Frontiers in veterinary science · 2026
Compartment-specific immune responses to BoAHV-1 transplacental infection in late gestation.
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Cheuquepán Felipe, Agulló-Ros Irene, Risalde María A, Burucúa Mercedes M, Quintana Silvina, Plá Natalia, Pérez Sandra E, Scioli María Valeria, Cantón Germán J, Moore Dadin P, Odeón Anselmo C, Marin Maia S, Morrell Eleonora L
Аннотация
Varicellovirus bovinealpha1 (BoAHV-1) is an important cause of reproductive failure in cattle and can induce abortion following transplacental infection during late gestation. However, immune-associated responses at the conceptus (placenta and fetus) remain incompletely understood. This study aimed to characterize maternal and fetal immune-associated responses to BoAHV-1 vertical infection by evaluating the expression of endosomal Toll-like receptors (TLR3, TLR7 and TLR9), cytokines, and the antimicrobial peptide BMAP28, together with the distribution of immune-cell markers in placental and fetal tissues. Pregnant dams (infected, n = 7; controls, n = 4) were experimentally infected with BoAHV-1 during late gestation and euthanized at 15 days post-infection (dpi). Peripheral blood leukocytes (PBLs) were collected at 3 and 10 dpi, and placental and fetal tissue samples were collected during necropsy. Relative mRNA expression of innate immune genes was assessed by RT-qPCR, while immune-cell markers were characterized by immunohistochemistry. Maternal tissues, including PBLs and placental caruncles, showed reduced expression of TLR9 and TNF-α. Fetal lungs showed increased expression of endosomal TLRs, TNF-α, IL-12 and BMAP28, accompanied by increase of CD3+ cells and iNOS-associated cells. The fetal spleen showed specific changes in gene expression, whereas the fetal liver presented a distinct transcriptional pattern with increased TLR expression and reduced cytokine transcript levels. Overall, BoAHV-1 transplacental late infection was associated with distinct patterns of immune-related gene expression and immune-cell marker distribution across maternal, placental and fetal tissues, providing an integrated view of immune-associated responses at day 15 post-infection.