stephensi serving as a primary urban vector. The croquemort-scavenger receptor class B2 (SCRBQ2) has been implicated in mediating Plasmodium invasion of the mosquito midgut and is considered a potential target for transmission-blocking strategies.

Objective: This study aimed to molecularly characterize the scrbq2 gene in A. stephensi from Karachi, Pakistan, and to investigate its tissue-specific and post-blood-meal expression dynamics.

Methods: A. stephensi adults (n = 335) were sampled and dissected to obtain midgut, fat body, salivary glands and ovaries. Ampification, sequencing, and submissions of the scrbq2 gene to GenBank (Accession ID: ON927345). In silico cloning and codon optimization were done to determine the potential of recombinant expression. Tissue-specific and temporal expression and changes during 0, 12, 26, 50, and 72 hours after blood meal (PBM) were determined by quantitative RT-PCR.

Findings: The scrbq2 gene has a 3068 bp coding sequence for a protein of 1022-amino-acid size with two fused CD36 competencies. A phylogenetic study showed great conservation among Anopheles species. The analysis of expression showed that the midgut was the most highly expressed followed by fat body, salivary glands and ovaries. The highest expression after blood meal was at 26 h PBM in the midgut and 50 h PBM in the fat body, which suggests a contribution to blood digestion and immune regulation.

Conclusion: The conserved domain architecture and dynamic expression of AsSCRBQ2 enables the consideration of this protein as an aspect of Plasmodium transmission alongside mosquito immunity. The results form the basis of the SCRBQ2-specific antiprequency interventions in Pakistan

References

Oladipo, H. J., Tajudeen, Y. A., Oladunjoye, I. O., Yusuff, S. I., Yusuf, R. O., Oluwaseyi, E. M., ... & El-Sherbini, M. S. (2022). Increasing challenges of malaria control in sub-Saharan Africa: Priorities for public health research and policymakers. Annals of Medicine and Surgery, 81, 104366.

Kolawole, E. O., Ayeni, E. T., Abolade, S. A., Ugwu, S. E., Awoyinka, T. B., Ofeh, A. S., & Okolo, B. O. (2023). Malaria endemicity in Sub-Saharan Africa: Past and present issues in public health. Microbes and Infectious Diseases, 4(1), 242–251.

Savi, M. K. (2022). An overview of malaria transmission mechanisms, control, and modeling. Medical Sciences, 11(1), 3.

Rogers, K. J., Vijay, R., & Butler, N. S. (2021). Anti-malarial humoral immunity: The long and short of it. Microbes and Infection, 23(4–5), 104807.

Hixson, B., Taracena, M. L., & Buchon, N. (2021). Midgut epithelial dynamics are central to mosquitoes’ physiology and fitness, and to the transmission of vector-borne disease. Frontiers in Cellular and Infection Microbiology, 11, 653156.

Hajkazemian, M., Bossé, C., Mozūraitis, R., & Emami, S. N. (2021). Battleground midgut: The cost to the mosquito for hosting the malaria parasite. Biology of the Cell, 113(2), 79–94.

Lewis, J., Gallichotte, E. N., Randall, J., Glass, A., Foy, B. D., Ebel, G. D., & Kading, R. C. (2023). Intrinsic factors driving mosquito vector competence and viral evolution: A review. Frontiers in Cellular and Infection Microbiology, 13, 1330600.

Suh, P. F., Elanga-Ndille, E., Tchouakui, M., Sandeu, M. M., Tagne, D., Wondji, C., & Ndo, C. (2023). Impact of insecticide resistance on malaria vector competence: A literature review. Malaria Journal, 22(1), 19.

Baia-Silva, D. C., Monteiro, W. M., de Lacerda, M. V. G., Secundino, N. F. C., & Pimenta, P. F. P. (2022). Cellular and molecular interactions of Plasmodium with mosquito vectors. In Lifecycles of pathogenic protists in humans (pp. 283–329). Cham: Springer International Publishing.

Keleta, Y., Ramelow, J., Cui, L., & Li, J. (2021). Molecular interactions between parasite and mosquito during midgut invasion as targets to block malaria transmission. npj Vaccines, 6(1), 140.

Ouologuem, D. T., Dara, A., Kone, A., Ouattara, A., & Djimde, A. A. (2023). Plasmodium falciparum development from gametocyte to oocyst: Insight from functional studies. Microorganisms, 11(8), 1966.

Yu, S., Wang, J., Luo, X., Zheng, H., Wang, L., Yang, X., & Wang, Y. (2022). Transmission-blocking strategies against malaria parasites during their mosquito stages. Frontiers in Cellular and Infection Microbiology, 12, 820650.

Parres-Mercader, M., Pance, A., & Gómez-Díaz, E. (2023). Novel systems to study vector-pathogen interactions in malaria. Frontiers in Cellular and Infection Microbiology, 13, 1146030.

Bachmann, A., Metwally, N. G., Allweier, J., Cronshagen, J., del Pilar Martinez Tauler, M., Murk, A., ... & Bruchhaus, I. (2022). CD36—A host receptor necessary for malaria parasites to establish and maintain infection. Microorganisms, 10(12), 2356.

Oleinikov, A. V. (2022). Malaria parasite Plasmodium falciparum proteins on the surface of infected erythrocytes as targets for novel drug discovery. Biochemistry (Moscow), 87(Suppl 1), S192–S202.

Jensen, A. R., Adams, Y., & Hviid, L. (2020). Cerebral Plasmodium falciparum malaria: The role of PfEMP1 in its pathogenesis and immunity, and PfEMP1‐based vaccines to prevent it. Immunological Reviews, 293(1), 230–252.

Petersen, J. E., Saelens, J. W., Freedman, E., Turner, L., Lavstsen, T., Fairhurst, R. M., ... & Taylor, S. M. (2021). Sickle-trait hemoglobin reduces adhesion to both CD36 and EPCR by Plasmodium falciparum-infected erythrocytes. PLoS Pathogens, 17(6), e1009659.

Fraser, M., Matuschewski, K., & Maier, A. G. (2021). Of membranes and malaria: Phospholipid asymmetry in Plasmodium falciparum-infected red blood cells. Cellular and Molecular Life Sciences, 78(10), 4545–4561.

Bonam, S. R., Rénia, L., Tadepalli, G., Bayry, J., & Kumar, H. M. S. (2021). Plasmodium falciparum malaria vaccines and vaccine adjuvants. Vaccines, 9(10), 1072.

Ferdous, Z., & Uddin, M. H. (2023). Mosquito defense mechanisms against medically important arboviruses: The vector-pathogen interface. In Viral, Parasitic, Bacterial, and Fungal Infections (pp. 151–159). Academic Press.

Zeng, T., Jaffar, S., Xu, Y., & Qi, Y. (2022). The intestinal immune defense system in insects. International Journal of Molecular Sciences, 23(23), 15132.

Maitre, A., Wu-Chuang, A., Aželytė, J., Palinauskas, V., Mateos-Hernández, L., Obregon, D., ... & Cabezas-Cruz, A. (2022). Vector microbiota manipulation by host antibodies: The forgotten strategy to develop transmission-blocking vaccines. Parasites & Vectors, 15(1), 4.

Dong, S., & Dimopoulos, G. (2021). Antiviral compounds for blocking arboviral transmission in mosquitoes. Viruses, 13(1), 108.

Marín-López, A., Raduwan, H., Chen, T. Y., Utrilla-Trigo, S., Wolfhard, D. P., & Fikrig, E. (2023). Mosquito salivary proteins and arbovirus infection: From viral enhancers to potential targets for vaccines. Pathogens, 12(3), 371.

Prince, B. C., Walsh, E., Torres, T. Z. B., & Rückert, C. (2023). Recognition of arboviruses by the mosquito immune system. Biomolecules, 13(7), 1159.

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Published

2025-06-30

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Section

Original Research Article

How to Cite

Maria, Shabana, S., & Nazish. (2025). Molecular Characterization of SCRBQ2 Gene in Anopheles stephensi from Pakistan and Its Expression Dynamics After Blood Feeding: Implications for Malaria Transmission Control. Journal of Bioscience Studies, 2(1), 1-4. https://doi.org/10.65761/jbs.v2.i1.6

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