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Ubiquiter circovirus sequences raise challenges in laboratory diagnosis: The case of honey bee and bee mite, reptiles, and free living amoebae

机译:遍在圆环病毒序列在实验室诊断中提出了挑战:蜜蜂和蜂螨,爬行动物和自由活动的变形虫的情况

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摘要

Circoviruses of pigs and birds are established pathogens, however, the exact role of other, recently described circoviruses and circovirus-like viruses remains to be elucidated. The aim of this study was the detection of circoviruses in neglected host species, including honey bees, exotic reptiles and free-living amoebae by widely used broad-spectrum polymerase chain reaction (PCR) assays specific for the replication initiation protein coding gene of these viruses. The majority of sequences obtained from honey bees were highly similar to canine and porcine circoviruses, or, were distantly related to dragonfly cycloviruses. Other rep sequences detected in some honey bees, reptiles and amoebae showed similarities to various rep sequences deposited in the GenBank. Back-to-back PCR primers designed for the amplification of whole viral genomes failed to work that suggested the existence of integrated rep-like elements in many samples. Rolling circle amplification and exonuclease treatment confirmed the absence of small circular DNA genomes in the specimens analysed. In case of honey bees Varroa mite DNA contamination might be a source of the identified endogenous rep-like elements. The reptile and amoebae rep-like sequences were nearly identical with each other and with sequences detected in chimpanzee feces raising the possibility that detection of novel or unusual rep-like elements in some host species might originate from the microbial community of the host. Our results indicate that attention is needed when broad-spectrum rep gene specific polymerase chain reaction is chosen for laboratory diagnosis of circovirus infections.
机译:猪和鸟的圆环病毒是确定的病原体,但是,尚需阐明其他最近描述的圆环病毒和圆环病毒样病毒的确切作用。这项研究的目的是通过针对这些病毒的复制起始蛋白编码基因的广泛使用的广谱聚合酶链反应(PCR)分析方法,检测被忽视的宿主物种中的圆环病毒,包括蜜蜂,外来爬行动物和自由活动的变形虫。 。从蜜蜂获得的大多数序列与犬和猪圆环病毒高度相似,或者与蜻蜓环病毒远缘相关。在一些蜜蜂,爬行动物和变形虫中检测到的其他rep序列与GenBank中保存的各种rep序列相似。设计用于扩增整个病毒基因组的背对背PCR引物无法工作,这提示许多样品中存在整合的rep-like元件。滚环扩增和核酸外切酶处理证实了所分析的标本中不存在小的环状DNA基因组。在蜜蜂的情况下,螨螨DNA污染可能是已鉴定出的内源性rep-like元素的来源。爬行动物和变形虫的rep-like序列彼此几乎相同,并且在黑猩猩粪便中检测到的序列增加了在某些宿主物种中检测新颖或不寻常的rep-like元素的可能性,可能源自宿主的微生物群落。我们的结果表明,当选择广谱rep基因特异性聚合酶链反应进行圆环病毒感染的实验室诊断时,需要引起注意。

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