Ovulation-inducing factor: a protein component of llama seminal plasma

• Published in: Reproductive biology and endocrinology Vol. 8; no. 1; p. 44
• Main Authors: Ratto, Marcelo H, Huanca, Wilfredo, Adams, Gregg P
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 12.05.2010; BioMed Central; BMC
• Subjects: Animals; Camelids, New World - physiology; Cell Size - drug effects; Chemical Fractionation - methods; Data collection; Enzymes; Experiments; Female; Females; Llamas; Male; Molecular Weight; Ovarian Follicle - cytology; Ovarian Follicle - drug effects; Ovulation; Ovulation - drug effects; Ovulation - physiology; Ovulation Induction - methods; Physiological aspects; Plasma; Seminal Plasma Proteins - chemistry; Seminal Plasma Proteins - isolation & purification; Seminal Plasma Proteins - pharmacology; Seminal Plasma Proteins - physiology; Sperm; Studies; United States
• ISSN: 1477-7827; 1477-7827
• DOI: 10.1186/1477-7827-8-44

Previously, we documented the presence of ovulation-inducing factor (OIF) in the seminal plasma of llamas and alpacas. The purpose of the study was to define the biochemical characteristics of the molecule(s) in seminal plasma responsible for inducing ovulation. In Experiment 1, llama seminal plasma was centrifuged using filtration devices with nominal molecular mass cut-offs of 30, 10 and 5 kDa. Female llamas (n = 9 per group) were treated i.m. with whole seminal plasma (positive control), phosphate-buffered saline (negative control), or the fraction of seminal plasma equal or higher than 30 kDa, 10 to 30 kDa, 5 to 10 kDa, or < 5 kDa. In Experiment 2, female llamas (n = 7 per group) were given an i.m. dose of seminal plasma treated previously by: 1) enzymatic digestion with proteinase-K, 2) incubation with charcoal-dextran, 3) heating to 65 degrees C, or 4) untreated (control). In Experiment 3, female llamas (n = 10 per group) were given an i.m. dose of pronase-treated or non-treated (control) seminal plasma. In all experiments, llamas were examined by transrectal ultrasonography to detect ovulation and CL formation. Ovulation rate was compared among groups by Fisher's exact test and follicle and CL diameters were compared among groups by analyses of variance or student's t-tests. In Experiment 1, all llamas in the equal or higher than 30 kDa and positive control groups ovulated (9/9 in each), but none ovulated in the other groups (P < 0.001). In Experiment 2, ovulations were detected in all llamas in each treatment group; i.e., respective treatments of seminal plasma failed to inactivate the ovulation-inducing factor. In Experiment 3, ovulations were detected in 0/10 llamas given pronase-treated seminal plasma and in 9/10 controls (P < 0.01). We conclude that ovulation-inducing factor (OIF) in llama seminal plasma is a protein molecule that is resistant to heat and enzymatic digestion with proteinase K, and has a molecular mass of approximately equal or higher than 30 kDa.