Hsu H C, Lo C F, Lin S C, Liu K F, Peng S E, Chang Y S, Chen L L, Liu W J, Kou G H
Department of Zoology, National Taiwan University, Taipei, ROC.
Dis Aquat Organ. 1999 Dec 22;39(1):13-9. doi: 10.3354/dao039013.
We re-tested stored (frozen) DNA samples in 5 independent polymerase chain reaction (PCR) replicates and confirmed that equivocal test results from a previous study on white spot syndrome virus (WSSV) in brooders and their offspring arose because amounts of WSSV DNA in the test samples were near the sensitivity limits of the detection method. Since spawning stress may trigger WSSV replication, we also captured a fresh batch of 45 brooders for WSSV PCR testing before and after spawning. Replicates of their spawned egg batches were also WSSV PCR tested. For these 45 brooders, WSSV prevalence before spawning was 67% (15/45 1-step PCR positive, 15/45 2-step PCR positive and 15/45 2-step PCR negative). Only 27 (60%) spawned successfully. Of the successful spawners, 56% were WSSV PCR positive before spawning and 74% after. Brooders (15) that were heavily infected (i.e. 1-step PCR positive) when captured mostly died within 1 to 4 d, but 3 (20%) did manage to spawn. All their egg batch sub-samples were 1-step PCR positive and many failed to hatch. The remaining 30 shrimp were divided into a lightly infected group (21) and a 2-step PCR negative group (9) based on replicate PCR tests. The spawning rates for these 2 groups were high (81 and 78%, respectively). None of the negative spawners (7) became WSSV positive after spawning and none gave egg samples positive for WSSV. In the lightly infected group (21), 6 brooders were 2-step WSSV PCR negative and 15 were 2-step WSSV PCR positive upon capture. However, all of them were WSSV PCR positive in replicate tests and after spawning or death. Four died without spawning. The remaining 17 spawned but only 2 gave egg samples PCR negative for WSSV. The other 15 gave PCR positive egg samples, but they could be divided into 2 spawner groups: those (7) that became heavily infected (i.e. 1-step PCR positive) after spawning and those (8) that remained lightly infected (i.e. became or remained 2-step PCR positive only). Of the brooders that became heavily infected after spawning, almost all egg sample replicates (91 %) tested 2-step PCR positive. One brooder even gave heavily infected (i.e. 1-step PCR positive) egg samples. For the brooders that remained lightly infected after spawning, only 27% of the egg sample replicates were 2-step PCR positive. Based on these results, we recommend that to avoid false negatives in WSSV PCR brooder tests screening tests should be delayed until after spawning. We also recommend, with our PCR detection system, discarding all egg batches from brooders that are 1-step PCR positive after spawning. On the other hand, it may be possible with appropriate monitoring to use eggs from 2-step PCR positive brooders for production of WSSV-free or lightly infected postlarvae. These may be used to stock shrimp ponds under low-stress rearing conditions.
我们对储存的(冷冻)DNA样本进行了5次独立的聚合酶链反应(PCR)重复检测,证实先前一项关于亲虾及其后代白斑综合征病毒(WSSV)研究中出现的可疑检测结果,是因为检测样本中WSSV DNA的量接近检测方法的灵敏度极限。由于产卵应激可能触发WSSV复制,我们还采集了45只亲虾的新样本,在产卵前后进行WSSV PCR检测。对其产卵批次的重复样本也进行了WSSV PCR检测。对于这45只亲虾,产卵前WSSV患病率为67%(15/45一步法PCR阳性,15/45两步法PCR阳性,15/45两步法PCR阴性)。只有27只(60%)成功产卵。在成功产卵的亲虾中,产卵前56%的WSSV PCR呈阳性,产卵后74%呈阳性。捕获时严重感染(即一步法PCR阳性)的亲虾(15只)大多在1至4天内死亡,但有3只(20%)成功产卵。它们所有的卵批次子样本一步法PCR均呈阳性,且许多未能孵化。根据重复PCR检测,其余30只虾分为轻度感染组(21只)和两步法PCR阴性组(9只)。这两组的产卵率都很高(分别为81%和78%)。所有阴性产卵亲虾(7只)在产卵后均未变为WSSV阳性,且没有提供WSSV呈阳性的卵样本。在轻度感染组(21只)中,6只亲虾捕获时两步法WSSV PCR呈阴性,15只呈阳性。然而,它们在重复检测以及产卵或死亡后所有WSSV PCR均呈阳性。4只未产卵就死亡。其余17只产卵,但只有2只提供的卵样本WSSV PCR呈阴性。另外15只提供的卵样本PCR呈阳性,但可分为2个产卵亲虾组:产卵后严重感染(即一步法PCR阳性)的亲虾(7只)和仍轻度感染(即仅变为或仍为两步法PCR阳性)的亲虾(8只)。在产卵后严重感染的亲虾中,几乎所有卵样本重复检测(91%)两步法PCR呈阳性。有1只亲虾甚至提供了严重感染(即一步法PCR阳性)的卵样本。对于产卵后仍轻度感染的亲虾,只有27%的卵样本重复检测两步法PCR呈阳性。基于这些结果,我们建议为避免WSSV PCR亲虾检测出现假阴性,筛查检测应推迟至产卵后进行。我们还建议,使用我们的PCR检测系统时,应丢弃产卵后一步法PCR呈阳性亲虾的所有卵批次。另一方面,通过适当监测,有可能使用两步法PCR呈阳性亲虾的卵来生产无WSSV或轻度感染的后期幼体。这些后期幼体可用于在低应激养殖条件下放养虾塘。