Vassiliadis P, Kalapothaki V, Mavrommati C, Trichopoulos D
J Hyg (Lond). 1984 Aug;93(1):51-8. doi: 10.1017/s0022172400060927.
The Rappaport-Vassiliadis enrichment medium (RV medium) in 10 ml quantities (RV/43 degrees C, 10 ml) inoculated with 0.1 ml of pre-enrichment medium (P medium) was found more efficient in the isolation of salmonellae from 409 pre-enriched samples (mainly meat products), than the original Rappaport medium incubated at 43 degrees C (R/43 degrees C) and the RV medium in 5 ml quantities (RV/43 degrees C, 5 ml) inoculated with 0.01 ml of P medium (P less than 0.001, in both instances). Therefore, the inoculum from pre-enriched foods should not be less than 0.1 ml in 10 ml of RV medium. The RV/43 degrees, 10 ml was also better (P less than 0.01) in detecting samples containing salmonellas than the original Rappaport medium incubated at 37 degrees C (R/37 degrees C, 10 ml) and the modification R25 of R medium incubated at 37 degrees C. The R25 modification was used in 10 ml quantities (R25/37 degrees C, 10 ml) inoculated with 0.1 ml of P medium and in 5 ml quantities (R25/37 degrees, 5 ml) inoculated with 0.01 ml of P medium. The last two R25 procedures were of the same efficiency in isolating salmonellas from meat products.
研究发现,用10毫升拉帕波特 - 瓦西利亚迪斯增菌培养基(RV培养基)(RV/43℃,10毫升)接种0.1毫升预增菌培养基(P培养基),从409份预增菌样本(主要是肉类产品)中分离沙门氏菌,比在43℃培养的原始拉帕波特培养基(R/43℃)以及用5毫升RV培养基(RV/43℃,5毫升)接种0.01毫升P培养基的方法更有效(两种情况P均小于0.001)。因此,在10毫升RV培养基中,来自预增菌食品的接种量不应少于0.1毫升。在检测含有沙门氏菌的样本方面,10毫升的RV/43℃培养基也比在37℃培养的原始拉帕波特培养基(R/37℃,10毫升)以及在37℃培养的R培养基改良版R25更好(P小于0.01)。R25改良版用于10毫升的量(R25/37℃,10毫升)接种0.1毫升P培养基以及5毫升的量(R25/37℃,5毫升)接种0.01毫升P培养基。最后两种R25方法从肉类产品中分离沙门氏菌的效率相同。