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摩洛哥新生腹泻犊牛中A组轮状病毒的分离与鉴定

Isolation and identification of group A rotaviruses among neonatal diarrheic calves, Morocco.

作者信息

Ennima Imane, Sebbar Ghizlane, Harif Bachir, Amzazi Saaid, Loutfi Chafiqa, Touil Nadia

机构信息

Laboratory of Biochemistry and Immunology, Department of Biology, Faculty of Sciences, 4 Avenue Ibn Batouta, B.P. 1014 RP, Rabat, Morocco.

Société de Productions des Produits Biologiques & Vétérinaires, Avenue Hassan II, 10051, Rabat, Morocco.

出版信息

BMC Res Notes. 2016 May 5;9:261. doi: 10.1186/s13104-016-2065-8.

Abstract

BACKGROUND

Group A rotaviruses (RVA) are the main cause of neonatal calve diarrhea (NCD) in Morocco. In this study, we isolated RVA strains from NCD clinical samples in order to support RVA disease control in Morocco. This isolation process constitutes a first step toward vaccine development.

METHODS

Thirteen fecal samples were obtained from calves with a single episode of neonate calf diarrhea at three different dairies and two samples were collected from field during a severe NCD outbreak. Diagnosis of RVA infection was based on fecal immune-chromatographic rapid test and further evaluated for their hemagglutination (HA) activity. RVA isolation was carried out on MA104 cells after inoculates were treated with different concentrations of trypsin TPCK. All RVA isolates were confirmed by LSI VetMAX™ Triplex Ruminant Rotavirus & Coronavirus Real-Time PCR kit. G and P typing were determined by direct sequencing of the VP4 and VP7 amplicons.

RESULTS

RVA isolation was achieved for nine clinical samples following one or two passages (60 %) and was properly depended on HA activity and trypsin treatment of inoculates. The first sign of CPE detected consisted of increased cell granularity, obscure cell boundaries, cell rounding, and eventual degeneration and detachment of cells. At lower TPCK concentration (3-10 μg/inoculum), no changes at the cellular level were observed, while cells activated with 25-30 μg of trypsin/inoculums, they degenerated and trypsin cytotoxicity was enhanced. Appreciable changes in cell's morphology were detected with optimal trypsin concentration of 15-20 μg trypsin/inoculums. Data from qRT-PCR confirmed that unsuccessful cultivations have No-Ct, and all nine isolates have Ct values ranged between 12.17 and 24.69. Analysis sequencing revealed that field isolates were of G6 P[5] serotype and isolates from the dairy NCD samples were of G10 P[14] serotype.

CONCLUSIONS

To our knowledge, this is the first study in Morocco which reports the circulation of G10P[14] in NCD on dairy farms and G6P[5] in the field. Our study constitutes a crucial and a necessary step allowing preventive and veterinary medicine to support RVA disease controls in the country.

摘要

背景

A 组轮状病毒(RVA)是摩洛哥新生犊牛腹泻(NCD)的主要病因。在本研究中,我们从 NCD 临床样本中分离出 RVA 毒株,以支持摩洛哥的 RVA 疾病防控。这一分离过程是疫苗研发的第一步。

方法

从三个不同奶牛场的犊牛单次发生新生犊牛腹泻时采集了 13 份粪便样本,并在一次严重的 NCD 疫情期间从现场采集了 2 份样本。RVA 感染的诊断基于粪便免疫层析快速检测,并进一步评估其血凝(HA)活性。在用不同浓度的胰蛋白酶 TPCK 处理接种物后,在 MA104 细胞上进行 RVA 分离。所有 RVA 分离株均通过 LSI VetMAX™ 三重反刍动物轮状病毒和冠状病毒实时 PCR 试剂盒进行确认。G 和 P 分型通过对 VP4 和 VP7 扩增子进行直接测序来确定。

结果

9 份临床样本在传代一或两次后成功分离出 RVA(60%),且这恰取决于 HA 活性和对接种物的胰蛋白酶处理。检测到的 CPE 的首个迹象包括细胞颗粒度增加、细胞边界模糊、细胞变圆以及最终细胞变性和脱落。在较低的 TPCK 浓度(3 - 10μg/接种物)下,未观察到细胞水平的变化,而用 25 - 30μg 胰蛋白酶/接种物激活细胞时,细胞会变性且胰蛋白酶细胞毒性增强。在胰蛋白酶最佳浓度为 15 - 20μg 胰蛋白酶/接种物时,检测到细胞形态有明显变化。qRT - PCR 数据证实未成功培养的样本无 Ct 值,所有 9 个分离株的 Ct 值在 12.17 至 24.69 之间。序列分析显示,现场分离株为 G6P[5]血清型奶牛场 NCD 样本分离株为 G10P[14]血清型。

结论

据我们所知,这是摩洛哥首次报告奶牛场 NCD 中 G10P[14]的流行情况以及现场 G6P[5]的流行情况的研究。我们的研究是至关重要且必要的一步,有助于预防医学和兽医学支持该国的 RVA 疾病防控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bb5/4858901/a8860c303a59/13104_2016_2065_Fig1_HTML.jpg

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