首页> 外文期刊>Journal of Fish Diseases >In infectious pancreatic necrosis virus carrier Atlantic salmon, Salmo salar L., post-smolts, almost all kidney macrophages ex vivo contain a low level of non-replicating virus
【24h】

In infectious pancreatic necrosis virus carrier Atlantic salmon, Salmo salar L., post-smolts, almost all kidney macrophages ex vivo contain a low level of non-replicating virus

机译:在熏制后的传染性胰腺坏死病毒载体大西洋鲑,鲑鲑中,几乎所有的肾巨噬细胞都含有低水平的非复制型病毒

获取原文
获取原文并翻译 | 示例
           

摘要

The level of infection by infectious pancreatic necrosis virus (IPNV) of kidney macrophages from 12 asymptomatic carrier Atlantic salmon post-smolts was studied. Kidney leucocytes were fractionated on 34/51% Percoll gradients, allowed to adhere to plastic wells overnight, washed to remove non-adherent cells and cultured for up to 7 days with or without renewal of medium on day 3. On day 1, supernatants were harvested, macrophages were counted, lysed and IPNV in the supernatants and lysates was titred in chinook salmon embryo (CHSE-214) cells. The multiplicity of infection ranged between 1:2.2 and 1:7.4 (virus:macrophages). On day 3, the titres of IPNV in macrophage lysates decreased and in wells where the medium was renewed on day 3, IPNV was no longer detectable on day 7. In the supernatants, one fish was positive for IPNV on day 1, four fish on day 3 but none were detectably positive on day 7. In parallel wells in which the medium was not renewed, on day 7 IPNV was detected in macrophage lysates of three fish and the supernatants were also IPNV positive in two of these fish. This suggests that virus might be shed from infected macrophages and then reinfect other macrophages. When macrophages were serially diluted in wells and cultured for 24 h, IPNV could be cultured from macrophage lysates of wells containing between two and 70 macrophages. These results indicate that a very high proportion of the adherent kidney macrophages must be infected with very few non-replicating virions.
机译:研究了来自12只无症状携带者大西洋鲑鱼的肾脏巨噬细胞的传染性胰腺坏死病毒(IPNV)的感染水平。将肾脏白细胞在34/51%Percoll梯度中分级分离,使其在塑料孔中粘附过夜,洗涤以除去不粘附的细胞,并在第3天有或没有更新培养基的情况下培养长达7天。在第1天,收获后,对巨噬细胞进行计数,裂解并将上清液中的IPNV和溶胞产物滴定在chinook鲑鱼胚胎(CHSE-214)细胞中。感染的多样性在1:2.2和1:7.4(病毒:巨噬细胞)之间。在第3天,巨噬细胞裂解物中IPNV的滴度下降,在第3天更新培养基的孔中,在第7天不再检测到IPNV。在上清液中,在第1天,一条鱼IPNV呈阳性。在第3天,但在第7天没有检测到阳性。在没有更新培养基的平行孔中,在第7天,在三只鱼的巨噬细胞裂解物中检测到IPNV,其中两条鱼的上清液也是IPNV阳性。这表明病毒可能会从感染的巨噬细胞中脱落,然后重新感染其他巨噬细胞。将巨噬细胞在孔中连续稀释并培养24小时后,可以从含有2到70个巨噬细胞的孔的巨噬细胞裂解物中培养IPNV。这些结果表明,很大一部分粘附的肾巨噬细胞必须感染很少的非复制性病毒体。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号