Evidence map›Paper›PMID 42148768›Full record

ArticleVeterinary medicine and science2026

Sex Determination of X and Y Separated Fresh Bull Sperm Using SRY Gene Copy Number Analysis.

Ali Kadivar, Arash Rasouli, Naser Shams Esfandabadi, Najmeh Davoodian, Hassan Nazari, Seyed Abbas Mirzaei, Ebrahim Ahmadi, Hamid Rahimi

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Article in Veterinary medicine and science, 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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5 · Who and what money

Authors and funding

8 authors.

Ali KadivarDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.
Arash RasouliDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.
Naser Shams EsfandabadiDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran.
Najmeh DavoodianResearch Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.
Hassan NazariResearch Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.
Seyed Abbas MirzaeiCellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Ebrahim AhmadiResearch Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.
Hamid RahimiResearch Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran.

Funding

Shahrekord University 0GRD34M1576
6 · The paper itself

Abstract

BACKGROUND AND

objectiveThe present study employed absolute quantitative PCR to determine the sex of sperm fractions after subjecting fresh bull semen to motility-based separation using resiquimod, an agonist of Toll-like receptors 7 and 8, which is supposed to selectively impair the motility of sperm carrying the X chromosome.

methodsThe upper and lower fractions obtained from fresh bull sperm following the swim-up procedure, in both the control (untreated) and resiquimod-treated groups, were subjected to sperm DNA extraction and absolute quantification by real-time PCR to determine the number of Y chromosome-bearing sperm. Ten different dilutions were prepared from the cloned plasmid with SRY sequence. Isolated sperms from the upper and lower layers in the resiquimod-treated group and the fresh non-treated sperm were also used for in vitro embryo production.

resultsThe SRY gene copy number was significantly higher in the upper than the lower layer in the resiquimod-treated group (p < 0.05). The sex of the embryos produced with sperm harvested from the upper and lower layers of the treatment group confirmed the results of the PCR, because the number of male embryos produced from the upper layer sperm was significantly higher than the lower layer (73.33% vs. 28.57%) (p < 0.05).

conclusionConsidering that this sexing method is low-cost and can be done with little facilities, it can be used in the future for the isolation of X and Y sperms in bulls.

Indexed as

Gene DosageGenes, srySex Determination AnalysisSpermatozoaX ChromosomeY ChromosomeAnimalsCattleFemaleMaleReal-Time Polymerase Chain Reactionbull spermembryoreal‐time PCRresiquimodswim‐up

Identifiers

PMID42148768
PMCPMC13181913

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.