Divina B P, Höglund J
College of Veterinary Medicine, University of the Philippines Los Baños College, Laguna, Sweden.
J Helminthol. 2002 Jun;76(2):125-31. doi: 10.1079/JOH2001100.
Eight Swedish Red Breed cattle, about 2 months old, were experimentally infected with a Swedish isolate of Dictyocaulus viviparus (Dviv-Se) from cattle and D. capreolus from roe deer. The aims were to determine whether the roe deer lungworm is infective to cattle or if it can induce seroconversion in cattle against D. viviparus as measured with an ELISA. Four calves which were given 500 Dviv-Se infective larvae (L3) each by larval dosing for two successive days developed patent infection between days 23 and 25 post-inoculation (PI). Larval output varied among the calves and during the patent period. However, maximum recovery occurred between 28 and 56 days PI with peak shedding on day 37 PI. Shedding ceased at day 58 PI and adult worms were recovered from one calf at necropsy (day 67 PI). No immature worms were recovered from the lungs at necropsy. Seroconversion was detected on days 35-42 PI. One Dviv-Se infected calf became seronegative on day 67 PI whereas the other calves still remained seropositive during this period. Prepatency and patency periods of D. viviparus and serological findings in this study basically conform to previous studies. Each calf that was infected with 400 L3 of D. capreolus for two successive days, and about 800 L3 of the same species about 8 weeks later, did not develop to patency based on faecal and post-mortem examinations. Consequently, under the conditions of this study, D. capreolus was not infective to cattle. Two of the four calves that were infected with L3 from roe deer were challenged with L3 cultured from faeces of the Dviv-Se-infected calves. This infection did not develop to patency. Whether this was due to cross-protection as a result of the prior priming with L3 from roe deer is not clear. However, if it is so, it opens up the possibility of using D. capreolus L3 for preventing bovine dictyocauliasis.
八头约2月龄的瑞典红牛被用于实验感染,感染源分别为来自牛的瑞典胎生网尾线虫分离株(Dviv - Se)和来自狍的鹿网尾线虫。目的是确定鹿肺线虫是否能感染牛,或者它是否能像用酶联免疫吸附测定(ELISA)所检测的那样,在牛体内诱导针对胎生网尾线虫的血清转化。四只犊牛连续两天每天经口投服500条Dviv - Se感染性幼虫(L3),在接种后(PI)第23至25天出现显性感染。犊牛之间以及在显性感染期幼虫排出量有所不同。然而,最大排出量出现在接种后28至56天,在接种后第37天达到排出高峰。在接种后第58天排出停止,在尸检时(接种后第67天)从一头犊牛体内回收了成虫。尸检时未从肺中回收未成熟虫体。在接种后第35 - 42天检测到血清转化。一头感染Dviv - Se的犊牛在接种后第67天血清转为阴性,而在此期间其他犊牛仍保持血清阳性。本研究中胎生网尾线虫的潜伏期和显性感染期以及血清学结果基本符合先前的研究。每只连续两天感染400条鹿网尾线虫L3且约8周后感染约800条同一种线虫L3的犊牛,根据粪便和尸检检查未发展为显性感染。因此,在本研究条件下,鹿网尾线虫对牛无感染性。四只感染来自狍的L3的犊牛中有两只受到来自感染Dviv - Se的犊牛粪便中培养的L3的攻击感染。这种感染未发展为显性感染。这是否是由于先前用来自狍的L3进行初次免疫引发的交叉保护尚不清楚。然而,如果是这样,就开启了使用鹿网尾线虫L3预防牛网尾线虫病的可能性。