in

Behavioral heterogeneity in host seeking and post-feeding suppression among disease vector mosquitoes


Abstract

Female mosquitoes bite vertebrate hosts and consume their blood to obtain nutrients for egg production, with species-specific host preferences and host-seeking strategies. Biting-related behaviors are modulated by internal physiological states, such as the suppression of host-seeking after a full blood meal, a phenomenon that varies in timing and duration across mosquito species. Here, we establish a behavior monitoring and classification pipeline to systematically compare baseline host-seeking behavior and post-blood meal suppression in Aedes, Anopheles, and Culex mosquitoes. We find distinct behavioral signatures and notable interspecific differences in the onset and duration of host-seeking suppression. While Aedes and Anopheles host-seeking behaviors have been extensively studied in laboratory settings, comparable behavioral data for Culex have been limited. Our findings establish a framework to study host seeking across key vector species, providing comparative insight into the internal control of behavioral plasticity and offering a foundation for improved modeling of host interactions and vector control.

Similar content being viewed by others

Host feeding preferences of malaria vectors in an area of low malaria transmission

Monitoring biodiversity and detection of diverse vertebrate species with mosquito blood meal analysis at the DeLuca Preserve, Florida, USA

Sensory regulation of meal sorting in Aedes aegypti mosquitoes

Data availability

All raw data are provided in the associated data file, and all videos can be accessed at Zenodo (https://doi.org/10.5281/zenodo.15478199)70.

Code availability

All code is deposited in GitHub (https://github.com/Duvall-Lab/UeharaDongDuvall2025).

References

  1. The U.S. Department of Health and Human Services and the U.S. Centers for Disease Control And Prevention. The National Public Health Strategy to Prevent and Control Vector-Borne Diseases in People. U.S. DHHS, CDC (2024).

  2. Bowen, M. F. The sensory physiology of host-seeking behavior in mosquitoes. Annu. Rev. Entomol. 36, 139–158 (1991).

    Google Scholar 

  3. Raji, J. I. et al. Aedes aegypti mosquitoes detect acidic volatiles found in human odor using the IR8a pathway. Curr. Biol. 29, 1253–1262.e7 (2019).

    Google Scholar 

  4. Takken, W. & Verhulst, N. O. Host Preferences of Blood-Feeding Mosquitoes. Annu. Rev. Entomol. 58, 433–453 (2013).

    Google Scholar 

  5. Taylor, B. & Jones, M. D. The circadian rhythm of flight activity in the mosquito Aedes aegypti (L.). The phase-setting effects of light-on and light-off. J. Exp. Biol. 51, 59–70 (1969).

    Google Scholar 

  6. Rund, S. S. C., O’Donnell, A. J., Gentile, J. E. & Reece, S. E. Daily rhythms in mosquitoes and their consequences for malaria transmission. Insects 7, 1–20 (2016).

    Google Scholar 

  7. Liu, S. et al. Clock genes regulate mating activity rhythms in the vector mosquitoes, Aedes albopictus and Culex quinquefasciatus. PLoS Negl. Trop. Dis. 16, 1–21 (2022).

    Google Scholar 

  8. Godsey, M. S., Burkhalter, K., Delorey, M. & Savage, H. M. Seasonality and time of host-seeking activity of Culex tarsalis and floodwater Aedes in northern Colorado, 2006-2007. J. Am. Mosq. Control Assoc. 26, 148–159 (2010).

    Google Scholar 

  9. Paramasivan, R., Philip Samuel, P. & Selvaraj Pandian, R. Biting rhythm of vector mosquitoes in a rural ecosystem of South India. Int. J. Mosq. Res. 2, 106–113 (2015).

    Google Scholar 

  10. Hamer, G. L. et al. Culex pipiens (Diptera: Culicidae): a bridge vector of West Nile virus to humans. J. Med. Entomol. 45, 125–128 (2008).

    Google Scholar 

  11. McBride, C. S. et al. Evolution of mosquito preference for humans linked to an odorant receptor. Nature 515, 222–227 (2014).

    Google Scholar 

  12. Lindh, E. et al. The Italian 2017 outbreak chikungunya virus belongs to an emerging Aedes aegypti-adapted virus cluster introduced from the Indian subcontinent. Open Forum Infect. Dis. 6, 1–8 (2019).

  13. Davis, E. E. Development of lactic acid-receptor sensitivity and host-seeking behaviour in newly emerged female Aedes aegypti mosquitoes. J. Insect Physiol. 30, 211–215 (1984).

    Google Scholar 

  14. Judson, C. L. Feeding and oviposition behavior in the mosquito Aedes aegypti (L.).I. Preliminary studies of physiological control mechanisms. Biol. Bull. 133, 369–377 (1967).

    Google Scholar 

  15. Davis, E. E. Regulation of sensitivity in the peripheral chemoreceptor systems for host-seeking behavior by a haemolymph-borne factor in Aedes aegypti. J. Insect Physiol. 30, 179–183 (1984).

    Google Scholar 

  16. Briegel, H. & Hörler, E. Multiple Blood Meals as a Reproductive Strategy in Anopheles (Diptera: Culicidae). J. Med. Entomol. 30, 975–985 (1993).

    Google Scholar 

  17. Klowden, M. J. B. H., Klowden, M. J. & Briegel, H. Mosquito gonotrophic cycle and multiple feeding potential: Contrasts between Anopheles and Aedes (Diptera: Culicidae). J. Med. Entomol. 31, 618–622 (1994).

    Google Scholar 

  18. Farjana, T. & Tuno, N. Multiple blood feeding and host-seeking behavior in Aedes aegypti and Aedes albopictus (Diptera: Culicidae). J. Med. Entomol. 50, 838–846 (2013).

    Google Scholar 

  19. Mitchell, C. J. & Millian, K. Y. Continued host seeking by partially Engorged Culex tarsalis (Diptera: Culicidae) collected in nature. J. Med. Entomol. 18, 249–250 (1981).

    Google Scholar 

  20. Gillies, M. T. The recognition of age-groups within populations of Anopheles gambiae by the pre-gravid rate and the sporozoite rate. Ann. Trop. Medn Parasitol. 48, 58–74 (1954).

    Google Scholar 

  21. Klowden, M. J., Blackmer, J. L. & Chambers, G. M. Effects of Larval Nutrition on the Host-Seeking Behavior of Adult Aedes Aegypti Mosquitoes. J. Am. Mosq. Control Assoc. 4, 73–75 (1988).

    Google Scholar 

  22. Vinauger, C. & Chandrasegaran, K. Context-specific variation in life history traits and behavior of Aedes aegypti mosquitoes. Front. Insect Sci. 4,1–13 (2024).

  23. Takken, W. et al. Inhibition of host-seeking response and olfactory responsiveness in Anopheles gambiae following blood feeding. J. Insect Physiol. 47, 303–310 (2001).

    Google Scholar 

  24. Gangoso, L. et al. Determinants of the current and future distribution of the West Nile virus mosquito vector Culex pipiens in Spain. Environ. Res. 188, 1–11 (2020).

    Google Scholar 

  25. Roth, D. et al. West Nile Virus range expansion into British Columbia. Emerg. Infect. Dis. 16, 1251–1258 (2010).

    Google Scholar 

  26. Lupenza, E., Gasarasi, D. B. & Minzi, O. M. Lymphatic filariasis, infection status in Culex quinquefasciatus and Anopheles species after six rounds of mass drug administration in Masasi District, Tanzania. Infect. Dis. Poverty 10, 1–11 (2021).

  27. Mitchell, C. J. Diapause termination, gonoactivity, and differentiation of host-seeking behavior from blood-feeding behavior in Hibernating Culex tarsalis (Diptera: Culicidae). J. Med. Entomol. 18, 386–394 (1981).

    Google Scholar 

  28. Galun, R. Feeding response in Aedes aegypti: Stimulation by Adenosine Triphosphate. Science (1979) 142, 1674–1675 (1963).

    Google Scholar 

  29. Klowden, M. J. & Lea, A. O. Abdominal distention terminates subsequent host-seeking behaviour of Aedes aegypti following a blood meal. J. Insect Physiol. 25, 583–585 (1979).

    Google Scholar 

  30. Klowden, M. J. & Lea, A. O. Blood meal size as a factor affecting continued host-seeking by Aedes Aegypti (L.). Am. J. Trop. Med. Hyg. 27, 827–831 (1978).

    Google Scholar 

  31. Klowden, M. J. Distension-mediated egg maturation in the mosquito, Aedes aegypti. J. Insect Physiol. 33, 83–87 (1987).

    Google Scholar 

  32. Chambers, G. & Klowden, M. Distention and sugar feeding induce autogenous egg development by the Asian Tiger Mosquito (Diptera: Culicidae). Entomol. Soc. Am. 33, 1–7 (1996).

    Google Scholar 

  33. Brown, M. R. et al. Endogenous regulation of mosquito host-seeking behavior by a neuropeptide. J. Insect Physiol. 40, 399–406 (1994).

    Google Scholar 

  34. Duvall, L. B., Ramos-Espiritu, L., Barsoum, K. E., Glickman, J. F. & Vosshall, L. B. Small-molecule agonists of Ae. aegypti Neuropeptide Y receptor block mosquito biting. Cell 176, 687–701.e5 (2019).

    Google Scholar 

  35. Dou, X., Chen, K., Brown, M. R. & Strand, M. R. Reciprocal interactions between neuropeptide F and RYamide regulate host attraction in the mosquito Aedes aegypti. Proc. Natl. Acad. Sci. USA. 121, 1–11 (2024).

    Google Scholar 

  36. Bansal, P., Pillai, R., Babu, P. D. & Sen, S. Q. Two neuropeptides that promote blood-feeding in Anopheles stephensi mosquitoes. bioRxiv https://doi.org/10.1101/2024.05.15.594342 (2024).

  37. Klowden, M. J. & Lea, A. O. Humoral inhibition of host-seeking in Aedes aegypti during oocyte maturation. J. Insect Physiol. 25, 231–235 (1979).

    Google Scholar 

  38. Beach, R. Mosquitoes: biting behavior inhibited by Ecdysone. Science (1979) 205, 829–831 (1979).

    Google Scholar 

  39. Dittmer, J., Alafndi, A. & Gabrieli, P. Fat body–specific vitellogenin expression regulates host-seeking behaviour in the mosquito Aedes albopictus. PLoS Biol. 17, 1–26 (2019).

    Google Scholar 

  40. Klowden, M. J. The endogenous regulation of mosquito reproductive behavior. Experientia 46, 660–670 (1990).

    Google Scholar 

  41. Liesch, J., Bellani, L. L. & Vosshall, L. B. Functional and genetic characterization of neuropeptide Y-like receptors in Aedes aegypti. PLoS Negl. Trop. Dis. 7, e2486 (2013).

    Google Scholar 

  42. Castillo, J. S., Bellantuono, A. J. & DeGennaro, M. Quantifying mosquito attraction using a Uniport Olfactometer. Cold Spring Harb. Protoc. 2023, 789–794 (2023).

    Google Scholar 

  43. Jones, M. D. R. The programming of circadian flight-activity in relation to mating and the gonotrophic cycle in the mosquito, Aedes aegypti. Physiol. Entomol. 6, 307–313 (1981).

    Google Scholar 

  44. Dong, L., Bradford, E. F., Barnett, J. M. & Duvall, L. B. Post-biting behavioral reprogramming underlies reproductive efficiency in Aedes aegypti mosquitoes. Cell Rep. 44, 1–15 (2025).

    Google Scholar 

  45. Luxem, K. et al. Open-source tools for behavioral video analysis: Setup, methods, and best practices. Elife 12, 1–20 (2023).

    Google Scholar 

  46. Sorrells, T. R., Pandey, A., Rosas-Villegas, A. & Vosshall, L. B. A persistent behavioral state enables sustained predation of humans by mosquitoes. Elife 11, 1–23 (2022).

    Google Scholar 

  47. Hol, F. J., Lambrechts, L. & Prakash, M. BiteOscope, an open platform to study mosquito biting behavior. Elife 9, 1–24 (2020).

    Google Scholar 

  48. Main, B. J. et al. Whole-genome assembly of Culex tarsalis. G3: Genes, Genomes. Genetics 11, 1–5 (2021).

    Google Scholar 

  49. Neafsey, D. E. et al. Highly evolvable malaria vectors: The genomes of 16 Anopheles mosquitoes. Science (1979) 347, 1–8 (2015).

    Google Scholar 

  50. Reidenbach, K. R. et al. Phylogenetic analysis and temporal diversification of mosquitoes (Diptera: Culicidae) based on nuclear genes and morphology. BMC Evol. Biol. 9, 1–14 (2009).

    Google Scholar 

  51. Soghigian, J. et al. Phylogenomics reveals the history of host use in mosquitoes. Nat. Commun. 14, 1–14 (2023).

  52. Mathis, A. et al. DeepLabCut: markerless pose estimation of user-defined body parts with deep learning. Nat. Neurosci. 21, 1281–1289 (2018).

    Google Scholar 

  53. Luxem, K. et al. Identifying behavioral structure from deep variational embeddings of animal motion. Commun. Biol. 5, 1–15 (2022).

    Google Scholar 

  54. Scott, T. W. & Takken, W. Feeding strategies of anthropophilic mosquitoes result in increased risk of pathogen transmission. Trends Parasitol. 28, 114–121 (2012).

    Google Scholar 

  55. Tuno, N., Kjaerandsen, J., Badu, K. & Kruppa, T. Blood-Feeding Behavior of Anopheles gambiae and Anopheles melas in Ghana, Western Africa. J. Med. Entomol. 47, 28–31 (2010).

    Google Scholar 

  56. Degennaro, M. et al. Orco mutant mosquitoes lose strong preference for humans and are not repelled by volatile DEET. Nature 498, 487–491 (2013).

    Google Scholar 

  57. Rizzoli, A. et al. Understanding West Nile virus ecology in Europe: Culex pipiens host feeding preference in a hotspot of virus emergence. Parasit. Vectors 8, 1–13 (2015).

    Google Scholar 

  58. De Obaldia, M. E. et al. Differential mosquito attraction to humans is associated with skin-derived carboxylic acid levels. Cell 185, 4099–4116.e13 (2022).

    Google Scholar 

  59. Syed Z. & Leal W. S. Acute olfactory response of Culex mosquitoes to a human- and bird-derived attractant. Proc. Natl. Acad. Sci. 106, 18803–18808 (2009).

  60. Kilpatrick, A. M., Kramer, L. D., Jones, M. J., Marra, P. P. & Daszak, P. West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior. PLoS Biol. 4, 606–610 (2006).

    Google Scholar 

  61. Klowden, M. J. Initiation and termination of host-seeking. J. Insect. Physiol. 27, 799–803 (1981).

  62. Briegel, H. Metabolic relationship between female body size, reserves, and fecundity of Aedes aegypti. J. Insect Physiol. 36, 165–172 (1990).

    Google Scholar 

  63. Venkataraman, K. et al. Two novel, tightly linked, and rapidly evolving genes underlie Aedes aegypti mosquito reproductive resilience during drought. Elife 12, 1–36 (2023).

    Google Scholar 

  64. Judson, C. Physiology of feeding and oviposition behavior in Aedes aegypti (L.) experimental dissociation of feeding and oogenesis. J. Med. Entomol. 5, 21–23 (1968).

    Google Scholar 

  65. Eastwood, G., Cunningham, A. A., Kramer, L. D. & Goodman, S. J. The vector ecology of introduced Culex quinquefasciatus populations, and implications for future risk of West Nile virus emergence in the Galápagos archipelago. Med. Vet. Entomol. 33, 44–55 (2019).

    Google Scholar 

  66. Dong, L., Hormigo, R., Barnett, J. M., Greppi, C. & Duvall, L. B. Time-of-day modulation in mosquito response persistence to carbon dioxide is controlled by Pigment-Dispersing Factor. Proc. Natl. Acad. Sci. 122, 1–11 (2025).

  67. Benedict, M. Q. et al. Pragmatic selection of larval mosquito diets for insectary rearing of Anopheles gambiae and Aedes aegypti. PLoS One 15, 1–15 (2020).

  68. Hellhammer, F. et al. Impact of different diets on the survival, pupation, and adult emergence of Culex pipiens biotype molestus larvae, and infectability with the insect-specific Culex Y virus. Front. Trop. Dis. 4, 1–13 (2023).

  69. Giraldo, D. et al. An expanded neurogenetic toolkit to decode olfaction in the African malaria mosquito Anopheles gambiae. Cell Rep. Methods 4, 1–12 (2024).

  70. Uehara, T., Dong, L. & Duvall, L. Video data of mosquito behavior for the study “Behavioral heterogeneity host-seeking suppression among disease vector mosquitoes”. https://doi.org/10.5281/zenodo.15478199 (2026).

  71. Letunic, I. & Bork, P. Interactive Tree of Life (iTOL) v6: Recent updates to the phylogenetic tree display and annotation tool. Nucleic Acids Res. 52, W78–W82 (2024).

    Google Scholar 

Download references

Acknowledgements

We thank Thomas Gabel for assistance with animal husbandry, and Lindy McBride and Conor McMeniman for providing Anopheles and Culex strains. We thank Richard Hormigo and the Advanced Instrumentation group at the Mortimer B. Zuckerman Mind Brain Behavior Institute for support with assay development. We thank members of the Duvall lab for comments and useful discussions on the manuscript. This work was supported by the following grants: NIGMS (R35 GM137888) (LBD), Beckman Young Investigator Award (LBD), Pew Scholar in Biomedical Sciences Award (LBD), Klingenstein-Simons Fellowship Award in Neuroscience (LBD), JSPS Fostering Joint International Research (#21KK0273) (TU).

Author information

Authors and Affiliations

Authors

Contributions

TU and LBD designed experiments. TU performed behavioral experiments and TU and LD performed blood feeding and meal quantification. TU and LD designed behavioral assays, wrote code for the behavioral analyses, and analyzed the data. TU, LD, and LBD prepared the figures and wrote the manuscript.

Corresponding author

Correspondence to
Laura B. Duvall.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Communications Biology thanks the anonymous reviewers for their contribution to the peer review of this work. Primary Handling Editors: Nicolas Desneux and Mengtan Xing. A peer review file is available.

Additional information

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

Supplementary information

Supplementary Information (download PDF )

Description of Additional Supplementary Files (download DOCX )

Supplementary Data (download XLSX )

Reporting Summary (download PDF )

Transparent Peer Review file (download PDF )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Cite this article

Uehara, T., Dong, L. & Duvall, L.B. Behavioral heterogeneity in host seeking and post-feeding suppression among disease vector mosquitoes.
Commun Biol (2026). https://doi.org/10.1038/s42003-026-09987-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1038/s42003-026-09987-z


Source: Ecology - nature.com

A finely annotated dataset for the automated acoustic identification of European Orthoptera and Cicadidae

Spatiotemporal evolution and driving mechanisms of multiple scales ecological security in Shanxi Province from the perspective of service, risk and health

Back to Top