Departamento de Veterinária, Universidade Federal de Viçosa, P. H. Rolfs, Viçosa-MG CEP 3657000, Brazil.
Vet Parasitol. 2011 Mar 10;176(2-3):236-9. doi: 10.1016/j.vetpar.2010.10.051. Epub 2010 Nov 4.
Viability and in vitro and in vivo activities of freeze-dried conidia of the predatory fungus Arthrobotrys robusta (I-31) were evaluated against infective larvae (L(3)) of Ancylostoma spp. in dogs. A. robusta conidia were lyophilized and stored at 4°C for a month. Freeze-dried conidia were diluted to 1×10(3)conidia/ml and tested in vivo. The treated group consisted of a solution containing conidia (1ml) and 1000 Ancylostoma spp. (L(3)) placed on Petri dishes plated with 2% water-agar (2% WA), at 25°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 (1.5×10(5)) in aqueous solution to one animal and only water to the other. Fecal samples were collected at 12, 24 and 48h after the treatments, plated 2% WA plates and incubated at 25°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.
本文评估了冷冻干燥捕食真菌节丛孢(Arthrobotrys robusta)(I-31)分生孢子的活力及其在体外和体内对犬类感染性幼虫(L(3))的活性。将节丛孢分生孢子冻干并在 4°C 下储存一个月。将冻干的分生孢子稀释至 1×10(3)个孢子/ml 并进行体内测试。实验组由含有分生孢子(1ml)和 1000 条旋毛虫(L(3))的溶液组成,将其置于铺有 2%水琼脂(2%WA)的培养皿中,在 25°C、黑暗条件下培养 10 天。对照组由 1000 条旋毛虫 L(3)组成,铺在 2% WA 上。10 天后,从实验组和对照组中回收并计数旋毛虫 L(3)。在体内试验中,将冻干分生孢子(1.5×10(5))的水溶液以单口服剂量施用于一只动物,而另一只动物仅给予水。在处理后 12、24 和 48 小时收集粪便样本,接种在 2% WA 平板上,并在 25°C 下孵育 15 天。在这些平板上散布 1000 条旋毛虫 L(3)幼虫。第 15 天,从实验组和对照组中回收的感染性 L(3)进行计数。在体外试验中,节丛孢能够在冷冻干燥过程中存活,在平板上生长,形成陷阱并捕获旋毛虫 L(3)。实验组中回收的感染性幼虫数量减少了 75.38%。体内试验表明,冻干的节丛孢分生孢子能够通过治疗犬的胃肠道,在平板上生长并捕获旋毛虫 L(3),从而减少回收的 L(3)数量(p<0.01)。冷冻干燥可能是保存食线虫真菌分生孢子的一种替代方法。