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High-resolution proteomics unveils salivary gland disruption and saliva-hemolymph protein exchange in Plasmodium-infected mosquitoes

Author

Listed:
  • Thiago Luiz Alves e Silva

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Sachi Kanatani

    (Johns Hopkins University, The W. Harry Feinstone Department of Molecular Microbiology and Immunology and Johns Hopkins Malaria Research Institute, Bloomberg School of Public Health)

  • Ana Beatriz Barletta Ferreira

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Cindi L. Schwartz

    (National Institutes of Health, Microscopy Unit, Research Technologies Branch, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases)

  • Benjamin Liffner

    (Indiana University School of Medicine, Department of Pharmacology & Toxicology
    University of Adelaide, School of Biological Sciences
    University of Adelaide, Institute for Photonics and Advanced Sensing)

  • Octavio A. C. Talyuli

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Janet Olivas

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases
    New York University Grossman School of Medicine, Department of Pathology)

  • Bianca M. Nagata

    (National Institutes of Health, Infectious Disease Pathogenesis Section, National Institute of Allergy and Infectious Diseases)

  • Zarna Rajeshkumar Pala

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases
    University of Maryland, Biological Sciences Graduate Program)

  • Tales Pascini

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Derron A. Alves

    (National Institutes of Health, Infectious Disease Pathogenesis Section, National Institute of Allergy and Infectious Diseases)

  • Ming Zhao

    (National Institutes of Health, Research Technologies Branch, National Institute of Allergy and Infectious Diseases)

  • Motoshi Suzuki

    (National Institutes of Health, Research Technologies Branch, National Institute of Allergy and Infectious Diseases)

  • Lilian P. Dorner

    (University of Heidelberg Medical School, Integrative Parasitology, Center for Infectious Diseases)

  • Friedrich Frischknecht

    (University of Heidelberg Medical School, Integrative Parasitology, Center for Infectious Diseases
    DZIF Partner Site Heidelberg, German Center for Infection Research)

  • Isabelle Coppens

    (Johns Hopkins University, The W. Harry Feinstone Department of Molecular Microbiology and Immunology and Johns Hopkins Malaria Research Institute, Bloomberg School of Public Health)

  • Carolina Barillas-Mury

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Sabrina Absalon

    (Indiana University School of Medicine, Department of Pharmacology & Toxicology)

  • Jose M. C. Ribeiro

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

  • Photini Sinnis

    (Johns Hopkins University, The W. Harry Feinstone Department of Molecular Microbiology and Immunology and Johns Hopkins Malaria Research Institute, Bloomberg School of Public Health)

  • Joel Vega-Rodriguez

    (National Institutes of Health, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases)

Abstract

Plasmodium sporozoites, the infective stage of malaria, must invade the mosquito salivary glands (SGs) before being transmitted to a vertebrate host. However, the physiological and biochemical effects of this invasion remain largely unexplored. We examined the impact of Plasmodium infection on Anopheles gambiae salivary glands using high-resolution proteomics, gene expression, and morphological analysis. The data reveal differential expression of various proteins, including the enrichment of hemolymph-derived humoral proteins in infected salivary glands. These proteins diffuse into the SGs due to structural damage caused by the sporozoites during invasion, while saliva proteins diffuse out into the circulation. Moreover, proteomic analysis of saliva from P. berghei– or P. falciparum–infected mosquitoes revealed changes in composition, with a pronounced reduction of immune proteins relative to uninfected mosquitoes. This reduction is likely due to the association of these proteins with the surface of sporozoites and/or changes in the saliva’s physical properties within the invaded salivary secretory cavities. The saliva protein profiles from mosquitoes infected with both Plasmodium species are remarkably similar, suggesting a conserved interaction between sporozoites and salivary glands. Our results provide a foundation for understanding the molecular interactions between Plasmodium sporozoites and mosquito salivary glands.

Suggested Citation

  • Thiago Luiz Alves e Silva & Sachi Kanatani & Ana Beatriz Barletta Ferreira & Cindi L. Schwartz & Benjamin Liffner & Octavio A. C. Talyuli & Janet Olivas & Bianca M. Nagata & Zarna Rajeshkumar Pala & T, 2025. "High-resolution proteomics unveils salivary gland disruption and saliva-hemolymph protein exchange in Plasmodium-infected mosquitoes," Nature Communications, Nature, vol. 16(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-64837-6
    DOI: 10.1038/s41467-025-64837-6
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    as
    1. Zarna Rajeshkumar Pala & Thiago Luiz Alves e Silva & Mahnaz Minai & Benjamin Crews & Eduardo Patino-Martinez & Carmelo Carmona-Rivera & Paola Carolina Valenzuela Leon & Ines Martin-Martin & Yevel Flor, 2024. "Mosquito salivary apyrase regulates blood meal hemostasis and facilitates malaria parasite transmission," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    2. Xiaowei Sun & Jie Shen & Norbert Perrimon & Xue Kong & Dan Wang, 2023. "The endoribonuclease Arlr is required to maintain lipid homeostasis by downregulating lipolytic genes during aging," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    3. Sachie Kanatani & Deborah Stiffler & Teun Bousema & Gayane Yenokyan & Photini Sinnis, 2024. "Revisiting the Plasmodium sporozoite inoculum and elucidating the efficiency with which malaria parasites progress through the mosquito," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    4. Björn Schwanhäusser & Dorothea Busse & Na Li & Gunnar Dittmar & Johannes Schuchhardt & Jana Wolf & Wei Chen & Matthias Selbach, 2013. "Correction: Corrigendum: Global quantification of mammalian gene expression control," Nature, Nature, vol. 495(7439), pages 126-127, March.
    5. Tyler R. Schleicher & Jing Yang & Marianna Freudzon & Alison Rembisz & Samuel Craft & Madeleine Hamilton & Morven Graham & Godfree Mlambo & Abhai K. Tripathi & Yue Li & Peter Cresswell & Photini Sinni, 2018. "A mosquito salivary gland protein partially inhibits Plasmodium sporozoite cell traversal and transmission," Nature Communications, Nature, vol. 9(1), pages 1-12, December.
    6. G. Costa & M. Gildenhard & M. Eldering & R. L. Lindquist & A. E. Hauser & R. Sauerwein & C. Goosmann & V. Brinkmann & P. Carrillo-Bustamante & E. A. Levashina, 2018. "Non-competitive resource exploitation within mosquito shapes within-host malaria infectivity and virulence," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
    7. Scott E. Lindner & Kristian E. Swearingen & Melanie J. Shears & Michael P. Walker & Erin N. Vrana & Kevin J. Hart & Allen M. Minns & Photini Sinnis & Robert L. Moritz & Stefan H. I. Kappe, 2019. "Transcriptomics and proteomics reveal two waves of translational repression during the maturation of malaria parasite sporozoites," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
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