Evidence map›Paper›PMID 42591436›Full record

ArticleFrontiers in immunology2026

Differential protein abundance in colostrum-derived extracellular vesicles from bovine leukemia virus-infected cattle are implicated in immune regulation and inflammation.

Cecilia Valeria Pérez, Hugo Adrián Carignano, Yamila Celeste Marchetti, Diego Daniel González, Vanesa Ruiz, Karina Gabriela Trono, Claudia Mongini

Abstract read
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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Cecilia Valeria PérezLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Hugo Adrián CarignanoLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Yamila Celeste MarchettiLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Diego Daniel GonzálezLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Vanesa RuizLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Karina Gabriela TronoLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.
Claudia MonginiLaboratorio de Estudio de Vesículas Extracelulares y miRNA. Instituto de Virología e Innovaciones Tecnológicas (IVIT), Instituto Nacional de Tecnología Agropecuaria (INTA) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET). Hurlingham, Buenos Aires, Argentina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bovine leukemia virus (BLV) is an oncogenic retrovirus that naturally infects cattle. Once infected, the virus persists indefinitely throughout life at a transcriptionally silent stage. Soon after infection, humoral and cytotoxic activities efficiently abolish the viral replicative cycle, allowing only mitotic expansion of provirus-carrying cells. These anti-viral activities persist throughout the animal's life indicating that the immune system is permanently stimulated by BLV antigens. Although protein production is abolished during the chronic stage, viral transcription is not completely shut down. Extracellular vesicles (EVs) are nano-sized lipid bilayer vesicles released from most cells and play multiple roles in cell-to-cell communication, including immune modulation, angiogenesis, and transformation of cells by transferring genetic material and functional proteins. Colostrum is rich in EVs that carry bioactive proteins and RNAs reflecting maternal physiology and immune status. In this study, we aimed to characterize how BLV infection influences the protein cargo of colostrum-derived EVs. Methods: Colostral EVs were isolated using a protocol that combines acid pre-treatment with ultracentrifugation on sucrose gradients. Results: Transmission electron microscopy and nanoparticle tracking analysis revealed a heterogeneous population of vesicles ranging from 40 to 120 nm in diameter, exhibiting the characteristic morphology of EVs. Flow cytometry analysis confirmed the presence of the EV marker CD9. In addition, the presence of CD63, CD81, and TSG101 was also detected by Western blot. Quantitative proteomic analysis using a mass spectrometer coupled to liquid chromatography (LC/MS) revealed a total of 13 bovine differentially abundant proteins (FDR < 0.05 and FC ≥ |1.5|) from a total of 1,082 proteins identified. Among them, 9 (69.2%) showed decreased abundance (e,g., ANXA1, CLU, DMBT1, LRRC32), whereas 4 (30.8%) showed an increased abundance (e.g., IDO1, MARCKS, LCP1) in the group of BLV-infected animals. Enrichment analysis showed that differentially abundant proteins were primarily associated with immune-related processes, including complement activation and immunoglobulin-mediated immunity, as well as cellular metabolic processes, cytoskeletal organization, intracellular signaling and vesicle trafficking. Discussion: Overall, the results observed in colostrum-derived EVs from BLV-infected cows provide compelling evidence that BLV infection induced systemic molecular alterations that may modulate inflammation and the immune response in calves.

Indexed as

ColostrumEnzootic Bovine LeukosisExtracellular VesiclesInflammationLeukemia Virus, BovineAnimalsCattleFemaleProteomicsbovine leukemia viruscolostrumextracellular vesiclesimmune responseproteomics

Identifiers

PMID42591436
PMCPMC13461735

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