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Reemergence of Ebola in 2021 2021年再次出现埃博拉病毒
Pub Date : 2022-01-01 DOI: 10.16966/2473-1846.168
Tseha St
Ebola also known as Ebola Virus Disease (EVD) is a serious disease that is caused by viruses that belong to the genus Ebola virus (EBOV). The purpose of this review is to discuss the most recent Ebola outbreak in Africa. A latest report on Ebola indicated that the disease recently resurged in Democratic Republic of Congo in February 2021. The Democratic Republic of Congo contains heavy forested areas that have been suggested as the primary factor for the repeated outbreaks of Ebola in the Democratic Republic of Congo. In addition to this, consumption of bushmeat and deforestation has been reported as additional factors that have contributed for the repeated Ebola outbreaks in the Democratic Republic of Congo. The most recent Ebola outbreak that was documented in Democratic Republic of Congo in 2021 might be due to transmission of the EBOV from Ebola survivor. Therefore, the community in Ebola endemic areas has to be educated as contact with fruit bat, deforestation, consumption of bushmeat and contact with body fluids of Ebola patients are the key ways of transmission of Ebola virus. Moreover, immunization of those at highrisk of being infected by the virus can be taken as an additional measures so as to prevent future outbreaks of Ebola. Furthermore, active surveillance and follow up of survivors of Ebola is needed.
埃博拉也被称为埃博拉病毒病(EVD),是一种由属于埃博拉病毒属(EBOV)的病毒引起的严重疾病。本综述的目的是讨论最近在非洲爆发的埃博拉疫情。一份关于埃博拉病毒的最新报告表明,该疾病最近于2021年2月在刚果民主共和国卷土重来。刚果民主共和国拥有茂密的森林地区,这被认为是刚果民主共和国反复爆发埃博拉疫情的主要因素。除此之外,据报告,食用丛林肉和砍伐森林是导致刚果民主共和国一再爆发埃博拉疫情的其他因素。2021年在刚果民主共和国记录的最近一次埃博拉疫情可能是由于埃博拉幸存者传播的埃博拉病毒。因此,必须对埃博拉流行地区的社区进行教育,因为接触果蝠、砍伐森林、食用丛林肉和接触埃博拉患者的体液是埃博拉病毒传播的主要途径。此外,可以对感染该病毒的高危人群进行免疫接种,作为一项额外措施,以防止未来埃博拉疫情的爆发。此外,需要对埃博拉幸存者进行积极监测和随访。
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引用次数: 0
Hyper-Variable Spike Protein of Omicron Corona Virus and Its Differences with Alpha and Delta Variants: Prospects of RT-PCR and New Vaccine 组粒冠病毒高变刺突蛋白及其与α和δ变异的差异:RT-PCR和新疫苗的前景
Pub Date : 2022-01-01 DOI: 10.16966/2473-1846.166
Chakraborty Ak
NCBI SARS-CoV-2 Database was analyzed between November-December, 2021 to decipher the spread of Delta corona virus variants in the USA and compared with highly transmissible new omicron variant recently originated in South Africa. Presently, B.1.617.2 and AY.103 lineages Delta variants with spike protein L452R, T478K, P681R mutations and F157/R158 two amino acids deletions were predominant in the USA and superseded the deadly outbreaks of B.1.1.7 Alpha variant with deletions of H69, V70 and Y145 amino acids as well as N501Y, and D614G highly transmissible mutations. Interestingly, omicron variant has six H69, V70, V143, Y144, Y145, L212 immune-escape deletions as well as 29 mutations in the spike protein including most deadly N501Y (Y498 in omicron) and D614G (G611 in omicron). This indicated that omicron variant was originated by combination among B.1.1.7, AY.X and B.1.617.2 lineages. A unique three amino acids (EPE) insertion at 215 position of spike protein was detected to compensate six deletions suggesting further recombination events. Three Serine residues were mutated at amino acids 371 (S=L, L368 in omicron), 373 (S=P, P370 in Omicron), 375 (S=F, F372 in omicron) but compensated at 446 (G=S, S443 in omicron) and 496 (G=S, S493 in omicron) at the RBD domain of omicron virus. The three amino acids (ERS) deletion at position 30 in the N-protein acts as another signature of omicron virus. Omicron variant has less mutation in the 2/3 5’-end of the genome that codes for ORF1ab poly-protein but dominant P4715L mutation in the RNA-dependent RNA polymerase. However, overall amino acid composition, alipathic index, and instability index were found fairly constant although hydrophobic plot gave some difference between spike protein of Wuhan and omicron corona viruses. BLAST search detected 20nt and 19nt perfect match of hyper-variable 22957-22977nt region comprising 488-493 amino acids (NH2-PLRSYS-CO2H) of the spike protein of omicron virus with the ch-2 of Seladonia tumulorum or ch-16 of Steromphala cineraria respectively. A primer set designed from the RBD domain of spike gene did not detected the omicron genome by BLAST search but primers from the constant regions of the genome worked well. Such hyper-variation in the spike protein suggested that DNA vaccine or mRNA vaccine using spike gene of corona virus may not efficiently protect omicron virus infection and attenuated whole corona virus vaccine will be safer vaccine.
分析了2021年11月至12月NCBI SARS-CoV-2数据库,以破译Delta冠状病毒变体在美国的传播,并与最近起源于南非的高传染性新组粒变体进行了比较。目前,具有刺突蛋白L452R、T478K、P681R突变和F157/R158两个氨基酸缺失的B.1.1.7 α突变以及N501Y和D614G高传染性突变在美国占主导地位,取代了致命的爆发。有趣的是,组粒变体具有6个H69, V70, V143, Y144, Y145, L212免疫逃逸缺失以及刺突蛋白的29个突变,包括最致命的N501Y(组粒中的Y498)和D614G(组粒中的G611)。这表明组粒变异是由B.1.1.7和AY组合而成的。X和B.1.617.2血统。在刺突蛋白的215个位置检测到一个独特的3个氨基酸(EPE)插入,以弥补6个缺失,表明进一步的重组事件。三个丝氨酸残基在组粒病毒RBD结构域的371 (S=L, L368)、373 (S=P, P370)、375 (S=F, F372)氨基酸上发生突变,但在446 (G=S, S443)和496 (G=S, S493)氨基酸上得到补偿。n蛋白第30位3个氨基酸(ERS)缺失是组粒病毒的另一个特征。Omicron变体在编码ORF1ab多蛋白的基因组2/3 5 '端突变较少,但在RNA依赖的RNA聚合酶中P4715L突变占主导地位。尽管疏水性图显示武汉冠状病毒和组粒冠状病毒刺突蛋白存在一定差异,但总体氨基酸组成、脂溶性指数和不稳定性指数基本不变。BLAST搜索结果显示,组粒病毒刺突蛋白含有488 ~ 493个氨基酸(NH2-PLRSYS-CO2H)的高变量22957 ~ 22977nt区分别与黄花鸡的ch-2区和黄鸡的ch-16区有20个和19个完全匹配。从刺突基因的RBD区域设计的引物无法通过BLAST搜索检测到组粒基因组,但从基因组的恒定区域设计的引物效果良好。刺突蛋白的高度变异表明,利用冠状病毒刺突基因的DNA疫苗或mRNA疫苗可能不能有效地保护组粒病毒感染,减毒全冠病毒疫苗将是更安全的疫苗。
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引用次数: 0
Emergence of Human Avian-Influenza 人类禽流感的出现
Pub Date : 2022-01-01 DOI: 10.16966/2473-1846.169
Tseha St
Emerging viral diseases have become major public health problem in the World. Human-avian influenza is one of emerging viral diseases that significantly contribute to the global burden of respiratory diseases. The objective of this review was to discuss the most recent human-avian influenza outbreak documented in 2021. On basis of their epidemiological features, influenza in humans can be classified as seasonal influenza, pandemic influenza and human-avian influenza. Influenza in humans that are caused by avian influenza viruses which are transmitted across species to humans is known as human-avian influenza. So far, three avian influenza viruses have been recognized to cause human-avian influenza, namely, Asian H7N9 viruses, H5N1 viruses and H5N8. The most recent human-avian influenza outbreak was caused by H5N8, which was documented on February 2021 in Russia. The outbreak was associated with contact with H5N8 infected domestic birds. As the influenza viruses constantly evolve, there is possibility of global outbreak of the disease. Thus, it is necessary to take preparedness actions to counter pandemic threats as they are identified.
新出现的病毒性疾病已成为世界上主要的公共卫生问题。人禽流感是一种新出现的病毒性疾病,严重造成全球呼吸道疾病负担。本次审查的目的是讨论2021年记录的最近一次人类禽流感疫情。根据其流行病学特征,人类流感可分为季节性流感、大流行性流感和人禽流感。由跨物种传播给人类的禽流感病毒引起的人类流感称为人禽流感。到目前为止,已经确认有三种禽流感病毒可引起人类禽流感,即亚洲H7N9病毒、H5N1病毒和H5N8病毒。最近的人类禽流感疫情是由H5N8引起的,于2021年2月在俄罗斯记录在案。此次暴发与接触受H5N8感染的家禽有关。随着流感病毒的不断进化,有可能在全球爆发。因此,有必要采取防备行动,在发现大流行威胁时予以应对。
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引用次数: 0
Comparison of Disease Nature of MERS, SARS-CoV-1, and SARS-CoV-2: A Review MERS、SARS-CoV-1和SARS-CoV-2疾病性质比较研究进展
Pub Date : 2021-01-01 DOI: 10.16966/2473-1846.163
E. S., Sacre Y, Barbour Ek, K. T., A. G., K. W., D. M., Farah D
Background: The lockdown imposed during the waves of SARS-CoV-2, also known as COVID-19, had several consequences on nations at many levels including economic, sociocultural, health and political. The vast majority of countries have been profoundly impacted, despite the widespread of vaccination initiatives all over the countries. With lockdowns still imposed on some European and west Asian countries, it’s still unknown how long SARS-CoV-2 will carry on with its burden on society. The future is indefinite.
背景:在SARS-CoV-2(也称为COVID-19)浪潮期间实施的封锁在经济、社会文化、卫生和政治等多个层面上对各国产生了多种影响。尽管疫苗接种行动在各国广泛开展,但绝大多数国家仍受到了深刻影响。由于一些欧洲和西亚国家仍在实施封锁,目前尚不清楚SARS-CoV-2会给社会带来多长时间的负担。未来是不确定的。
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引用次数: 0
Transcutaneous Vagus Nerve Stimulation is Associated with Lower Mechanical Ventilation and Mortality in COVID-19 Patients 经皮迷走神经刺激与COVID-19患者低机械通气和死亡率相关
Pub Date : 2021-01-01 DOI: 10.16966/2473-1846.165
Nemechek P, A. G., Braida A
Objective: Evaluate the safety and efficacy of transcutaneous vagus nerve stimulation in preventing respiratory failure and improving survival in hospitalized COVID-19 patients.
目的:评价经皮迷走神经刺激预防新冠肺炎住院患者呼吸衰竭和提高生存率的安全性和有效性。
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引用次数: 1
Bayesian Model for Covid-19 to Achieve Immunity by Parsimony of Exponential Functions Minimizing the Inoculum 利用指数函数简约最小化接种量实现Covid-19免疫的贝叶斯模型
Pub Date : 2021-01-01 DOI: 10.16966/2473-1846.160
Lamothe N, Lamothe M, Lamothe D, Sierra C, Gonzalez Ch, Rodas Vh, Lamothe A, Sanchez-Montiel J, Lamothe C, Galicia H, Perez-Avalos Jl, R. O, Cazarin Z, Pena Avdl, Diaz-del Bosque A, Lamothe Pj
A ribonucleoside analog MK-4482/EIDD-2801 blocks SARS-CoV-2 transmission in ferrets and might be able to diminish transmission until vaccineinduced or naturally acquired protective herd immunity is reached [1]. As skinner pointed out, behavioral problems have to be solved through behavioral engineering [2]. Cybernetics has full application in the present condition. As in alcohol consumption, smoking, drugs, gun crimes, wars, and sexually acquired diseases, the teleological Aristotelian causes are not tobacco, drugs, and any other issue, but the aberrant behavior. The situation is not trivial and involves non-classic logic and other mathematical logics [3,4]. The neural topography corresponds to the nucleus accumbens. The latter is the battlefield, and the subject’s obsession is the rise of the neurotransmitter dopamine [3,4]. In general, people are very demanding from their governments; nevertheless, at the same time, they are deeply tolerant with their aberrant behavior promoting the dissemination of the SARSCoV-2 [4,5]. This paper examines how to deal with this problem from a scientific perspective, considering probability methods and classical and doxastic logic, using the Parsimony Principle aiming to reach immunity by minimizing the inoculum.
核糖核苷类似物MK-4482/EIDD-2801阻断SARS-CoV-2在雪貂中的传播,并且可能能够减少传播,直到疫苗诱导或自然获得的保护性群体免疫达到100。正如斯金纳所指出的,行为问题必须通过行为工程来解决。控制论在当前条件下有充分的应用。正如饮酒、吸烟、吸毒、持枪犯罪、战争和性获得性疾病一样,亚里士多德的目的论原因不是烟草、毒品和任何其他问题,而是异常行为。这种情况并不简单,涉及非经典逻辑和其他数学逻辑[3,4]。神经地形图对应伏隔核。后者是战场,受试者的执魔是神经递质多巴胺的上升[3,4]。一般来说,人们对政府的要求很高;然而,与此同时,他们对自己促进SARSCoV-2传播的异常行为却非常宽容[4,5]。本文从科学的角度出发,综合运用概率方法和经典与随机逻辑,运用以最小接种量达到免疫为目的的简约原则,探讨如何处理这一问题。
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引用次数: 1
Prospect of Ion Channel Inhibitors and Cholesterol Lowering Drugs to Combat COVID-19 离子通道抑制剂和降胆固醇药物对抗COVID-19的前景
Pub Date : 2021-01-01 DOI: 10.16966/2473-1846.162
Tewari Dn, Chakrabarti Ak, Dutta S
Emergence of SARS-CoV-2 and associated COVID-19 pandemic is a major global healthcare problem because there is no specific drug to combat the disease. Number of infection is piling up day by day in exponential rate creating new record every week. Entire world is looking for urgent remedy but till now there is no specific treatment available for COVID-19 patients. In this critical situation, although vaccination is in its way, drug repurposing is very important which may be useful to overcome the unprecedented situation of COVID-19 pandemic. Cholesterol lowering drugs like statin therapy may be an additional support to combat the disease. Hexamethylene amiloride which has shown its effect in blocking E protein ion channels of coronaviruses leading to inhibition of viral replication may be considered for investigative trial.
SARS-CoV-2和相关的COVID-19大流行的出现是一个重大的全球卫生保健问题,因为没有特定的药物来对抗这种疾病。感染人数正以指数速度与日俱增,每周都在创造新的记录。全世界都在寻找紧急补救措施,但到目前为止,还没有针对COVID-19患者的具体治疗方法。在这种危急情况下,尽管疫苗接种受到阻碍,但药物重新利用非常重要,这可能有助于克服COVID-19大流行这一前所未有的局面。像他汀类药物这样的降胆固醇药物可能是对抗这种疾病的额外支持。六亚甲基氨酰已显示出阻断冠状病毒E蛋白离子通道,抑制病毒复制的作用,可考虑进行研究性试验。
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引用次数: 0
Compassionate Use of Opaganib For Patients with Severe COVID-19 奥帕加尼对重症新冠肺炎患者的同情使用
Pub Date : 2020-06-23 DOI: 10.1101/2020.06.20.20099010
R. Kurd, E. Ben-Chetrit, Hani Karameh, M. Bar-Meir
Background. Opaganib is a selective sphingosine-kinase (SK)-2 inhibitor with anti-inflammatory and anti-viral properties. Methods. We provided opaganib on a compassionate-use basis to patients with severe COVID-19. Patients who required oxygen support via high-flow nasal cannula (HFNC) were offered the treatment. For comparison, we used a control group with same-sex, same-severity patients. Results. Seven patients received at least one dose of opaganib since April 2, 2020. One patient, who received both hydroxychloroquine and azithromycin, developed diarrhea and all his medications were stopped. This was the only adverse effect possibly related to opaganib. A second patient was weaned of oxygen and discharged after receiving two doses of opaganib. Therefore, five patients were included in this analysis. Baseline characteristics were not significantly different between cases and controls. Patients treated with opaganib had significantly faster increase in lymphocyte count. All other clinical outcomes had a non-statistically significant trend in favor of the treatment group: median time to weaning from HFNC was 10 and 15 days in cases vs. controls (HR= 0.3, 95% CI: 0.07-1.7, p=0.2) ,time to ambient air was 13 vs.14.5 days (HR=0.4, 95% CI: 0.15-1.5), none of the cases required mechanical ventilation compared with 33% of controls. Conclusion. In this small cohort of severe COVID-19 patients, opaganib was safe and well tolerated with improvement in both clinical and laboratory parameters in all treated patients. The efficacy of opaganib for COVID-19 infection should be further tested in randomized placebo-controlled trials.
背景Opaganib是一种选择性鞘氨醇激酶(SK)-2抑制剂,具有抗炎和抗病毒特性。方法。我们在同情的基础上为重症新冠肺炎患者提供了奥帕加尼。通过高流量鼻插管(HFNC)需要氧气支持的患者接受了治疗。为了进行比较,我们使用了一个同性、同等严重程度患者的对照组。后果自2020年4月2日以来,7名患者至少接受了一剂奥帕加尼。一名同时服用羟氯喹和阿奇霉素的患者出现腹泻,所有药物都被停用。这是唯一可能与奥帕加尼有关的不良反应。第二名患者在接受两剂奥帕加尼后停止吸氧并出院。因此,本次分析包括5名患者。病例和对照组的基线特征没有显著差异。接受有机磷治疗的患者淋巴细胞计数增加速度明显加快。所有其他临床结果都有利于治疗组的无统计学意义的趋势:与对照组相比,病例从HFNC断奶的中位时间分别为10天和15天(HR=0.3,95%CI:0.07-1.7,p=0.02),与环境空气接触的时间分别为13天和14.5天(HR=0.04,95%CI:0.15-1.5),与33%的对照组相比没有病例需要机械通气。结论在这一小型新冠肺炎重症患者队列中,奥帕加尼安全且耐受性良好,所有接受治疗的患者的临床和实验室参数都有所改善。奥帕加尼治疗新冠肺炎感染的疗效应在随机安慰剂对照试验中进一步测试。
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引用次数: 9
Clinical Features and Follow-Up of SARS-Cov-2 Asymptomatic Carriers SARS-Cov-2无症状感染者临床特征及随访分析
Pub Date : 2020-01-01 DOI: 10.16966/2473-1846.156
Liu L, Yuan Mj, Hong Xq, Yu Y, S. X, Huang Y, Wang X, Li S, Li X, Shi Y
In the current global coronavirus disease (COVID-19) pandemic, asymptomatic transmission of the causative agent, severe acute respiratory coronavirus-2 (SARS-CoV-2), poses a considerable challenge for disease control. Furthermore, information on the clinical characteristics of asymptomatic carriers is limited. Here, we aimed to clarify the clinical features and obtain follow-up data of asymptomatic carriers to assist in the clinical management of carriers. This retrospective study included all asymptomatic SARS-CoV-2 carriers diagnosed at the First People’s Hospital of Yueyang (Hunan, China) and Hunan Provincial People’s Hospital (Changsha, China) between January 22 and March 26, 2020. Data including the epidemiology, clinical characteristics, laboratory test results, and chest computed tomography status were collected, with a follow-up of these cases. A total of 24 asymptomatic carriers were enrolled at the First People’s Hospital of Yueyang and Hunan Provincial People’s Hospital between 22 January 2020 and 26 March 2020. All patients had previously been exposed to SARS-CoV-2. Over the monitored time, patients experienced no symptoms and most laboratory findings were normal. The median time from contact to diagnosis was 9.6 days (range: 1-38 days), while that from diagnosis to discharge was 14.4 days (range: 6-24 days). Following discharge, all patients remained asymptomatic. However, five patients (20.83%) were re-admitted because a polymerase chain reaction (PCR)-based re-test of their specimens (4 throat swabs and 1 feces) showed that they were positive for SARS-CoV-2. The time to re-testing positively varied from 23 to 53 days post-diagnosis. The time to re-testing negative for SARS-CoV-2 by real-time reverse transcription PCR after re-testing positive was 3 to 11 days. In conclusion, although asymptomatic carriers have favorable outcomes, they should be closely monitored. Also, clear guidelines need to be formulated and close surveillance is required for the management of asymptomatic carriers.
在当前全球冠状病毒病(COVID-19)大流行中,病原体-严重急性呼吸道冠状病毒-2 (SARS-CoV-2)的无症状传播给疾病控制带来了巨大挑战。此外,关于无症状携带者的临床特征的信息有限。本研究旨在明确无症状携带者的临床特征并获得随访资料,以辅助临床对携带者的管理。本回顾性研究纳入了2020年1月22日至3月26日在中国湖南省岳阳市第一人民医院和湖南省人民医院诊断的所有无症状SARS-CoV-2携带者。收集流行病学、临床特征、实验室检查结果和胸部计算机断层扫描状况等资料,并对这些病例进行随访。2020年1月22日至3月26日,岳阳市第一人民医院和湖南省人民医院共登记无症状感染者24例。所有患者以前都接触过SARS-CoV-2。在监测期间,患者没有出现任何症状,大多数实验室检查结果正常。从接触到诊断的中位时间为9.6天(范围:1 ~ 38天),从诊断到出院的中位时间为14.4天(范围:6 ~ 24天)。出院后,所有患者均无症状。然而,5名患者(20.83%)再次入院,因为基于聚合酶链反应(PCR)的标本(4份咽拭子和1份粪便)重新检测显示他们对SARS-CoV-2呈阳性。再次检测呈阳性的时间从诊断后23天到53天不等。重新检测阳性后,通过实时反转录PCR重新检测为阴性的时间为3 ~ 11天。总之,尽管无症状感染者预后良好,但仍应密切监测。同时,要制定明确的指导方针,加强对无症状感染者的密切监测。
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引用次数: 0
Enrichment of Retroviral Sequences in Brain Tissue from Patients with Severe Demyelinating Diseases. 严重脱髓鞘疾病患者脑组织中逆转录病毒序列的富集。
Pub Date : 2017-08-01 Epub Date: 2017-07-16 DOI: 10.16966/2473-1846.132
J D Kriesel, P J Bhetariya, B K Chan, T Wilson, K F Fischer

Background: Our group has used deep sequencing to identify viral RNA signatures in human brain specimens. We have previously used this method to detect HSV1, GBV-C, and measles virus sequence in brain tissue from deceased donors. Deep sequencing was performed on brain specimens from a cohort of patients who died with progressive forms of MS, revealing evidence of increased expression of some human endogenous retrovirus (HERV) domains.

Objectives: Identify RNA sequences and new antigens involved in the pathogenesis of MS.

Methods: Deep sequencing was performed on RNA extracted from 12 progressive MS, 2 neuromyelitis optica (MS/NMO = demyelination group), 14 normal control, and 7 other neurologic disease (OND) control frozen brain specimens. The resulting single-ended 50 bp sequences (reads) were compared to a non redundant viral database representing (NRVDB) all 1.2 M viral records in GenBank. A retroviral gene catalog (RVGC) was prepared by identifying human genetic loci (GRCh37.p13) homologous to domains contained in the Gypsy 2.0 retro element database. Reads were aligned to the RVGC and human transcriptome with Bowtie2. The resulting viral hit rates (VHRs) were normalized by the number of high quality reads. The expression of human genes, including HERVs, was determined using Cufflinks. Comparisons between the groups were performed using the false discovery rate.

Results: Fifty to 131 million high quality reads per specimen were obtained. Comparison of the reads to the NRVDB suggested that the demyelination and OND specimens had higher VHRs against some retroviral sequences compared with the controls. This was confirmed by retroviral domain averaging. Gene expression analysis showed differential expression among some HERV sequences. Single read mapping revealed one envelope and one reverse transcriptase sequence record that were significantly enriched among the demyelination samples compared to the normal controls. Less restrictive (comprehensive) read mapping showed that 2 integrase, 2 core, 2 envelope, and 3 KRAB sequences that were overexpressed in the demyelination group.

Conclusions: These data demonstrate that some endogenous retroviral sequences are significantly overexpressed in these demyelination brain tissue specimens, but the magnitude of this overexpression is small. This is consistent with the concept of HERV activation as a part of the innate immune response.

背景:我们的研究小组已经使用深度测序技术来鉴定人类大脑标本中的病毒RNA特征。我们以前曾使用这种方法检测已故供者脑组织中的HSV1、GBV-C和麻疹病毒序列。对一组死于进展型多发性硬化症的患者的脑标本进行了深度测序,揭示了一些人类内源性逆转录病毒(HERV)结构域表达增加的证据。方法:对12例进展性多发性硬化症、2例视神经脊髓炎(MS/NMO =脱髓鞘组)、14例正常对照和7例其他神经系统疾病(OND)对照冷冻脑标本中提取的RNA进行深度测序。将得到的单端50 bp序列(reads)与GenBank中包含所有1.2 M病毒记录的非冗余病毒数据库(NRVDB)进行比较。通过鉴定与Gypsy 2.0 retro element数据库中结构域同源的人类遗传位点(GRCh37.p13),建立了逆转录病毒基因目录(RVGC)。用Bowtie2将Reads与RVGC和人类转录组进行比对。由此产生的病毒命中率(vhr)通过高质量读取的数量归一化。人类基因的表达,包括herv,是用袖扣来测定的。使用错误发现率进行组间比较。结果:每个标本获得了5000 - 1.31亿个高质量读数。与NRVDB的比较表明,脱髓鞘和OND标本对某些逆转录病毒序列的vhr比对照组高。逆转录病毒结构域平均证实了这一点。基因表达分析显示部分HERV序列之间存在差异表达。单读图谱显示脱髓鞘样品中的一个包膜和一个逆转录酶序列记录与正常对照相比显著丰富。限制性较低(综合)的读取图谱显示,脱髓鞘组中有2个整合酶、2个核心、2个包膜和3个KRAB序列过表达。结论:这些数据表明,一些内源性逆转录病毒序列在这些脱髓鞘脑组织标本中显着过表达,但这种过表达的幅度很小。这与HERV活化作为先天免疫反应的一部分的概念是一致的。
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引用次数: 7
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Journal of emerging diseases and virology
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