蓝莓拟茎点枝枯病的病原

近期在山东省蓝莓种植区发现一种枝枯病害。为明确其致病菌,通过单孢分离方法和接种试验获得3个菌株。通过形态学特征观察和rDNA-ITS序列分析,确定该病原菌为乌饭树拟茎点霉Phomopsis vaccinii,即越橘间座壳Diaporthe vaccinii的无性阶段。这是乌饭树拟茎点霉所致蓝莓枝枯病在国内的首次发现。     

四川主要松树内生拟盘多毛孢

从5种松树健康的枝、叶、干中共分离了2,400个组织块,得到199株内生拟盘多毛孢Pestalotiopsis,形态学和分子生物学鉴定分属于11个种,平均分离率为8.29%。所得11种内生拟盘多毛孢都是首次在四川的松属植物中分离得到,其中葡萄生拟盘多毛孢P.uvicola和山桃草拟盘多毛孢P.gaurae为首次在松树上分离得到。基于ITS序列的分子系统发育分析显示松树内生拟盘多毛孢种类之间存在一定的遗传差异,部分内生拟盘多毛孢与病原拟盘多毛孢的ITS序列具有很高的同源性。     

山茶灰斑病病原菌斑污拟盘多毛孢的研究

山茶灰斑病病原菌的正名为斑污拟盘多毛孢Pestalotiopsis maculans(Cda.)Nag Raj,山茶盘多毛孢Pestalotia guepini Desm.和山茶拟盘多毛孢Pestalotiopsis guepini(Desm.)Stey.均为其异名。本文根据作者对自1978年以来采集的大量标本和分离菌株的研究,记述了斑污拟盘多毛孢的形态学、培养性状、致病性及寄主范围、电泳图谱等特征,并附有讨论。     

草莓拟盘多毛孢叶斑病的病原菌

于2013年在北京市房山区发现了一种新的草莓叶部病害,为明确引起该病害的病原菌种类,采用组织分离法对病叶进行了病原菌的分离,经纯化得到一株病原菌CMF4。通过室内人工接种对该菌株的致病性和寄主范围进行测定,发现该菌株可以导致草莓叶片坏死和果实腐烂,可引起有伤供试植物牡丹、海棠、芍药、杏、樱桃、桃和月季发病,但不能无伤侵入,对人工接种发病的植株进行病原菌再分离可得到原接种病原菌。采用rDNA-ITS序列分析方法并结合该病原菌的形态特征进行鉴定,发现引起该病害的病原菌为棒孢拟盘多毛孢Pestalotiopsis clavispora。这是棒孢拟盘多毛孢所致草莓叶斑病在国内的首次报道。     

中国海南内生拟盘多毛孢

2004 至 2005 年期间,从我国海南地区 95 种植物中分离鉴定了 43 种内生拟盘多毛孢,包括 5 个新组合,16 个内生拟盘多毛孢新记录种。5 个原归在盘多毛孢属 Pestalotia 的种重组到拟盘多毛孢属Pestalotiopsis 中,它们是二色拟盘多毛孢 P. bicolor,金鸡纳树拟盘多毛孢 P. cinchonae,密花拟盘多毛孢P. lambertiae,草原拟盘多毛孢 P. pampeana 和露兜树拟盘多毛孢 P. pandani。对 5 个新组合进行了重新描述和图解,其它 16 个内生拟盘多毛孢新记录种列出名录。     

拟盘多毛孢属真菌的新种*

报导拟盘多毛孢属真菌的8个新种。这8个新种是:近似状拟盘多毛孢Pestalotiopsis affinis、山姜拟盘多毛孢P. alpiniae、见血封喉拟盘多毛孢P. antiaris、五桠果拟盘多毛孢P. dilleniae、广西拟盘多毛孢P. kuwangsiensis、莲拟盘多毛孢P. nelumbinis、木荷拟盘多毛孢P. schimae、和神秘果拟盘多毛孢P. synsepali。新种的模式标本保存在广西大学植保系标本室。     

植物内生拟盘多毛孢的生物多样性

内生拟盘多毛孢是植物 (尤其是木本植物 )内生真菌的重要类群。分离自红豆杉的内生小孢拟盘多毛孢(Pestalotiopsismicrospora)能产生抗癌的代谢产物紫杉醇 ,因而引起了人们对内生拟盘多毛孢研究的兴趣。拟盘多毛孢内生于植物的根、茎、叶及繁殖体中 ,已鉴定的内生拟盘多毛孢有 2 3种。在已调查的植物中 ,内生拟盘多毛孢的定殖率有很大差异 ,在红树 (Rhizophoraapiculata)、椰子 (Cocosnucifer)、西藏红豆杉 (Taxuswallichiana)、茶梅 (Camelliasasanqua)、Fragraeabodenii和Cordemoyaintegrifolia等木本植物中 ,拟盘多毛孢是内生真菌的优势类群。一种拟盘多毛孢可内生于多种植物体内 ,一种植物也可有多种拟盘多毛孢内生 ,其分布与植物所处的生态环境和地域有关。在一定的宿主植物生理条件或外界环境条件下 ,某些内生拟盘多毛孢可转变为寄生或腐生。对植物内生拟盘多毛孢代谢产物的研究表明 ,拟盘多毛孢可产生多种次生代谢产物 ,包括抗癌物质 (紫杉醇和粗榧酸 )和抗菌物质 (环己烷类物质、粗榧酸和 pestaloside)。植物内生拟盘多毛孢的资源调查和开发应用具有广阔的前景。     

麻风树叶枯病菌的鉴定

作者于2009年在贵州麻风树栽培基地栽培的麻风树上发现一种叶部新病害,定名为麻风树叶枯病。该病主要危害植株叶片,叶片受害后初期产生椭圆形或不规则病斑,后期病斑连成片,常引起叶片过早脱落。从贵州罗甸麻风树栽培基地采集了16个叶枯病标样,经分离培养获得13个真菌分离物。通过致病性测定,证明菌株PE06为麻风树叶枯病的病原菌。通过形态学观察及其rDNA-ITS序列分析,将贵州麻风树叶枯病的病原菌鉴定为小孢拟盘多毛孢菌Pestalotiopsis microspora,这也是首次在麻风树叶片上发现由该病菌引起的病害。     

大熊猫体表一株海南拟盘多毛孢菌株

中国保护大熊猫研究中心雅安碧峰峡基地的一只大熊猫患皮肤病,从皮屑中分离到一株拟盘多毛孢菌GYMXP201108。进行了形态学观察和ITS序列分析,并构建系统进化树。结果表明,该菌株顶端附属丝短,1–3根,多数不具柄,与海南拟盘多毛孢Pestalotiopsis hainanensis模式菌株形态一致,ITS区序列分析也表明与海南拟盘多毛孢的序列相似性最高,为99.6%,因此鉴定为海南拟盘多毛孢,GenBank ID为KF551573。首次报道了海南拟盘多毛孢能在动物体表生存。     

中国南方内生拟盘多毛孢

采集并鉴定了我国南方8科17种植物的内生拟盘多毛孢23种,其中4个过去归在盘多毛孢属的种重组到拟盘多毛孢属中,它们是布氏拟盘多毛孢Pestalotiopsis briosiana,、芍药生拟盘多毛孢P.paeoniicola、亚角质拟盘多毛孢P.subcuticularis和窒息拟盘多毛孢P.suffocata,并对这4个新组合进行了重新描述和图解,其它19种列出名录。     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen derAlismataceae,Liliaceae, Juncaceae,Cyperaceae, Poaceae undAraceae

Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.

     

Identification and Characterization of the First Equine Parainfluenza Virus 5

正Dear Editor,Parainfluenza virus 5 (PIV5), known as canine parainfluenza virus in the veterinary field, is a negative-sense,nonsegmented, single-stranded RNA virus belonging to the Paramyxoviridae family (Chen 2018). The virus was first reported in primary monkey kidney cells in 1954 (Hsiung1972), then it has been frequently discovered in various     

Pathogenic Characterization and Full Length Genome Sequence of a Reassortant Infectious Bursal Disease Virus Newly Isolated in Pakistan

<正>Dear Editor,Infectious bursal disease (IBD) is one of the most important diseases of the poultry. The IBD virus (IBDV), a nonenveloped virus belonging to the Birnaviridae family with a genome consisting of two segments of double-stranded RNA (segments A and B), targets B lymphocytes of bursa of Fabricious leading to immunosuppression. In Pakistan,poultry farming is the second biggest industry and IBD is the second biggest disease threating the poultry sector.However, there is limited genome information of IBDV     

Mink Circovirus Can Infect Minks,Foxes and Raccoon Dogs

正Dear Editor,Mink circovirus (MiCV), which is clustered in the genus Circovirus of the family Circoviridae, was first described in minks from farms in Dalian, China in 2013 (Lian et al.2014). The complete single-stranded circular genome of the virus is 1,753 nucleotides long and contains two major open reading frames (ORFs), designated ORF1 (Rep gene)and ORF2 (Cap gene)(Lian et al. 2014; Ge et al. 2018).Sequence analysis has shown that MiCV is most closely     

CypA Regulates AIP4-Mediated M1 Ubiquitination of Influenza A Virus

Cyclophilin A (CypA) is a peptidyl-prolyl cis/trans isomerase that interacts with the matrix protein (M1) of influenza A virus (IAV) and restricts virus replication by regulating the ubiquitin–proteasome-mediated degradation of M1. However,the mechanism by which CypA regulates M1 ubiquitination remains unknown. In this study, we reported that E3 ubiquitin ligase AIP4 promoted K48-linked ubiquitination of M1 at K102 and K104, and accelerated ubiquitin–proteasome-mediated degradation of M1. The recombinant IAV with mutant M1 (K102 R/K104 R) could not be rescued, suggesting that the ubiquitination of M1 at K102/K104 was essential for IAV replication. Furthermore, CypA inhibited AIP4-mediated M1 ubiquitination by impairing the interaction between AIP4 and M1. More importantly, both the mutations of M1 (K102 R/K104 R) and CypA inhibited the nuclear export of M1, indicating that CypA regulates the cellular localization of M1 via inhibition of AIP4-mediated M1 ubiquitination at K102 and K104, which results in the reduced replication of IAV.Collectively, our findings reveal a novel ubiquitination-based mechanism by which CypA regulates the replication of IAV.