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卷尾猴新病毒:慢性HBV的动物模型? [复制链接]

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发表于 2018-6-20 14:30 |只看该作者 |倒序浏览 |打印
New Virus in Capuchin Monkeys: Animal Model for Chronic HBV?
                                                                                         
                                            
                    
                                            
                    
                                            
                    
                                            
                    
                                            
                    
                                            
                    
                                       
The discovery of a new hepatitis B virus in capuchin monkeys could be important in guiding future work to investigate the pathogenesis of HBV infection and potential cures for its chronic infection.
By Nicola M. Parry, BVSc, MRCVS, MSc, DACVP, ELS
“The identification of a novel primate hepadnavirus offers new perspectives for urgently needed animal models of chronic hepatitis B,” wrote Breno Frederico de Carvalho Dominguez Souza, from the University of Bonn Medical Centre in Germany, and colleagues, in a recent study published in the Journal of Hepatology.

According to the authors, hepatitis B virus (HBV) commonly infects humans. Chronic infection can have serious complications, including cirrhosis and liver cancer, which cause at least 680,000 deaths worldwide each year.

Chronic HBV thus remains a major public health issue with no effective cure. And, despite recent advances in understanding HBV infection, research to investigate potential cures remain stalled by the lack of suitable animal models for chronic HBV infection.

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HBV, which belongs to the genus Orthohepadnavirus in the family Hepadnaviridae, is divided into 10 genotypes (A-J) in humans. And, while additional genotypes infect Old World monkeys such as chimpanzees, gorillas, orangutans, and gibbons, no evidence exists to suggest that these monkey genotypes can infect humans.

In addition to HBV, woolly monkey HBV is the only other hepadnavirus known to infect nonhuman primates, and only a paucity of data exist on HBV in New World species.

With this in mind, Souza and colleagues conducted a study in which they screened New World monkeys in Brazil for hepadnaviruses.

Using molecular and serologic tests, they screened sera from 124 New World monkeys belonging to at least 10 different species. Most of the animals screened were capuchin monkeys (N = 95).

In their study, Souza and colleagues identified a new species of HBV in capuchin monkeys, which they named capuchin monkey HBV (CMHBV). “We found CMHBV-specific antibodies in five animals and high CMHBV concentrations in one animal,” they wrote.

According to the researchers, the 5 monkeys that were antibody positive appeared healthy. One other monkey tested positive for hepadnavirus DNA by polymerase chain reaction assay. This animal was thin, lethargic, and mildly dehydrated, they noted, and died 6 months after sampling. However, because no additional samples were provided after the monkey’s death, the researchers were unable to determine whether its clinical signs were related to CMHBV infection.

Nevertheless, the virus in this case had an intact preCore domain, the authors noted. This domain is responsible for production of hepadnaviral e-antigen, which is a key viral protein involved in establishing chronic HBV infection. As a consequence, the researchers hypothesized the existence of chronic infection in the hepadnavirus DNA-positive monkey. And, if CMHBV can cause chronic infection, CMHBV-infected animals could serve as new animal models for chronic HBV infection in humans, they said.

In the laboratory, the researchers found that the new virus produced infection patterns similar to those of HBV. It also infected human liver cells using the same receptor that HBV uses, leading the authors to suggest a zoonotic potential for hepadnaviruses circulating in New World monkeys.

“However, infection experiments relying on full hepadnaviruses and primary human liver cells will be required to permit definite conclusions on the zoonotic potential of CMHBV,” they stressed.

And, when they performed evolutionary analyses on CMHBV, Souza and colleagues found information that helped to explain the general evolution of hepadnaviruses in primates. Their findings suggested that primates began carrying hepadnaviruses millions of years ago. In particular, the origins of HBV-related viruses may date back to African ancestors of New World monkeys at that time, they said, when these animals entered South America during its transatlantic colonization.

The researchers also found a link between HBV and hominoid ancestors, including humans and apes, leading them to suggest that the origins of HBV date back to before modern humans even evolved.

“Our results elucidate the evolutionary origins and dispersal of primate HBV, identify a new orthohepadnavirus reservoir, and enable new perspectives for animal models of hepatitis B,” Souza and colleagues concluded.


Dr. Parry, a board-certified veterinary pathologist, graduated from the University of Liverpool in 1997. After 13 years in academia, she founded Midwest Veterinary Pathology, LLC, where she now works as a private consultant. Dr. Parry writes regularly for veterinary organizations and publications.

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发表于 2018-6-20 14:30 |只看该作者
卷尾猴新病毒:慢性HBV的动物模型?
在卷尾猴中发现新的乙型肝炎病毒可能对指导未来的工作以调查HBV感染的发病机制和潜在的慢性感染治疗非常重要。
Nicola M. Parry,BVSc,MRCVS,MSc,DACVP,ELS
来自德国波恩大学医学中心的Breno Frederico de Carvalho Dominguez Souza及其同事在最近发表的一项研究中写道:“新型灵长类肝炎病毒的鉴定为迫切需要的慢性乙型肝炎动物模型提供了新的视角。肝胆外科杂志。

据作者称,乙型肝炎病毒(HBV)通常会感染人类。慢性感染可以有严重的并发症,包括肝硬化和肝癌,每年至少导致680,000人死亡。

因此慢性HBV仍然是一个重大的公共卫生问题,没有有效的治疗方法。尽管近期HBV病毒感染的研究取得了进展,但由于缺乏合适的慢性HBV感染动物模型,研究潜在治疗的研究仍然停滞不前。

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属于嗜肝DNA病毒科的属于Orthohepadnavirus属的HBV在人体内被分成10种基因型(A-J)。而且,虽然其他基因型感染了旧世界的猴子,如黑猩猩,大猩猩,猩猩和长臂猿,但没有证据表明这些猴基因型可以感染人类。

除HBV外,羊毛猴HBV是已知感染非人灵长类动物的唯一其他嗜肝DNA病毒,并且在新世界物种中仅存在少量HBV数据。

考虑到这一点,Souza及其同事进行了一项研究,他们在巴西为新发现的嗜肝DNA病毒筛选了新世界猴。

利用分子和血清学试验,他们筛选了来自至少10种不同物种的124只新世界猴的血清。大多数筛选的动物是卷尾猴(N = 95)。

在他们的研究中,Souza及其同事在卷尾猴中鉴定出一种新的HBV种类,他们命名为卷尾猴HBV(CMHBV)。 “我们在五只动物中发现了CMHBV特异性抗体,在一只动物中发现了高CMHBV浓度,”他们写道。

据研究人员介绍,抗体阳性的5只猴子看起来健康。另一只猴子通过聚合酶链式反应试验测试了嗜肝DNA病毒DNA阳性。他们指出,这种动物很薄,昏昏沉沉,并且轻度脱水,并在取样后6个月死亡。然而,由于在猴死后没有提供额外的样本,研究人员无法确定其临床体征是否与CMHBV感染有关。

尽管如此,作者指出,在这种情况下,病毒拥有完整的preCore域。该结构域负责产生嗜肝DNA病毒e抗原,它是一种参与建立慢性HBV感染的关键病毒蛋白。因此,研究人员假设嗜肝DNA病毒DNA阳性猴子存在慢性感染。他们说,如果CMHBV可引起慢性感染,那么CMHBV感染的动物可以作为人类慢性HBV感染的新动物模型。

在实验室中,研究人员发现新病毒产生的感染模式与HBV相似。它还使用与HBV使用的受体相同的受体感染人类肝细胞,这使得作者提出了在新世界猴中循环的嗜肝DNA病毒的动物传染病潜力。

“但是,依靠完整的肝炎病毒和原发性人类肝细胞进行感染实验将需要对CMHBV的动物传染病潜力给出明确的结论,”他们强调。

而且,当他们对CMHBV进行进化分析时,Souza及其同事发现有助于解释灵长类动物嗜肝DNA病毒一般进化的信息。他们的研究结果表明灵长类动物在数百万年前开始携带肝炎病毒。他们说,当这些动物在其跨大西洋殖民时期进入南美洲时,HBV相关病毒的起源可以追溯到当时新大陆的非洲祖先。

研究人员还发现了HBV与包括人类和猿类在内的类猿祖先之间的联系,从而导致他们认为,HBV的起源可以追溯到现代人甚至还未发展之前。

“我们的研究结果阐明了灵长类动物HBV的进化起源和扩散,确定了一个新的正交脑热病毒储库,并为乙型肝炎动物模型提供了新的观点,”Souza及其同事得出结论。

  Parry博士,董事会认证的兽医病理学家,1997年毕业于利物浦大学。在学术界工作13年后,她创立了中西部兽医病理学有限责任公司,现在她担任私人顾问。帕里博士定期为兽医组织和出版物撰稿。
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