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Females are thought to gain better-quality genes for their offspring by mating with particular males. Genes of the major histocompatibility complex (MHC) play a critical role in adaptive immunity, and several studies have examined female mate choice in relation to MHC variation. In common yellowthroats, females prefer males that have larger black facial masks, an ornament associated with MHC variation, immune function and condition. Here we also tested whether mating patterns are directly correlated with MHC diversity or similarity. Using pyrosequencing, we found that the presence of extra-pair young in the brood was not related to male MHC diversity or similarity between the female and her within-pair mate. Furthermore, extra-pair sires did not differ in overall diversity from males they cuckolded, or in their similarity to the female. MHC diversity is extremely high in this species, and it may limit the ability of females to assess MHC variation in males. Thus, mating may be based on ornaments, such as mask size, which are better indicators of overall male health and genetic quality.
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http://dx.doi.org/10.1098/rspb.2012.1885 | DOI Listing |
Biology (Basel)
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Sichuan Ganzi Ecological Environment Monitoring Center, Ganzi 626700, China.
The endangered Bengal slow loris () relies heavily on captive/rescue populations for conservation. This study investigated the critical link between Major Histocompatibility Complex (MHC) class II DRB1 exon 2 () genetic variation and gut microbiota in 46 captive individuals, aiming to improve ex situ management. Using standardized conditions across three enclosure types, we characterized polymorphism via targeted sequencing and analyzed fecal microbiota using 16S rRNA gene amplicon sequencing.
View Article and Find Full Text PDFAIDS Res Ther
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Medical and Scientific Research Centre, University of Ghana Medical Centre, Legon, Accra, Ghana.
Background: Human Immunodeficiency Virus and malaria are significant public health challenges in sub-Saharan Africa, contributing substantially to morbidity and mortality in the region. The trajectory of HIV and malaria mono- and coinfections may be different with presentations of drug-drug and disease-disease interactions. Current medications of artemether-lumefantrine and dolutegravir (DTG) -based anti-retroviral therapy which are the preferred drugs are metabolised by CYP2B6, CYP3A4/5 and UGTs which are polymorphic and may contribute to drug disposition and clinical outcomes.
View Article and Find Full Text PDFImmunohorizons
August 2025
Biosettia Inc., San Diego, CA, United States.
The interactions between endogenous retroviruses (ERVs) and major histocompatibility complex molecules may significantly influence autoimmune diseases due to their common roles in the evolution and development of the adaptive immune system. Notably, regions within the Gag antigens of a specific group of ERVs, similar to murine leukemia retroviruses, exhibit patterns of sequence conservation, variation, and mutation. One highly conserved peptide of Gag, p5-13 (VTTPLSLTL), binds with high affinity to a nonclassic major histocompatibility complex molecule, Qa-1, and is preferentially recognized by T cells enriched in the pancreas of nonobese diabetic (NOD) mice, which spontaneously develop autoimmune type 1 diabetes.
View Article and Find Full Text PDFSci Rep
August 2025
Department of Stomatology, Northwest University First Hospital, Xi'an, Shaanxi, China.
Periodontitis is a common inflammatory disease affecting the tissues surrounding and supporting the teeth, ultimately leading to tooth loss if left untreated. This study aimed to investigate the diagnostic potential of lipid metabolism-related genes (LMRGs) and characterize the immune microenvironment landscape in periodontitis. Differential expression analysis identified differentially expressed LMRGs (DELMRGs), followed by functional enrichment analyses to elucidate their biological functions.
View Article and Find Full Text PDFJ Neurol
August 2025
Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Via Pansini 5, 80131, Naples, Italy.
Background: Ocrelizumab (OCR) is a humanized anti-CD20 monoclonal antibody approved for multiple sclerosis (MS). While its efficacy has been attributed to early and sustained B cell depletion, emerging evidence suggests a broader immunomodulatory profile.
Objectives: To investigate temporal dynamics of OCR-induced immune modulation in MS by analyzing pathway enrichment score changes in transcriptomic data from peripheral blood mononuclear cells (PBMCs) at early (2 weeks) and late (6 months) timepoints following treatment initiation.