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新一代测序技术在排除牛白血病病毒作为单峰骆驼成年骆驼白血病病因方面的实用性。

Usefulness of Next-Generation Sequencing in Excluding Bovine Leukemia Virus as a Cause of Adult Camel Leukosis in Dromedaries.

作者信息

Wernery Ulrich, Teng Jade L L, Ma Yuanchao, Kinne Joerg, Yeung Man-Lung, Anas Safna, Lau Susanna K P, Woo Patrick C Y

机构信息

Central Veterinary Research Laboratory, Dubai, United Arab Emirates.

Faculty of Dentistry, The University of Hong Kong, Hong Kong Special Administrative Region, China.

出版信息

Pathogens. 2023 Jul 29;12(8):995. doi: 10.3390/pathogens12080995.

Abstract

Adult camel leukosis is an emerging hematological and neoplastic disease in dromedaries. It has been hypothesized that bovine leukemia virus (BLV) or its genetic variants may be associated with adult camel leukosis. In this study, we used next-generation sequencing (NGS) to detect all possible viruses in five lung samples from five dromedaries with histopathological evidence of adult camel leukosis and four tissue samples from two control dromedaries. A total throughput of 114.7 Gb was achieved, with an average of 12.7 Gb/sample. For each sample, all the pair-end 151-bp reads were filtered to remove rRNA sequences, bacterial genomes and redundant sequences, resulting in 1-7 Gb clean reads, of which <3% matched to viruses. The largest portion of these viral sequences was composed of bacterial phages. About 100-300 reads in each sample matched "multiple sclerosis-associated retrovirus", but manual analysis showed that they were only repetitive sequences commonly present in mammalian genomes. All viral reads were also extracted for analysis, confirming that no BLV or its genetic variants or any other virus was detected in the nine tissue samples. NGS is not only useful for detecting microorganisms associated with infectious diseases, but also important for excluding an infective cause in scenarios where such a possibility is suspected.

摘要

成年骆驼白血病是单峰驼中一种新出现的血液学和肿瘤性疾病。据推测,牛白血病病毒(BLV)或其基因变体可能与成年骆驼白血病有关。在本研究中,我们使用下一代测序(NGS)技术,对来自5只患有成年骆驼白血病组织病理学证据的单峰驼的5份肺样本以及来自2只对照单峰驼的4份组织样本中的所有可能病毒进行检测。总通量达到114.7 Gb,平均每个样本12.7 Gb。对于每个样本,所有双端151 bp的 reads 都经过过滤,以去除rRNA序列、细菌基因组和冗余序列,得到1 - 7 Gb的clean reads,其中与病毒匹配的不到3%。这些病毒序列的最大部分由细菌噬菌体组成。每个样本中约有100 - 300条 reads 与“多发性硬化相关逆转录病毒”匹配,但人工分析表明它们只是哺乳动物基因组中常见的重复序列。所有病毒 reads 也被提取用于分析,证实这9份组织样本中未检测到BLV或其基因变体或任何其他病毒。NGS不仅有助于检测与传染病相关的微生物,在怀疑存在感染性病因的情况下,对于排除感染性病因也很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c1f/10459180/f31fca118866/pathogens-12-00995-g001.jpg

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