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Viability and nematophagous activity of the freeze-dried fungus Arthrobotrys robusta against Ancylostoma spp. infective larvae in dogs

机译:冷冻干燥真菌强壮型节肢动物对Ansylostostoma spp的活力和食道活性。狗的感染性幼虫

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Viability and in vitro and in vivo activities of freeze-dried conidia of the predatory fungus Arthrobotrys robusta (1-31) were evaluated against infective larvae (L-3) of Ancylostoma spp. in dogs. A. robusta conidia were lyophilized and stored at 4 degrees C for a month. Freeze-dried conidia were diluted to 1 x 10(3) conidia/ml and tested in vivo. The treated group consisted of a solution containing conidia (1 ml) and 1000 Ancylostoma spp. (L-3) placed on Petri dishes plated with 2% water-agar (2% WA), at 25 degrees C, in the dark for 10 days. The control group consisted of 1000 Ancylostoma spp. L-3, plated on 2% WA. After 10 days, Ancylostoma spp. L-3 from both the treated and the control groups were recovered and counted. The in vivo test was performed on two dogs by administering a single oral dose of freeze-dried conidia (1.5 x 10(5)) in aqueous solution to one animal and only water to the other. Fecal samples were collected at 12, 24 and 48 h after the treatments, plated 2% WA plates and incubated at 25 degrees C for 15 days. A thousand Ancylostoma spp. L-3 larvae Were Spread On these plates. At day 15, infective L-3 recovered from the treated and control groups were counted. In the in vitro test, A. robusta was able to survive the freeze-drying process, grow in the plates, form traps and capture Ancylostoma spp. L-3. There was a 75.38% decrease in the number of infective larvae recovered from the treated group. The in vivo test showed that freeze-dried A. robusta conidia survived the passage through the gastrointestinal tract of the treated dog, was able to grow in the plates and capture Ancylostoma spp. L-3, reducing the number Of recovered L-3 (p < 0.01). Freeze-drying can be an alternative method for conservation of conidia of nematophagous fungi
机译:评价了掠食性真菌强壮型节肢动物(1-31)的冷冻干燥分生孢子的活力以及体外和体内的活性,以防Anthylostoma spp的感染性幼虫(L-3)。在狗里。将罗布斯塔孢子孢子冻干并在4℃下保存一个月。将冷冻干燥的分生孢子稀释至1 x 10(3)分生孢子/ ml,然后进行体内测试。治疗组由含有分生孢子(1 ml)和1000个Ancylostoma spp的溶液组成。将(L-3)放在培养皿中,在25°C的黑暗环境中放置2%的水琼脂(2%的WA),在黑暗中放置10天。对照组由1000个Ancylostoma spp组成。 L-3,镀2%WA。 10天后,Ancylostoma spp。从治疗组和对照组的L-3被回收并计数。通过对一只动物施以单次口服剂量的水溶液中的冷冻干燥分生孢子(1.5 x 10(5)),对另一只动物施以水,对两只狗进行了体内测试。在处理后的12、24和48小时收集粪便样品,铺上2%WA平板,并在25℃下孵育15天。一千个Ancylostoma spp。将L-3幼虫散布在这些板上。在第15天,对从治疗组和对照组中回收的感染性L-3进行计数。在体外测试中,罗布斯芽孢杆菌能够在冷冻干燥过程中存活,在平板中生长,形成陷阱并捕获Ancylostoma spp。 L-3。从治疗组中回收的感染性幼虫数量减少了75.38%。体内试验表明,冷冻干燥的强壮曲霉分生孢子在经过治疗的狗的胃肠道中幸存下来,能够在平板中生长并捕获Ancylostoma spp。 L-3,减少了回收的L-3数量(p <0.01)。冷冻干燥可能是保存线虫真菌分生孢子的另一种方法

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