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冷冻保存对适应于发育抑制的苯并咪唑抗性捻转血矛线虫分离株的影响。

The influence of cryopreservation on a benzimidazole-resistant isolate of Haemonchus contortus conditioned for inhibited development.

作者信息

Hendrikx W M, Boersema J H, Eysker M

机构信息

Department of Veterinary Helminthology and Entomology, Faculty of Veterinary Medicine, State University Utrecht, The Netherlands.

出版信息

Parasitol Res. 1988;74(6):569-73. doi: 10.1007/BF00531636.

Abstract

Larvae of a fenbendazole (FBZ)-selected, benzimidazole-resistant strain of Haemonchus contortus were conditioned for inhibited development during 7 weeks at 15 degrees C. Sheep raised nearly worm-free were infected with nonfrozen larvae (L3). Larvae from the same batch were exsheathed and cryopreserved over liquid nitrogen for 1 year, and another group of sheep was infected with the same dose of these L3 larvae after thawing. Egg hatch assays for all sheep were done between 21 and 30 days post infection (p.i.). Fenbendazole susceptibility was tested by treating 50% of each group of sheep on day 30 p.i. Worm counts of all sheep were done on day 38 p.i. The exsheathment time of the designated frozen L3 larvae at 15 degrees C exceeded the usual time span at room temperature. Of the frozen L3 larvae, 60% was motile after thawing. The mean LC50 values (micrograms tiabendazole/ml) and the mean percentage of efficacy after FBZ treatment against total worm burden, adults and early L4 larvae of nonfrozen and frozen H. contortus were not significantly different. The mean percentages of take (infectivity) for nonfrozen and frozen doses were 35.3% and 5.9%, respectively (P less than 0.001). In nontreated sheep, the mean percentages of inhibition for nonfrozen and frozen doses were 91.9%, and 54.2%, respectively (P less than 0.01). The exsheathment time seems to be temperature-dependent. The induction of inhibited development of L3 larvae during 7 weeks was as effective as during 5 weeks at 15 degrees C.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

将苯并咪唑抗性捻转血矛线虫(Haemonchus contortus)用芬苯达唑(FBZ)选育出的幼虫在15℃下培养7周,以诱导其发育抑制。将几乎无虫的绵羊感染未冷冻的幼虫(L3)。将同一批次的幼虫脱鞘并在液氮中冷冻保存1年,另一组绵羊在解冻后感染相同剂量的这些L3幼虫。在感染后(p.i.)21至30天对所有绵羊进行虫卵孵化试验。在感染后第30天,对每组绵羊的50%进行芬苯达唑敏感性测试。在感染后第38天对所有绵羊进行虫体计数。指定的冷冻L3幼虫在15℃下的脱鞘时间超过了室温下的正常时间范围。冷冻的L3幼虫解冻后60%仍有活力。未冷冻和冷冻的捻转血矛线虫经FBZ处理后,对总虫负荷、成虫和早期L4幼虫的平均半数致死浓度(噻苯达唑微克/毫升)值和平均药效百分比无显著差异。未冷冻和冷冻剂量的平均感染率分别为35.3%和5.9%(P<0.001)。在未处理的绵羊中,未冷冻和冷冻剂量的平均抑制率分别为91.9%和54.2%(P<0.01)。脱鞘时间似乎与温度有关。在15℃下,7周诱导L3幼虫发育抑制的效果与5周相同。(摘要截短于250字)

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