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Cited by 6Ion Transport and Channel RegulationVector-borne infectious diseasesStudy of Mite Species

The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.

Function and evolution of the aquaporin IsAQP1 in the Lyme disease vector Ixodes scapularis

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Published version of a preprint

Abstract

Ticks are important vectors of pathogenic viruses, bacteria, and protozoans to humans, wildlife, and domestic animals. Due to their life cycles, ticks face significant challenges related to water homeostasis. When blood‐feeding, they must excrete water and ions, but when off‐host (for stretches lasting several months), they must conserve water to avoid desiccation. Aquaporins (AQPs), a family of membrane‐bound water channels, are key players in osmoregulation in many animals but remain poorly characterized in ticks. Here, we bioinformatically identified AQP‐like genes from the deer tick Ixodes scapularis and used phylogenetic approaches to map the evolution of the aquaporin gene family in arthropods. Most arachnid AQP‐like sequences (including those of I. scapularis ) formed a monophyletic group clustered within aquaglycerolporins (GLPs) from bacteria to vertebrates. This gene family is absent from insects, revealing divergent evolutionary paths for AQPs in different hematophagous arthropods. Next, we sequenced the full‐length cDNA of I. scapularis aquaporin 1 ( IsAQP1 ) and expressed it heterologously in Xenopus oocytes to functionally characterize its permeability to water and solutes. Additionally, we examined IsAQP1 expression across different life stages and adult female organs. We found IsAQP1 is an efficient water channel with high expression in salivary glands prior to feeding, suggesting it plays a role in osmoregulation before or during blood feeding. Its functional properties are unique: unlike most GLPs, IsAQP1 has low glycerol permeability, and unlike most AQPs, it is insensitive to mercury. Together, our results suggest IsAQP1 plays an important role in tick water balance physiology and that it may hold promise as a target of novel vector control efforts.

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Research works printed but not linked: 1

  1. 10.1603/0022-2585(2008)45[68:aapfto]2.0.co;2 · DOI

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Metadata

Authors
Tsujimoto, H., Metz, H. C., Smith, A. A., Sakamoto, J. M., Pal, U., & Rasgon, J. L.
Affiliations
  • Pennsylvania State University (US)
  • University of Maryland, College Park (US)
Corresponding author
Rasgon, Jason L.
Venue
Insect Molecular Biology
Publisher
Wiley
Published
2023-02-22
Volume
32
Issue
4
Pages
329-339
ISSN
  • 0962-1075 (ISSN-L)
  • 1365-2583
OpenAlex
W4317679762
Cited by
6
References
71
Citations by year
2025: 3 · 2024: 1 · 2023: 2
FWCI
0.53
Type
journal article
Language
en
Open access
Locations
  • Insect Molecular Biology (publishedVersion, cc-by-nc-nd)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
Funders
  • U.S. Department of Agriculture (PEN04769)
  • Pennsylvania Department of Health
  • Directorate for Biological Sciences (1645331)
  • National Institute of Allergy and Infectious Diseases (R01AI080615)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
  • Life Sciences › Immunology and Microbiology › Parasitology › Vector-borne infectious diseases
  • Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Study of Mite Species
Keywords
aquaporins, Ixodes scapularis, osmoregulation, water homeostasis, glycerol permeability, salivary glands, tick life stages, vector control, hematophagous arthropods
MeSH terms
Animals, Bacteria, Disease Vectors, Female, Humans, Lyme Disease, Phylogeny, Water, Ixodes, Aquaporin 1

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CoChat. (2026). Citation check: Function and evolution of the aquaporin IsAQP1 in the Lyme disease vector Ixodes scapularis. https://app.cochat.ai/papers/10.1111/imb.12833
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Tsujimoto, H., Metz, H. C., Smith, A. A., Sakamoto, J. M., Pal, U., & Rasgon, J. L. (2023). Function and evolution of the aquaporin IsAQP1 in the Lyme disease vector Ixodes scapularis. Insect Molecular Biology. https://doi.org/10.1111/imb.12833

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.