简介：AbstractSFTS virus (SFTSV) is a novel bunyavirus, which was discovered as the etiological agent of severe fever with thrombocytopenia syndrome (SFTS) in China in 2009, and was now prevalent in at least 25 provinces in China. SFTS was subsequently identified in South Korea and Japan in 2012. To explore the molecular evolution and genetic characteristics of this newly identified pathogen, we reported 72 whole genome sequences of SFTSV, and built a dataset of SFTSV genome sequences containing 292 L-segment, 302 M-segment and 502 S-segment. We clearly divided SFTSV into six genotypes, Genotype A-F. It was found that genotype F was the dominant epidemic genotype of Japan, South Korea, and Zhejiang province of China. The coalescent analysis supported that SFTSV originated in the early 18th century from Zhejiang province, and Genotype F was the most primitive one. Henan, Hubei, and Anhui provinces which are located in Dabie Mountain area were mainly epidemic of Genotype A, which emerged relatively late but distributed widely. A total of 37 recombination events were identified, making SFTSV with a high recombination frequency (L segment 5.1%, M segment 3.6%, S segment 0.8%) among negative-strand segmented RNA viruses. It was identified that 19 reassortant strains belonged to 12 reassortment forms of SFTSV genome containing 6 newly identified forms. The reassortment virus and recombination in tick were both found for the first time. We also found many of genotype-specific mutation sites, 7 of which could be considered as potential molecular marker for genotype classification. This study promoted a more comprehensive understanding of the phylogeny and origin, and the genetic diversity of SFTSV, and it could help the studies of other newly discovered tick-borne bunyavirus as reference data and research ideas.

简介：AbstractSevere fever with thrombocytopenia syndrome (SFTS), caused by a novel identified bunyavirus SFTS virus (SFTSV), was an emerging viral infectious disease that was firstly reported in China. There are no licensed vaccines and therapeutics against SFTSV currently. B-Propiolactone (BPL) inactivated whole virions of SFTSV strain AH12 were prepared as experimental vaccine in different antigen dose with or without Al(OH)3 adjuvant. The experimental SFTS vaccine was a satisfying immunogen, which could efficiently trigger the development of high levels of SFTSV NP-specific IgG antibodies and neutralizing antibodies against SFTSV Strain HB29 in BALB/c and C57/BL6 mice, and could induce SFTS virus-specific cellular immune responses to a certain extent. A single dose of vaccine was immunogenically insufficient in BALB/c mice; the second and third dose resulted in significant boost in antibody response. The use of Al(OH)3 adjuvant resulted in higher antibody titers. The mediate-dose of vaccine could induce as high and equivalent level of antibody titer as that of high-dose. The experimental SFTS vaccine in mediate-and high antigen dose with adjuvant resulted in solid protection of C57/BL6 mice against wild-type SFTSV challenge with markedly accelerated virus clearance from blood and spleen compared with controls. The experimental SFTS vaccine prepared in this study could efficiently elicit virus specific humoral and cellular immune responses in both BALB/c and C57/BL6 mice, and could protect C57/BL6 mice against SFTS virus challenge. These results supplied evidence that inactivated vaccine was a promising vaccine candidate for the prevention of SFTSV infection.

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简介：AbstractEbola virus (EBOV) is one of the most pathogenic viruses in humans which can cause a lethal hemorrhagic fever. Understanding the cellular entry mechanisms of EBOV can promote the development of new therapeutic strategies to control virus replication and spread. It has been known that EBOV virions bind to factors expressed at the host cell surface. Subsequently, the virions are internalized by a macropinocytosis-like process, followed by being trafficked through early and late endosomes. Recent researches indicate that the entry of EBOV into cells requires integrated and functional lipid rafts. Whilst lipid rafts have been hypothesized to play a role in virus entry, there is a current lack of supporting data. One major technical hurdle is the lack of effective approaches for observing viral entry. To provide evidence on the involvement of lipid rafts in the entry process of EBOV, we generated the fluorescently labeled Ebola virus like particles (VLPs), and utilized single-particle tracking (SPT) to visualize the entry of fluorescent Ebola VLPs in live cells and the interaction of Ebola VLPs with lipid rafts. In this study, we demonstrate the compartmentalization of Ebola VLPs in lipid rafts during entry process, and inform the essential function of lipid rafts for the entry of Ebola virus. As such, our study provides evidence to show that the raft integrity is critical for Ebola virus pathogenesis and that lipid rafts can serve as potential targets for the development of novel therapeutic strategies.

简介：Whitespotsyndromevirus(WSSV)isoneofthemajorshrimppathogenscausinglargeeconomiclossestoshrimpfarming.Inanattempttoidentifytheenvelopeproteinsinvolvedinthevirusinfection,purifiedWSSVvirionsweremixedwiththreeantiseraagainstWSSVenvelopeproteins(VP39,VP124andVP187),individually.Andthentheywereinjectedintramuscularlyintocrayfish(Procambarusclarkii)toconductinvivoneutralizationassays.TheresultsshowedthatforgroupsinjectedwithvirionsonlyandgroupsinjectedwiththemixtureofvirionsandantiserumagainstVP124,thecrayfishmortalitieswere100%and60%onthe8thdaypostinfection,individually.ThevirusinfectioncouldbedelayedorneutralizedbyantibodyagainsttheenvelopeproteinVP124.QuantitativePCRwasusedtofurtherinvestigatetheinfluenceofthreeantiseradescribedaboveonthevirusinfection.TheresultsshowedthattheantiserumagainstVP124couldrestrainthepropagationofWSSVincrayfish.AlloftheresultssuggestedthattheviralenvelopeproteinVP124playedaroleinWSSVinfection.

简介：摘要发热伴血小板减少综合征病毒(severe fever with thrombocytopenia syndrome virus，SFTSV)是一种蜱传的新型布尼亚病毒，在中国大别山地区被首次发现，临床上可以引起严重发热、血小板减少等症状，致死率可达10%~30%。目前，SFTSV的致病机理和感染机制尚不清楚，还没有针对该病毒的特效药物和疫苗。本文对SFTSV的入胞机制、膜融合、复制、装配和出芽过程进行了综述，总结了目前SFTSV相关的治疗性抗体和抗病毒药物的研究进展，以期为我国SFTSV的疫苗和抗病毒药物的研发提供参考。

简介：AbstractFoot-and-mouth disease virus (FMDV), swine vesicular disease virus (SVDV) and classical swine fever virus (CSFV) all cause important animal diseases. FMDV affects many different cloven-hoofed animals, whereas SVDV and CSFV are restricted to domestic and feral pigs together with wild boar. Europe is normally free of these diseases, but occasionally outbreaks happen, which can cause huge economic losses. Handling of these viruses, in particular FMDV and CSFV, is only allowed within high containment laboratories and stables. Periodically such facilities need to be decommissioned for repair or closing down, which is done by cleaning and chemical disinfection, followed by fumigation due to residual risk from virus on surfaces in inaccessible places. However, building materials in older laboratories or stables that have housed infected animals may not be well-suited for fumigation. Heat treatment is another way of inactivating viruses. In this study, we have determined the survival of infectivity in air-dried virus samples on glass and plastic surfaces incubated at room temperature or heated to 70 °C for 1, 2, 3, 5 and 7 days. Each of the tested viruses was inactivated to below the limit of detection after 24 h or 48 h of incubation at 70 °C; in contrast, some of these viruses were still infectious after 7 days of incubation at room temperature. This study provides important information that can be used in relation to decontamination of buildings and in risk-assessments.

简介：继去年9月的‘樱花’病毒之后前些日子又有一个叫“正版骗子”的病毒在网络上流传开采．和“樱花”病毒相同．该病毒也是拿反病毒厂商的杀毒软件开涮．不但会终止这几款杀毒软件．还会弹出具有迷惑性语言的对话框，给国内杀毒软件的正版用户开了一个大大的玩笑。

简介：在xenotropic之间的潜在的协会鼠科的白血球过多症自从2006，病毒相关的gammaretrovirus(XMRV)和前列腺癌症(PCa)被记录了。查明这个协会是否是原因的，为推进我们PCa的生物机制的理解是重要的。总结可得到的信息在上流行病学并且协会的实验室调查结果，我们进行了PubMed电子数据库的文学搜索(从2006年3月到2011年2月)那检验了在XMRV和PCa之间的协会识别相关出版研究。尽管几研究显示出在XMRV和PCa之间的积极协会，更最近的研究没支持这个结论。积极调查结果可能由于人的样品的污染。进一步的研究被需要澄清这个协会。

简介：Liverinjuryisacharacteristicfeatureofhumanimmunodeficiencyvirus(HIV)infection,whichisthesecondmostcommoncauseofmortalityinHIV-infectedpatients.NowitisrecognizedthatliverplaysakeyroleinHIVinfectionpathogenesis.Antiretroviraltherapy(ART),whichsuppressesHIVinfectioninpermissiveimmunecells,islesseffectiveinhepatocytes,therebymakingthesecellsasilentreservoirofHIVinfection.InadditiontodirecthepatotoxiceffectsofHIV,certainARTtreatmentmodalitiesprovidehepatotoxiceffects.TheexactmechanismsofHIV-triggeredchronichepatitisprogressionarenotelucidated,buttheliverisadverselyaffectedbyHIV-infectionandlivercellsareprominentlyinvolvedinHIV-elicitedinjury.Theseeffectsarepotentiatedbysecondhitslikealcohol.Here,wewillfocusontheincidenceofHIV,clinicalevidenceofHIVrelatedliverdamage,interactionsbetweenHIVandlivercellsandtheroleofalcoholandco-infectionwithhepatotropicvirusesinliverinflammationandfibrosisprogression.

简介：Witheffectivecontrolandpreventionmeasures,thenumberofHIVcarriersandAIDSpatientsinChinacouldbelimitedto1.5millionin2010,saidChenXianyi,aseniorofficialwiththeMinistryofHealth.Butwithoutsuchsteps,therecouldbemorethan10million,Chenwarned.Chenmadetheremar...

简介：<正>Manyvirusesestablishlife-longinfectionsintheirnaturalhostwithfewifanyclinicalmanifestations.Therelationshipbetweenvirusandhostisadynamicprocessinwhichthevirushasevolvedthemeanstocoexistbyreducingitsvisibility,whilethehostimmunesystemattemptstosuppressandeliminateinfectionwithoutdamagetoitself.Wearenowbeginningtounderstandthatvirusescanemployavarietyofstrategiestoevadehostimmuneresponses.TheseincludeescapefromTcellrecognition,resistanceto

简介：AbstractThis paper reviews the current epidemics of human immunodeficiency virus (HIV) infection in China, particularly the globally available prevention strategies developed and implemented. This review focuses on HIV prevention measures in general, such as education, testing, and counseling and in specific responses to transmission modes, such as blood safety, harm reduction for people who inject drugs, and condom promotion to reduce sexual transmission. We also assess newly developed prevention measures, such as prevention treatment, pre-exposure prophylaxis, post-exposure prophylaxis, male circumcision, and promising potential future preventions, including microbicides and vaccines. Based on this assessment, we provide recommendations for their implementation in China. We conclude that there is no magic bullet for HIV prevention, particularly sexual transmission of the disease, but only a combination of these prevention strategies can control the HIV epidemic.

简介：ThepurposeofthisstudywastoconstructaneukaryoticDNAvectorencodingamultipleepitopeantigen(MFC)ofhepatitisCvirus(HCV)andahepatitisBsurfaceantigen(HBsAg),andexploretheeffectofHBsAggeneontheimmunityofHCVmultiple-epitopeDNAconstructinvitroandinvivoinmice.AnHCVDNAvector(pVAX1-HBs-MFC)wasconstructedbyfusingHBsAggenetotheNterminalofanHCVmultiple-epitopeantigengene.ThepVAX1-HBs-MFCwastransfectedintoHEK293TcellsanditsexpressionwasmeasuredbyELISAandWesternblotting.BALB/cmicewereintramuscularlyimmunizedwiththepVAX1-HBs-MFC,andanELISAapproachwasappliedtodeterminethespecificantibodytitersandsubtypesinthemouseserum.Thecross-reactivityoftheantibodieswasalsocheckedwithtwosynthesizedHCVhypervariableregion1(HVR1)peptides.TheIFN-γproductionandcellproliferationofthemousespleencellswereevaluatedbyELISAandMTS(3-[4,5-dimethylthiazol-2-yl]-5-[3-carboxymethoxyphenyl]-2-[4-sulfophenyl]-2H-tetrazolium,innersalt)assays,respectively.TheexpressionofpVAX1-HBs-MFCwasdetectableinthetransfectedHEK293Tcells.TheserumantibodyresponsewaseffectivelyelicitedinBALB/cmiceinjectedwithpVAX1-HBs-MFC.ThehighesttiterofantibodyagainstHCV(MFC)was1:1280,andtheratioofIgG2a/IgG1was1.50±0.12atthefifthweekafterfirstimmunization.Moreover,thecollectedmouseserumantibodyhadtheabilitytocross-reactwiththetwosynthesizedHCVHVR1peptides.ThestimulationindexofthemousesplenocytestoMFCwas1.79±0.07,andtheIFN-γlevelwas287±6pg/mlatweek21afterfirstimmunization.ThehighesttiteroftheantibodyincontrolBALB/cmiceimmunizedwithpVAX1-MFCwas1:320,andtheratioofIgG2a/IgG1was1.33±0.11atweek5post-immunization.Furthermore,thestimulationindexofthemousesplenocytescellstoMFCwas1.52+0.06,andtheIFN-γlevelwas225±9.3pg/mlatweek21post-immunization.TheHBsAggenecanenhancetheeffectsofanHCVmultiple-epitope

简介：瞄准：把在病人之间的标准肝炎B(HBV)种痘的反应与长期的丙肝作比较病毒(HCV)感染和健康个人。方法：这是未来的盒子控制研究。有长期的HCV感染和40健康控制的38个病人的一个总数被包括。种痘被20大杯recombinantHBsAg的注射在瞬间0，1和6点执行进三角肌肌肉。Anti-HBs集中是在最后剂量以后决定了3瞬间并且在二个组之间比较了。反应模式是被描绘(1)高反应当anti-HBs抗体效价是>时100IU/L，(2)低反应当效价是10-100IU/L时并且(3)没有反应当效价是<时10IU/L。结果：在耐心的组，有10/38(26.3%)非应答者，8/38(21.1%)低应答者并且20/38(52.6%)高应答者。在控制组的相应价值是2/40(5.0%)，7/40(17.5%)和31/40(77.5%)分别地。反应模式在二个组之间是统计上不同的。在里面多变量分析，吸烟是重要confounder，当HCV感染与更低的抗体反应失去了它的重要关联时。结论：有长期的HCV感染的病人趋于与健康个人相比对HBV种痘微弱地作出回应，尽管这关联不是独立的根据多变量分析。

简介：摘要目的探究江苏省发热伴血小板减少综合征血清新型布尼亚病毒（severe fever with thrombocytopenia syndrome virus，SFTSV）中和抗体消长及影响因素，为免疫防控提供理论依据。方法采集江苏省发热伴血小板减少综合征既往病例的血清样本，采用空斑减少中和试验对其进行SFTSV中和抗体检测，阐明其消长规律，应用Spearman相关和广义相加模型分析其影响因素。结果本研究共纳入2011—2018年江苏省发热伴血小板减少综合征既往病例95例，其血清SFTSV中和抗体总阳性率为98.95%（94/95），总体几何平均滴度为1∶221。抗体水平随病后时间的延长总体呈逐年下降趋势（F=2.31，P=0.03），急性期高病毒载量者抗体水平较高（t=2.23，P=0.03）。抗体水平与急性期病毒载量呈正相关关系（rs=0.30，P<0.01），与病后时间呈负相关关系（rs=-0.25，P=0.03）。广义相加模型结果显示，急性期病毒载量CT值在0~125 000 copies/mL范围内对其影响尤为显著；抗体水平于病后7—20个月期间下降明显，21—40个月期间趋于平缓，41—96个月期间持续下降。结论2011—2018年江苏省发热伴血小板减少综合征既往病例血清SFTSV中和抗体普遍呈阳性，具有自我保护能力。抗体水平随时间逐渐降低，且与急性期病毒载量呈非线性正相关关系，可进行针对性免疫防护。

简介：Thepurposeofthisstudyistodistinguishrespiratorysyncytialvirus(RSV)infectionandimmunologybetweenimmunocompetentandimmunocompromisedmurineandtoexploreimmunemechanismofRSVinfection.AtvarioustimepointsafterRSVinfectionofBALB/cmiceandnudemice,pulmonaryviraltiterswereassayed,RSVantigenwastestedbydirectimmune-fluorescentassayandimmunohistochemistry.PulmonarymRNAexpressionsofTolllikereceptor(TLR)2andTLR4wereassayedbyRT-PCR.CD4+cellsandCD8+cellsinperipheralbloodwereexaminedbyflowcytometryandplasmatotalIgEwasassayedbyELISA.Leukocytesinbronchoalveolarlavagefluid(BALF)andpulmonaryhistologywereidentifiedtoreflectairwayinflammation.ItwasfoundthatRSVtitersofbothmicepeakedonthe3rddaypostinfectionwithamuchhigherlevelofviraltiterinnudemicethaninBALB/cmiceandalongerviraldurationinnudemice(over9dayspostinfection)thaninBALB/cmice(6dayspostinfection).RSVinfectioninducedhigherviralantigenexpressioninnudemice(0.267±0.045)thaninBALB/cmice(0.168±0.031).RSVinfectionenhancedpulmonaryTLR4expressionofBALB/cmice(51.96%±11.34%)andnudemice(48.96%±12.35%)comparedwitheachcontrol(34.04%±10.06%and32.37%±9.87%respectively).CD4+peripheralbloodcellsincreasedinRSVinfectedBALB/cmice(66.51%±2.09%)comparedwiththecontrolBALB/cmice(51.63%±5.90%),andCD4+cellsandCD8+cellsweredeficientinnudemice.RSVinfectionincreasedplasmatotalIgEinbothmice,andBALB/cmicehadalargeramountofIgEonthe7thdaypostinfection(9.02ng/ml±2.90ng/ml)andonthe14thdaypostinfection(12.76ng/ml±4.15ng/ml)thancorrespondingnudemice(3.72ng/ml±1.06ng/mland7.62ng/ml±3.08ng/mlrespectivelyonthe7thand14thdaypostinfection).RSVinfectednudemicehadmoresevereairwayinflammationthaninfectedBALB/cmice.ItisconcludedthatBALB/cmiceandnudemicepresentedsimilarRSVinfectiouscharacteristics.However,

简介：AbstractInfection of humans by Powassan virus (POWV) occurs rarely but is potentially life-threatening. First isolated in Ontario, Canada in 1958, the presence of POWV has been confirmed in three countries: Canada, the USA, and Russia. Although a limited number of human cases has been reported thus far, the infection rate has shown signs of increasing during the 21st century. Interestingly, POWV and a genetically close variant, deer tick virus (DTV), are the only member of the tick-borne flaviviruses known to be endemic in North America and maintain in respective tick-host cycles. In this review, we briefly summarize current knowledge involving the epidemiology and etiology, pathogenesis and immunity, molecular evolution, and protein functions of POWV, aiming to increase our understanding of the virus and unlock the potential to control this lethal pathogen. These data may also provide tools to minimize the future threat of other emerging and re-emerging viruses.

简介：动态系统被考虑的流行病毒传播人口的一个类。用功能的homotopic分析方法，第一，起始的近似功能被选择。然后，任意的顺序近似分析答案连续地被获得。最后，获得的近似分析答案的精确性被描述。为流行病毒传播人口的各种各样的物理参数的影响动态系统被讨论。