Evidence map›Paper›PMID 40113878›Full record

ArticleScientific reports2025

Biochemical and physiological characterization of Aedes aegypti midgut chymotrypsin.

Abigail G Ramirez, Jun Isoe, Mateus Sá Magalhães Serafim, Daniel Fong, My Anh Le, James T Nguyen, Olive E Burata, Rachael M Lucero, Rebecca K Spangler, Alberto A Rascón

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Abigail G Ramirez *School of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA.
Jun Isoe *School of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA.
Mateus Sá Magalhães SerafimDepartment of Microbiology, Federal University of Minas Gerais, Belo Horizonte, 31270-901, Minas Gerais, Brazil.
Daniel FongSchool of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA.
My Anh LeSchool of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA.
James T NguyenSchool of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA.
Olive E BurataDepartment of Chemistry, San José State University, 1 Washington Square, San José, CA, 95112, USA.
Rachael M LuceroDepartment of Chemistry, San José State University, 1 Washington Square, San José, CA, 95112, USA.
Rebecca K SpanglerDepartment of Chemistry, San José State University, 1 Washington Square, San José, CA, 95112, USA.
Alberto A RascónSchool of Molecular Sciences, Arizona State University, 551 E. University Dr., Tempe, AZ, 85281, USA. aarasco1@asu.edu.

Funding

Vector Control Strategy Through Inhibition of Aedes aegypti Midgut ProteasesSC3GM116681 · NIGMS · SAN JOSE STATE UNIVERSITY · PI RASCON, ALBERTO A · 2016 to 2023
$847k
NIGMS NIH HHS SC3 GM116681NIGMS NIH HHS SC3GM116681
6 · The paper itself

Abstract

The Aedes aegypti mosquito is a vector of dengue, Zika, and chikungunya. The mosquito's reliance on blood facilitates the transmission of these viral pathogens to humans. Digestion of blood proteins depends on the biphasic expression of serine proteases, with trypsin-like activity contributing to most of the activity in the midgut. Other proteases found (serine collagenase- and chymotrypsin-like) are thought to contribute to digestion, but their roles are largely understudied. Thus, elucidating the activity and specific roles of all midgut proteases will help understand the complexity of the digestion process and help validate them as potential targets for the development of a new vector control strategy. Herein, we focused on characterizing the activity profile and role of Ae. aegypti chymotrypsin (AaCHYMO). Knockdown studies resulted in elimination and significant reduction of chymotrypsin-like activity in blood fed midgut extracts, while in vitro fluorescent and blood protein digestion assays revealed important substrate specificity differences. Interestingly, knockdown of AaCHYMO did not impact fecundity, indicating the presence of an intricate network of proteases working collectively to degrade blood proteins. Further, knockdown of the ecdysone receptor (EcR) led to a decrease in overall AaCHYMO expression and activity in the mosquito, which may play an important regulatory role.

Indexed as

AedesChymotrypsinGastrointestinal TractInsect ProteinsAnimalsFemaleGene Knockdown TechniquesMosquito VectorsSubstrate SpecificityChymotrypsinInsect ProteinsAedes aegyptiBlood meal digestionChymotrypsinEnzyme kineticsRNA interference (RNAi)Vector control

Identifiers

PMID40113878
PMCPMC11926125

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.