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对一株2024年从哈萨克斯坦阿拉木图地区分离出的绵羊痘病毒进行系统发育分析,并研究其对美利奴羊的致病性。

Phylogenetic analysis of a 2024 Sheeppox virus isolate from the Almaty region of Kazakhstan and investigation of its pathogenicity in merino sheep.

作者信息

Azanbekova Moldir, Mambetaliyev Muratbay, Valiyeva Aisulu, Kozhabergenov Nurlan, Aldayarov Nurbek, Kilibayev Sanat, Usserbayev Bekbolat, Tuyskanova Moldir, Kadyrova Balziya, Myrzakhmetova Balzhan, Kutumbetov Lespek, Chervyakova Olga, Nurabayev Sergazy, Berdikulov Maxat, Kerimbayev Aslan, Rsaliyev Aralbek, Abduraimov Yergali, Zhugunissov Kuandyk

机构信息

Research Institute for Biological Safety Problems, National Holding "QazBioPharm", Guardeyskiy, Kazakhstan.

Kyrgyz-Turkish Manas University, Bishkek, Kyrgyzstan.

出版信息

Front Vet Sci. 2025 Jul 21;12:1623187. doi: 10.3389/fvets.2025.1623187. eCollection 2025.

Abstract

INTRODUCTION

Sheeppox virus (SPPV) is a significant pathogen that affects small ruminants and causes substantial economic losses. It is essential to perform detailed molecular and pathogenic characterization of field isolates to control the disease and develop prevention strategies.

METHODS

The SPPV isolate "Sheeppox/KZ/Targap/2024" was obtained in 2024 from a diseased lamb during an outbreak in Targap village in the Almaty region of Kazakhstan. The isolate was passaged three times in lamb kidney-cell culture, and the 50% tissue culture infectious dose (TCID) assay indicated a titer of 5.33 ± 0.08 log TCID/mL. Identification was performed using polymerase chain reaction (PCR) and whole-genome sequencing, and the complete genome was submitted to GenBank (accession number PV434148). Experimental infection studies were conducted with Merino sheep.

RESULTS

The virus activity was 4.75 ± 0.02 log ID/mL. The virus neutralization test showed 100% seroconversion by day 9 post-infection and maximum antibody titers (1:32) by day 21. ELISA confirmed that there was a strong immune response (>90% seropositivity). PCR detected viral DNA by day 5 post-infection in most tissues. Necropsy revealed typical pathological sheeppox lesions in the lungs, spleen, lymph nodes, and skin. Histopathological analysis demonstrated acute-stage features including massive cellular infiltration, vasculitis, edema, and pox lesions.

CONCLUSION

The findings confirm previously known characteristics of SPPV and provide new insights into the molecular and pathogenic properties of the "Sheeppox/KZ/Targap/2024" isolate.

摘要

引言

绵羊痘病毒(SPPV)是一种影响小型反刍动物并造成重大经济损失的重要病原体。对野外分离株进行详细的分子和致病性特征分析对于控制该疾病和制定预防策略至关重要。

方法

2024年,在哈萨克斯坦阿拉木图地区塔尔加普村的一次疫情中,从一只患病羔羊身上获得了绵羊痘病毒分离株“绵羊痘/KZ/塔尔加普/2024”。该分离株在羔羊肾细胞培养物中传代三次,50%组织培养感染剂量(TCID)测定表明滴度为5.33±0.08 log TCID/mL。使用聚合酶链反应(PCR)和全基因组测序进行鉴定,并将完整基因组提交至GenBank(登录号PV434148)。用美利奴绵羊进行了实验性感染研究。

结果

病毒活性为4.75±0.02 log ID/mL。病毒中和试验显示感染后第9天血清转化率达100%,第21天抗体滴度最高(1:32)。酶联免疫吸附测定(ELISA)证实存在强烈的免疫反应(血清阳性率>90%)。PCR在感染后第5天在大多数组织中检测到病毒DNA。尸检显示肺、脾、淋巴结和皮肤出现典型的绵羊痘病理损伤。组织病理学分析显示急性期特征,包括大量细胞浸润、血管炎、水肿和痘疹病变。

结论

这些发现证实了绵羊痘病毒先前已知的特征,并为“绵羊痘/KZ/塔尔加普/2024”分离株的分子和致病特性提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37dd/12319417/12b26096cc51/fvets-12-1623187-g001.jpg

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