Mechanisms and targets of harnessing Culex pipiens-specific antibodies as a novel vector control strategy

Xuebin Zhao , Jian Zheng , Weimin Zheng , Jinrong Lin , Guangshuo Ding , Xinhui Yu , Jun Cao , Yun Chen , Bo Shen , Gaoqian Feng

Journal of Biomedical Research ›› 2026, Vol. 40 ›› Issue (2) : 159 -171.

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Journal of Biomedical Research ›› 2026, Vol. 40 ›› Issue (2) :159 -171. DOI: 10.7555/JBR.39.20250135
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Mechanisms and targets of harnessing Culex pipiens-specific antibodies as a novel vector control strategy
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Abstract

Mosquito-borne diseases pose a significant global health threat, necessitating the development of innovative vector control strategies. In this study, we investigated the potential of harnessing host immunity against mosquitoes through vaccination. Using Culex pipiens (C. pipiens) as a model, we demonstrated that polyclonal antibodies against C. pipiens abdominal protein extracts significantly impaired oviposition and increased mosquito mortality, primarily through the classical complement activation pathways. However, repeated exposure led to resistance, indicating potential adaptation. Proteomic analysis identified metabolic proteins as key targets, with Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses highlighting their roles in carboxylic acid metabolism, tyrosine degradation, and the proteasome pathways. Notably, cross-species reactivity was revealed by Western blotting, showing strong binding of Culex-specific antibodies to Anopheles and Aedes abdominal proteins. This study provides mechanistic insights into antibody-based mosquito suppression, highlighting its potential as an innovative vector control strategy while underscoring the need for further research on resistance management and ecological impacts.

Keywords

Culex / antibodies / classical complement pathway / oviposition / mosquito control

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Xuebin Zhao, Jian Zheng, Weimin Zheng, Jinrong Lin, Guangshuo Ding, Xinhui Yu, Jun Cao, Yun Chen, Bo Shen, Gaoqian Feng. Mechanisms and targets of harnessing Culex pipiens-specific antibodies as a novel vector control strategy. Journal of Biomedical Research, 2026, 40(2): 159-171 DOI:10.7555/JBR.39.20250135

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Funding

This work was supported by the National Natural Science Foundation of China (Grant No. 82472312).

Acknowledgments

We thank Dr. Guoding Zhu and Dr. Jianxia Tang of the Jiangsu Institute of Parasitic Diseases for providing technical support for the initial establishment of our insectary. We also thank Dr. Sean Lynch and Dr. Bridget Barber of QIMR Australia for sharing the mosquito membrane feeding assay methods, and Prof. Lin Chen of Nanjing Medical Univeristy for providing the Aedes aegypi.

References

[1]

Krambrich J, Akaberi D, Lindahl JF, et al. Vector competence of Swedish Culex pipiens mosquitoes for Japanese encephalitis virus[J]. Parasit Vectors, 2024, 17(1): 220. doi: 10.1186/s13071-024-06269-7

[2]

Franklinos LHV, Jones KE, Redding DW, et al. The effect of global change on mosquito-borne disease[J]. Lancet Infect Dis, 2019, 19(9): e302-e312. doi: 10.1016/S1473-3099(19)30161-6

[3]

Benelli G, Jeffries CL, Walker T. Biological control of mosquito vectors: past, present, and future[J]. Insects, 2016, 7(4): 52. doi: 10.3390/insects7040052

[4]

Liu N. Insecticide resistance in mosquitoes: Impact, mechanisms, and research directions[J]. Annu Rev Entomol, 2015, 60: 537. doi: 10.1146/annurev-ento-010814-020828

[5]

Almeida APG, Billingsley PF. Induced immunity against the mosquito Anopheles stephensi Liston (Diptera: Culicidae): Effects on mosquito survival and fecundity[J]. Int J Parasitol, 1998, 28(11): 1721-1731. doi: 10.1016/S0020-7519(98)00149-0

[6]

Almeida APG, Billingsley PF. Induced immunity against the mosquito Anopheles stephensi (Diptera: Culicidae): Effects of cell fraction antigens on survival, fecundity, and Plasmodium berghei (Eucoccidiida: Plasmodiidae) transmission[J]. J Med Entomol, 2002, 39(1): 207-214. doi: 10.1603/0022-2585-39.1.207

[7]

Lule-Chávez AN, Avila EE, González-de-la-Vara LE, et al. Detrimental effects of induced antibodies on Aedes aegypti reproduction[J]. Neotrop Entomol, 2019, 48(4): 706-716. doi: 10.1007/s13744-019-00678-5

[8]

Hatfield PR. Anti-mosquito antibodies and their effects on feeding, fecundity and mortality of Aedes aegypti[J]. Med Vet Entomol, 1988, 2(4): 331-338. doi: 10.1111/j.1365-2915.1988.tb00205.x

[9]

Ramasamy MS, Ramasamy R, Kay BH, et al. Anti-mosquito antibodies decrease the reproductive capacity of Aedes aegypti[J]. Med Vet Entomol, 1988, 2(1): 87-93. doi: 10.1111/j.1365-2915.1988.tb00053.x

[10]

Gakhar SK, Jhamb A, Gulia M, et al. Anti-mosquito ovary antibodies reduce the fecundity of Anopheles stephensi (Diptera: Insecta)[J]. Jpn J Infect Dis, 2001, 54(5): 181-183. doi: 10.7883/yoken.JJID.2001.181

[11]

Kemp DH, Agbede RIS, Johnston LAY, et al. Immunization of cattle against Boophilus microplus using extracts derived from adult female ticks: Feeding and survival of the parasite on vaccinated cattle[J]. Int J Parasitol, 1986, 16(2): 115-120. doi: 10.1016/0020-7519(86)90096-2

[12]

Lal AA, Patterson PS, Sacci JB, et al. Anti-mosquito midgut antibodies block development of Plasmodium falciparum and Plasmodium vivax in multiple species of Anopheles mosquitoes and reduce vector fecundity and survivorship[J]. Proc Natl Acad Sci U S A, 2001, 98(9): 5228-5233. doi: 10.1073/pnas.091447398

[13]

Song X, Wang M, Dong L, et al. PGRP-LD mediates A. stephensi vector competency by regulating homeostasis of microbiota-induced peritrophic matrix synthesis[J]. PLoS Pathog, 2018, 14(2): e1006899. doi: 10.1371/journal.ppat.1006899

[14]

Calle-Tobón A, Holguin-Rocha AF, Moore C, et al. Blood meals with active and heat-inactivated serum modifies the gene expression and microbiome of Aedes albopictus[J]. Front Microbiol, 2021, 12: 724345. doi: 10.3389/fmicb.2021.724345

[15]

Ratnayake OC, Chotiwan N, Saavedra-Rodriguez K, et al. The buzz in the field: The interaction between viruses, mosquitoes, and metabolism[J]. Front Cell Infect Microbiol, 2023, 13: 1128577. doi: 10.3389/fcimb.2023.1128577

[16]

Fuchs S, Behrends V, Bundy JG, et al. Phenylalanine metabolism regulates reproduction and parasite melanization in the malaria mosquito[J]. PLoS One, 2014, 9(1): e84865. doi: 10.1371/journal.pone.0084865

[17]

Rani J, De TD, Chauhan C, et al. Functional disruption of transferrin expression alters reproductive physiology in Anopheles culicifacies[J]. PLoS One, 2022, 17(3): e0264523. doi: 10.1371/journal.pone.0264523

[18]

Salinas ND, Ma R, McAleese H, et al. A self-assembling Pfs230D1-ferritin nanoparticle vaccine has potent and durable malaria transmission-reducing activity[J]. Vaccines, 2024, 12(5): 546. doi: 10.3390/vaccines12050546

[19]

Cui L, Kim K. Recent malaria outbreak in the USA: Risk of and response to malaria reintroduction in non-endemic regions[J]. Decod Infect Transm, 2024, 2: 100018. doi: 10.1016/j.dcit.2024.100018

[20]

Zhang S, Yang G, Yang J, et al. Global, regional, and national burden of malaria, 1990-2021: Findings from the global burden of disease study 2021[J]. Decod Infect Transm, 2024, 2: 100021. https://www.sciencedirect.com/unsupported_browser

[21]

Carrillo-Bustamante P, Costa G, Lampe L, et al. Evolutionary modelling indicates that mosquito metabolism shapes the life-history strategies of Plasmodium parasites[J]. Nat Commun, 2023, 14(1): 8139. doi: 10.1038/s41467-023-43810-1

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