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Mosquito saliva contains numerous distinct mosquito salivary proteins (MSPs) that mediate mosquito-host interactions. Repeated mosquito exposure can trigger allergic reactions, with MSP-specific IgE playing a central role. Current enzyme-linked immunosorbent assay (ELISA) and immunoblotting methods for detecting MSP-specific IgE suffer from interference by much more abundant MSP-specific IgG, leading to low sensitivity. Here, we developed a capture ELISA to overcome these limitations. We compared the performance of this capture ELISA with the conventional indirect ELISA in detecting MSP-specific IgE titers in sera from both repeatedly exposed mice and human volunteers. The results demonstrated that, compared to the indirect ELISA, the novel capture ELISA exhibited significantly superior sensitivity and specificity. Using serum samples from 20 volunteers with confirmed exposure to Aedes aegypti bites and 20 volunteers without such exposure, we found that the capture ELISA achieved 100% diagnostic sensitivity and specificity (20/20), with both false-positive and false-negative rates at 0% (0/20). The limit of detection was determined to be 87.42 ng/mL total IgE equivalent in human serum. Furthermore, we dynamically monitored Aedes aegypti salivary protein AAEL000749-specific IgE titers in healthy individuals from areas with widespread mosquito distribution using the capture ELISA. The results showed that both the positive rate and titer of AAEL000749-specific IgE in the sera were significantly higher during months with elevated mosquito population densities, compared to months with lower densities. This indicates that, under natural exposure conditions, the levels of MSP-specific IgE in human sera are closely correlated with local mosquito densities. In summary, our novel capture ELISA demonstrates excellent diagnostic performance and can be used for the quantitative analysis of MSP-specific IgE in mammalian sera. This provides a powerful tool for the diagnosis and prognosis of mosquito allergy, as well as for monitoring mosquito exposure levels in endemic areas.
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http://dx.doi.org/10.1371/journal.pntd.0013468 | DOI Listing |
ACS Sens
September 2025
Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan 48109, United States.
We present a bioassay platform that leverages the lasing threshold distribution in a microlaser ensemble (ME), consisting of hundreds of individual microlasers, to measure analyte concentrations in solution. An ME is formed by placing dye-doped microbeads in a micro Fabry-Perot cavity. The microbeads are surface-modified with biorecognition molecules to capture analytes, while the quenchers resulting from the presence of the analytes on the microbeads' surfaces increase the lasing thresholds of the microlasers.
View Article and Find Full Text PDFACS Synth Biol
September 2025
Department of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, United States.
Rapid and portable antigen detection is essential for managing infectious diseases and responding to toxic exposures, yet current methods face significant limitations. Highly sensitive platforms like the Enzyme-Linked Immunosorbent Assay (ELISA) are time- and cost-prohibitive for point-of-need detection, while portable options like lateral flow assays (LFAs) require systemic overhauls for new targets. Furthermore, the complex infrastructure, high production costs, and extended timelines for assay development constrain the manufacturing of traditional diagnostic platforms in low-resource settings.
View Article and Find Full Text PDFCirc Res
September 2025
Department of Pediatrics, Child Health Research Center, University of Virginia School of Medicine, Charlottesville. (H.Y., M.Y., D.M., F.X., J.P.S., S.C., L.F.A., S.M., R.A.G., M.L.S.S.-L.).
Background: Juxtaglomerular cells are sensors that control blood pressure and fluid-electrolyte homeostasis. They are arranged as clusters at the tip of each afferent arteriole. In response to decreased blood pressure or extracellular fluid volume, juxtaglomerular cells secrete renin, initiating an enzymatic cascade that culminates in the production of Ang II (angiotensin II), a potent vasoconstrictor that restores blood pressure and fluid-electrolyte homeostasis.
View Article and Find Full Text PDFInt J Gen Med
August 2025
Department of Rheumatology and Clinical Immunology, Ningbo Medical Center Lihuili Hospital, The Affiliated Li Huili Hospital, Ningbo University, Ningbo, People's Republic of China.
Background: In this study, we investigated the role of neutrophil-derived exosomal miR-30d-5p in systemic lupus erythematosus (SLE).
Methods: We extracted exosomes from the neutrophils collected from SLE patients and healthy donors and analyzed the relative level of miR-30d-5p. The exosomes were characterized by transmission electron microscopy (TEM) and nanoparticle tracking analysis (NTA).
Analyst
September 2025
Department of Bioengineering, Izmir Institute of Technology, Izmir 35430, Türkiye.
Chronic kidney diseases (CKDs), which often end in kidney failure for many people around the world, have an important place in public health given that they also trigger other diseases. Therefore, the development of fast and cost-effective diagnostic technologies enables effective monitoring of patients and early diagnosis. Here, using the Enzyme-Linked Immunosorbent Assay (ELISA) principle, serum creatinine concentrations were determined using the developed lab-on-a-chip (LOC) platform.
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