Artificial insemination (AI) with liquid -preserved stallion semen is a widely used reproductive technology. As the demand for AI doses of high-class stallions is transnational, they are frequently exposed to long-distance transport. Since recent studies in boars indicated that vibration emissions caused by transport negatively affected sperm quality in vitro, this study questioned whether sperm quality in stallions is similarly impaired. Furthermore, we investigated stallion and extender -related differences in the spermatozoa's resistance to transport -related quality loss. Stallion ejaculates (n = 30) were collected at a German AI center, split in half, and subsequently diluted to a final sperm concentration of 50 x 10(6 )sperm/mL using the semen extenders EquiPlus or Gent (both Minitub GmbH, Germany). Four 12 mL aliquots of each sample were filled in plastic syringes according to a split -sample design and exposed to vibration (Displacement index D-i = 3.0 +/- 0.1) at 5 C-degrees for 0 h (control), 3 h, 6 h or 9 h. All samples were stored for four days at 5 C after transport simulation and analyzed for total sperm motility, thermo-resistance, membrane integrity, and mitochondrial activity determined by flow cytometry as well as the pH. After calculating generalized linear mixed models for each sperm quality trait, a negative impact of the duration of transport simulation could be shown on total sperm motility (P = 0.001), thermo-resistance (P = 0.030), and the pH (P = 0.001). Simulated transport for 6 h and 9 h diminished sperm quality (P <= 0.01), with 9 h reducing thermo-resistance by 5 +/- 2.2% points (PP) for EquiPlus and sperm motility by 2.2 +/- 1.7 PP for Gent compared to the control group. In contrast, samples exposed to vibration for 3 h showed no decline in sperm quality (P > 0.05). The individual stallion influenced every semen trait (P < 0.05) and transport -related losses in sperm thermo-resistance of up to 15.9 PP were demonstrated. Furthermore, EquiPlus was superior to Gent in all semen assessments (P < 0.001). We conclude that in vitro sperm quality is impaired by vibration. As the quality loss depends on the transport time, we recommend keeping shipping time as short as possible especially for spermatozoa of stallions that are susceptible to vibration -induced sperm quality loss.
