Expression profiling of human milk derived exosomal microRNAs and their targets in HIV-1 infected mothers

• Published in: Scientific reports 2020-07, Vol.10 (1), p.12931-12931, Article 12931
• Main Authors: Zahoor, Muhammad Atif, Yao, Xiao-Dan, Henrick, Bethany M., Verschoor, Chris P., Abimiku, Alash’le, Osawe, Sophia, Rosenthal, Kenneth L.
• Format: Article
• Language: English
• Subjects: 631/250/255; 631/250/255/1901; Adult; Antiretroviral agents; Antiretroviral therapy; Apoptosis; Biosynthesis; Breast milk; Cell cycle; Circulating MicroRNA - biosynthesis; Circulating MicroRNA - genetics; Disease transmission; Exosomes; Exosomes - genetics; Exosomes - metabolism; Female; Forkhead protein; Gene Expression Profiling; Gene Expression Regulation; HIV; HIV Infections - genetics; HIV Infections - metabolism; HIV-1 - metabolism; Human immunodeficiency virus; Humanities and Social Sciences; Humans; Infants; MicroRNAs; Milk, Human - metabolism; miRNA; Mothers; multidisciplinary; Neonates; p53 Protein; Postpartum; Science; Science (multidisciplinary); Signal transduction
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-69799-x

Despite the use of antiretroviral therapy (ART) in HIV-1 infected mothers approximately 5% of new HIV-1 infections still occur in breastfed infants annually, which warrants for the development of novel strategies to prevent new HIV-1 infections in infants. Human milk (HM) exosomes are highly enriched in microRNAs (miRNAs), which play an important role in neonatal immunity. Furthermore, HM exosomes from healthy donors are known to inhibit HIV-1 infection and transmission; however, the effect of HIV-1 on HM exosomal miRNA signatures remains unknown. In this study, we used nCounter NanoString technology and investigated miRNAs expression profiles in first week postpartum HM exosomes from HIV-1 infected and uninfected control mothers (n = 36). Our results indicated that HIV-1 perturbed the differential expression patterns of 19 miRNAs (13 upregulated and 6 downregulated) in HIV-1 infected women compared to healthy controls. DIANA-miR functional pathway analyses revealed that multiple biological pathways are involved including cell cycle, pathways in cancer, TGF-β signaling, FoxO signaling, fatty acid biosynthesis, p53 signaling and apoptosis. Moreover, the receiver operating characteristics (ROC) curve analyses of miR-630 and miR-378g yielded areas under the ROC curves of 0.82 (95% CI 0.67 to 0.82) and 0.83 (95% CI 0.67 to 0.83), respectively highlighting their potential to serve as biomarkers to identify HIV-1 infection in women. These data may contribute to the development of new therapeutic strategies in prevention of mother-to-child transmission (MTCT) of HIV-1.