Aichi virus inactivation by heat in 2-ml glass vials

Aichi virus (AiV) that results in gastroenteritis worldwide, is spread through contaminated shellfish and water. The resistance/tolerance of AiV to common inactivation processes along with the absence of commercially available vaccines makes it necessary to study its thermal inactivation kinetics. This research evaluated the heat inactivation of AiV in cell-culture media using 2-ml sterile glass vials by the linear and Weibull models. Heat treatments of AiV titers of 7 log plaque forming units (PFU)/ml were conducted thrice in a water-bath at 50, 54, and 58 degrees C for up to 90 min. Plaque assays for each dilution in duplicate were used to determine infectious virus titers. Linear model D-values for AiV at 50 +/- 1 degrees C (+/- = standard error) (come-up time = 68 s), 54 +/- 0.7 degrees C (130 s), and 58 +/- 0.6 degrees C (251 s) were 43.3 +/- 4.23 (R-2 = 0.40, RMSE = 0.56), 5.69 +/- 0.28 (R-2 = 0.80, RMSE = 0.43), and 1.20 +/- 0.63 min (R-2 = 0.69, RMSE = 0.39), respectively, and the linear model z-value was 5.14 +/- 0.39 degrees C (R-2 = 0.99, RMSE = 0.08). For the same temperatures, the Weibull model t(d = 1) values were 20.98 +/- 8.8 (R-2 = 0.62, RMSE = 0.46, alpha (scale parameter) = 2.30, beta (shape parameter) = 0.38), 3.84 +/- 0.69 (R-2 = 0.85, RMSE = 0.38, alpha = 1.08, beta = 0.66), and 0.87 +/- 0.10 min (R-2 = 0.80, RMSE = 0.32, alpha = 0.22, beta = 0.61), respectively and the z-value (using T-d = 1) was 5.79 +/- 0.22 degrees C (R-2 = 1.0, RMSE = 0.03). A better fit was obtained with the Weibull model for log reductions versus time with higher R-2 and lower RMSE values. Application of AiV inactivation parameters can help reduce the risk of AiV outbreaks.