鸡油菌的25S rDNA部分序列及其系统学意义

菌物分类学家通常根据形态学,解剖学和显微观察特征的分析把鸡油菌类真菌置于非褶菌目Ａｐｈｙｌｌｏｐｈｏｒａｌｅｓ中或在非褶菌目和具正的伞菌之间,但由于缺乏足够的科学证据,有关其进化历史及其在担子菌中的系统发育位置等方面的关系等的各种假设,一直都存在着激烈的争论。本文从分子系统学角度出发,对鸡油菌Ｃａｎｔｈａｒｅｌｌｕｓ ｃｉｂａｒｉｕｓ的２５Ａ ｒＤＮＡ部分序列进行了测定,并与另外１０目的１３个担子     

鸡油菌属的研究概况与展望

鸡油菌属Cantharellus Adans. ex Fr. 在担子菌中是一个具有独立演化路线的类群, 隶属于担子菌门,同担子菌纲, 鸡油菌目, 鸡油菌科。该属全球分布广泛, 目前有65种, 中国曾记载9种。本文回顾了该属的研究历史, 结合自己的研究成果,着重对本属各分类单元的划分和命名, 相近种的区分, 鸡油菌C. cibarius Fr. 和管形鸡油菌C. tubaeformis Fr.: Fr. 复合群以及生态保护和仿生栽培等方面研究中存在的疑问和纷争进行了论述。最后,作者对我国鸡油菌属的生物多样性     

中国多孔菌名录

本文中的多孔菌系指广义非褶菌目中具有孔状子实层体的种类,按照现代分类系统包括担子菌门中多孔菌目、锈革孔菌目、褐褶菌目、糙孢孔目、革菌目、糙孢革菌目和红菇目中孔状子实体的种类,还有伞菌目、阿太菌目、鸡油菌目和木耳目中个别属,如网孔菌属、胶孔菌属、榆孔菌属、牛排菌属和纵隔孔菌属等的种类。基于作者采集的1万余号标本和国内主要标本馆标本的研究,对中国多孔菌的种类进行了系统总结,目前有604种多孔菌发现于中国,多孔菌数量位居世界第一。对中国多孔菌的名称按新近研究成果和最新命名法规(维也纳法规)进行了订正。对121种新拟了汉语学名。     

短裙竹荪和白鬼笔18SrDNA部分序列及其系统学意义

以短裙竹荪 [Dictyophoraduplicata(Bosc.)Fisch.]和白鬼笔 (PhallusimpudicusL.:Pers)作为鬼笔目 (Phal lales)的代表种 ,将其部分 1 8SrDNA序列与担子菌门 (Basidiomycota)其他科目 1 2个代表种已知的相关序列进行对比分析 ,以接合菌总状毛霉 (MucorracemosusFres.)为外类群构建系统树 ,探讨鬼笔目在系统分类学中的地位及其亲缘关系。结果表明 ,鬼笔目中竹荪属 (Dictyophora)与鬼笔属 (Phallus)的关系最为密切 ;其次它们与笼头菌科 (Clathraceae)的三叉鬼笔属 (Pseudocolus)关系较近 ,这与传统形态学分类系统一致。此外 ,鬼笔目与J櫣ｌｉｃｈ分类系统中的钉菇目 (Gomphales)、高腹菌目 (Gautieriales)、枝瑚菌目 (Ramariales)及鸡油菌目 (Cantharel lales)的关系较其他目更为密切 ,而与牛肝菌目 (Boletales)和腹菌类的马勃目 (Lycoperdales)及硬皮马勃目 (Scle rodermatales)的亲缘关系则相对较远。这一结果支持了Kirk等将钉菇目、高腹菌目和枝瑚菌目划为鬼笔目的分类观点。     

北京地区手参内生真菌的区系组成分析

手参Gymnadenia conopsea是一种地生兰科植物,也是中国传统中药材之一。研究以ITS1为目标序列,应用 Illumina MiSeq高通量测序技术对北京地区松山和百花山的手参内生真菌区系组成进行测定分析。结果表明,从手参的根中获得有效序列50 420条,209个可操作分类单元（OTUs）,分属于3门9纲28目54科,包括盘菌纲Pezizomycetes（3个OTU）、伞菌纲Agaricomycetes（21个OTU）、锤舌菌纲Leotiomycetes（18个OTU）、粪壳菌纲Sordariomycetes（51个OTU）、接合菌纲Zygomycetes（18个OTU）、银耳纲Tremellomycetes（19个OTU）、散囊菌纲Eurotiomycetes（22个OTU）、酵母纲Saccharomycetes（8个OTU）、座囊菌纲Dothideomycetes（14个OTU）。其中,百花山手参根中内生真菌优势类群是鸡油菌目Cantharellales（38.62%）和柔膜菌目Helotiales（24.64%）真菌;松山手参的优势内生菌类群是盘菌目Pezizales（66.19%）和鸡油菌目Cantharellales（29.75%）真菌。这些结果利于系统了解手参根部内生真菌区系组成以及优势内生真菌类群,为今后开展相关内生真菌在手参人工繁育中的应用奠定了基础。     

用识别四个GC对的限制酶研究高等担子菌线粒体DNA

本文报道了用识别四个GC对的限制性内切酶HaeⅢ、CofI、MsPI酶切高等担子菌伞菌目（Agaricales）、非褶菌目（Aphyllophorales）12个菌株的总DNA,在琼脂糖凝胶上显现线粒体DNA带谱的结果。通过对带型、累加分子量、酶切片段数和同源性的分析表明,不同种类高等担子菌的线粒体DNA变化较大．研究还显示,以多种识别四个GC对的限制酶分析高等担子菌的线粒体DNA及其它们的RFLP,比只用HaeⅢ更灵敏有效。     

香菇代料栽培研究概况及展望

香菇代料栽培研究概况及展望宋士良（上海市农业科学院食用菌研究所,上海２０１１０６）香菇是木材腐朽菌,属真菌门担子菌纲伞菌目口蘑科Ｌｅｎｔｉｎｕｓ属,学名为Ｌｅｎｔｉｎｕｓｅｄｏ－ｄｅｓ（Ｂｅｒｋ．）Ｓｉｎｇｅｒ．１９８３年英国伞菌分类学家佩格勒（Ｄ．...     

座囊菌目及相关类群属间关系的系统学初探

本研究对座囊菌纲部分类群的18S和28SnrDNA部分序列片段进行分析,探讨它们属间的系统学关系。邻接法和简约法分析结果显示,座囊菌纲供试类群为单起源,形成三个独立的分支并获得较强的支持率,分别代表座囊菌目、葡萄座腔菌目和格孢腔菌目。结果还显示,座囊菌纲中分类地位不确定的属Macrovalsaria与Botryosphaeria的关系相对接近,应该归于葡萄座腔菌目;历史上分类地位有疑问的Neopeckia和Dothidotthia两个属处于不同的目中,前者属于座囊菌目,后者为葡萄座腔菌目的成员;座囊菌目的Plowrightia属并非单系群,该属成员分别与Dothidea、Neopeckia和Sydowia三个属聚类在一起;现行的Botryosphaeria属也非单系群,其属的概念有待澄清。格孢腔菌目参试的7个属形成一个单系群,但属间的支持率非常低,表明它们应该在较高的分类等级上予以区分;序列分析的结果支持了基于形态学特征将Phragmogibbera纳入格孢腔菌目的分类观点。     

青藏高原食草动物粪栖真菌的多样性

分别利用真菌通用引物和厌氧真菌特异引物构建了西藏地区3种反刍动物和1种单胃动物共8份新鲜粪样的ITS克隆文库,以通过系统发育分析解析其中好氧真菌与厌氧真菌的多样性。通用引物ITS文库测得324条真菌序列,分别属于子囊菌门Ascomycota 3个目、担子菌门Basidiomycota 2个目、接合菌门Zygomycota的1个目和严格厌氧的新丽鞭毛菌门Neocallimastigomycota,共24个OTUs。其中,子囊菌门相对丰度最高,占80.6%;新丽鞭毛菌门相对丰度最低,仅占0.6%。大部分OTUs与已知真菌属、种关系较远。厌氧真菌特异引物文库测得661条序列,全部属于新丽鞭毛菌门,包括所有已知的厌氧霉属Anaeromyces、盲肠菌属Caecomyces、肠霉属Cyllamyces、新丽鞭毛属Neocallimastix、奥式霉属Orpinomyces、胃梨囊霉属Piromyces 6个属和3个未培养的属级类群(NG9、NG10、NG11),共29个OTUs。其中3个已知的单中心属存在于所有反刍动物样品中,并以Piromyces相对丰度最高(37.4%)。单胃动物马粪样中全部为NG9类群。NG9是本研究新发现的属级类群,研究中同时揭示有多个未培养种和潜在的新种。研究结果证明青藏高原反刍动物粪栖真菌多样性较高,并存在丰富的未培养种和潜在的新属及新种。     

中国种子植物内生真菌资源及菌植协同进化

综述了中国种子植物内生真菌资源研究概况,比较了裸子植物和被子植物内生真菌种类,它们都具有肉座菌目(Hypocreales),粪壳菌目(Sordariales),散囊菌目(Eurotiales),毛霉目(Mucorales)及不产孢类(Myceliasterilia)内生真菌。裸子植物内生真菌涉及52个属,既包括高等的子囊菌和担子菌,也包括低等的卵菌(Oomycetes)和接合菌(Zygomycetes)类。被子植物涉及60个属,主要为高等的子囊菌(Ascomycetes)和担子菌(Basidiomycetes),低等的卵菌和接合菌报道很少。双子叶植物涉及40个属,单子叶植物内生真菌涉及30个属,两类被子植物所报道的内生真菌只有11个属相同。裸子植物与双子叶植物内生真菌相似程度较高,都具有炭角菌目(Xylariales)、格孢腔菌目(Pleosporales)、柔膜菌目(Helotiales)和白粉菌目(Erysiphales),刺盘孢菌属(Colletotrichum)、拟茎点霉属(Phomopsis)、枝孢霉属(Cladosporium)、地霉属(Geotrichum)等内真菌,共20个属相同。各类种子植物具有自己独特的一些内生真菌。还对植物与其内生真菌的协同进化关系进行了分析。     

Molecular phylogeny of Zygomycota based on EF-1alpha and RPB1 sequences: limitations and utility of alternative markers to rDNA

Earlier molecular phylogenetic analyses based on nuclear small subunit ribosomal DNA (nSSU rDNA) suggest that the Zygomycota are polyphyletic within the Chytridiomycota. However, these analyses failed to resolve almost all interordinal relationships among basal fungi (Chytridiomycota and Zygomycota), due to lack of sufficient characters within the nSSU rDNA. To further elucidate the higher-level phylogeny of Zygomycota, we have sequenced partial RPB1 (DNA dependent RNA polymerase II largest subunit) and EF-1alpha (translation elongation factor 1 alpha) genes from 10 and 3 zygomycete fungi, respectively. Independent molecular phylogenetic analyses were performed based on each sequence by distance and maximum likelihood methods. Although deep phylogenetic relationships among basal fungi still remain poorly resolved using either gene, the RPB1-based phylogeny identified a novel monophyletic clade consisting of the Dimargaritales, Harpellales, and Kickxellales. This result suggests that regularly formed septa (cross walls that divide hyphae into segments) with a lenticular cavity are plesiomorphic for this clade, and indicates the importance of septal pore ultrastructure in zygomycete phylogeny. In addition, a peculiar mucoralean genus Mortierella, which was considered to be distantly related to the other Mucorales based on previous nSSU rDNA analyses, was resolved as the basal most divergence within the Mucorales, consistent with traditional phenotypic-based taxonomy. Although the taxa included in our analysis are restricted, the monophyly of each order suggested by nSSU rDNA phylogeny is supported by the present RPB1-based analysis. These results support the potential use of RPB1 as an alternative marker for fungal phylogenetic studies. Conversely, the overall fungal phylogeny based on EF-1alpha sequence is poorly resolved. A comparison of numbers of observed substitutions versus inferred substitutions within EF-1alpha indicates that this gene is much more saturated than RPB1. This result suggests that the EF-1alpha gene is unsuitable for resolving higher-level phylogenetic relationships within the Fungi.     

Detecting morphological convergence in true fungi, using 18S rRNA gene sequence data.

For the true fungi, phylogenetic relationships inferred from 18S ribosomal DNA sequence data agree with morphology when (1) the fungi exhibit diagnostic morphological characters, (2) the sequence-based phylogenetic groups are statistically supported, and (3) the ribosomal DNA evolves at roughly the same rate in the lineages being compared. 18S ribosomal RNA gene sequence data and biochemical data provide a congruent definition of true fungi. Sequence data support the traditional fungal subdivisions Ascomycotina and Basidiomycotina. In conflict with morphology, some zygomycetes group with chytrid water molds rather than with other terrestrial fungi, possibly owing to unequal rates of nucleotide substitutions among zygomycete lineages. Within the ascomycetes, the taxonomic consequence of simple or reduced morphology has been a proliferation of mutually incongruent classification systems. Sequence data provide plausible resolution of relationships for some cases where reduced morphology has created confusion. For example, phylogenetic trees from rDNA indicate that those morphologically simple ascomycetes classified as yeasts are polyphyletic and that forcible spore discharge was lost convergently from three lineages of ascomycetes producing flask-like fruiting bodies.     

Evolutionary relationships among basal fungi (Chytridiomycota and Zygomycota): Insights from molecular phylogenetics

Evolutionary relationships of the two basal fungal phyla Chytridiomycota and Zygomycota are reviewed in light of recent molecular phylogenetic investigation based on rDNA (nSSU, nLSU rDNA), entire mitochondrial genomes, and nuclear protein coding gene sequences (e.g., EF-1alpha, RPB1). Accumulated molecular evidence strongly suggests that the two basal fungal phyla are not monophyletic. For example, the chytridiomycete order Blastocladiales appears to be closely related to the zygomycete order Entomophthorales. Within the Zygomycota, a monophyletic clade, consisting of the Dimargaritales, Harpellales, and Kickxellales, which is characterized by a shared unique septal ultrastructure, was identified. Moreover, evidence for the exclusion of zygomycete orders Amoebidiales and Eccrinales from the Fungi, and their placement at the Animal-Fungi boundary has been clearly documented. Microsporidia, a group of amitochondriate organisms currently under intensive study, is not supported as derived within the Fungi, but a fungal affinity cannot be ruled out. Taking these molecular phylogenetic studies into account, we proposed a hypothetical evolutionary framework of basal fungi.     

Nucleotide sequence of the gyrA gene of Arcobacter species and characterization of human ciprofloxacin-resistant clinical isolates

The nucleotide sequence of the gyrA gene of Arcobacter butzleri, Arcobacter cryaerophilus, Arcobacter cibarius, and Arcobacter skirrowii was determined. The deduced GyrA proteins are closely related to those of Wolinella succinogenes and Helicobacter pullorum, whereas those of Campylobacter species showed less sequence identity. The phylogenetic analysis of GyrA sequences provides a result similar to 16S rRNA gene sequence phylogenetic analysis and allows the discrimination among A. butzleri species. In addition, a Thr-->Ile mutation at amino acid 85 in the quinolone resistance-determining region was associated with ciprofloxacin resistance for two A. butzleri and one A. cryaerophilus ciprofloxacin-resistant strains.     

Group I Introns from Zygomycota: Evolutionary Implications for the Fungal IC1 Intron Subgroup

The origins of fungal group I introns within nuclear small-subunit (nSSU) rDNA are enigmatic. This is partly because they have never been reported in basal fungal phyla (Zygomycota and Chytridiomycota), which are hypothesized to be ancestral to derived phyla (Ascomycota and Basidiomycota). Here we report group I introns from the nSSU rDNA of two zygomycete fungi, Zoophagus insidians (Zoopagales) and Coemansia mojavensis (Kickxellales). Secondary structure analyses predicted that both introns belong to the IC1 subgroup and that they are distantly related to each other, which is also suggested by different insertion sites. Molecular phylogenetic analyses indicated that the IC1 intron of Z. insidians is closely related to the IC1 intron inserted in the LSU rDNA of the basidiomycete fungus Clavicorona taxophila, which strongly suggests interphylum horizontal transfer. The IC1 intron of C. mojavensis has a low phylogenetic affinity to other fungal IC1 introns inserted into site 943 of nSSU rDNA (relative to E. coli 16S rDNA). It is noteworthy that this intron contains a putative ORF containing a His–Cys box motif in the antisense strand, a hallmark for nuclear-encoded homing endonucleases. Overall, molecular phylogenetic analyses do not support the placement of these two introns in basal fungal IC1 intron lineages. This result leads to the suggestion that fungal IC1 introns might have invaded or been transferred laterally after the divergence of the four major fungal phyla. Received: 8 February 2001 / Accepted: 1 November 2001     

蝗科高级阶元的分子系统发育(英文）

迄今,蝗科内各分类阶元之间的系统发生关系大部分是未知的。本文用来自中国24种蝗科昆虫的12SrDNA和16SrDNA2个基因的联合序列(共795bp)数据,以锥头蝗科的锥头蝗(Pyrgomorpha conica)为外群,重建了分子系统树。研究结果表明,在12SrDNA与16SrDNA组成的联合数据中,转换的替代速率明显比颠换的替代速率高得多,核酸的替代已经发生了饱和。分子系统树表明:斑翅蝗亚科是一单系群,该亚科是一个合法的亚科,但斑腿蝗亚科和蝗亚科都不是单系群;斑翅蝗亚科在蝗科内是一个相对原始的类群,而稻蝗亚科比斑翅蝗亚科相对进化,比蝗科的其他亚科的种类相对原始。     

rDNA units are highly polymorphic in Scutellospora castanea (Glomales,Zygomycetes)

The ribosomal DNA (rDNA) units in the glomalean zygomycete fungus Scutellospora castanea were analyzed. Dot-blot assays allowed an estimation of 75 copies per genome. After constructing a genomic library in a phage λEMBL3 vector, 13 rDNA clones were screened and explored. PCR experiments confirmed their nature and allowed homologous probes to be obtained. Restriction-fragment length polymorphism (RFLP) analysis and hybridizations with 18 s and 25 s probes allowed their grouping into nine families. The 18 s gene from these 13 clones was partially sequenced. The resulting 550 bases sequences were analyzed, and a phylogenetic tree was inferred. This revealed that two clones contain one highly divergent rDNA family (rUSc1) by comparison with other known 18 s sequences from the database. A phylogenetic tree was constructed with the entire 18 s sequences of rUSc1, rUSc3 and those of seven species representative of the glomalean fungi, Glomus, Entrophospora, Acaulospora, Scutellospora and Gigaspora. This tree confirmed that the rUSc1 sequence is the neighbor of 18 s sequences from Glomus (Glomineae), while rUSc3 remained in the group of the Gigaspora and Scutellospora (Gigasporineae). A specific primer, rUSc1-1, was generated from the ITS region of rUSc1, and used for PCR amplification from single spores, depicting the presence of rUSc1 in the genome of S. castanea at a lower frequency than other units.     

Phylogeny of Rhigonematomorpha based on the complete mitochondrial genome of Rhigonema thysanophora (Nematoda: Chromadorea)

We determined the complete mitochondrial genome sequence of Rhigonema thysanophora, the first representative of Rhigonematomorpha, and used this sequence along with 57 other nematode species for phylogenetic analyses. The R. thysanophora mtDNA is 15 015 bp and identical to all other chromadorean nematode mtDNAs published to date in that it contains 36 genes (lacking atp8) encoded in the same direction. Phylogenetic analyses of nucleotide and amino acid sequence data for the 12 protein‐coding genes recovered Rhigonematomorpha as the sister group to the heterakoid species, Ascaridia columbae (Ascaridomorpha). The organization of R. thysanophora mtDNA resembles the most common pattern for the Rhabditomorpha+Ascaridomorpha+Diplogasteromorpha clade in gene order, but with some substantial gene rearrangements. This similarity in gene order is in agreement with the sequence‐based analyses that indicate a close relationship between Rhigonematomorpha and Rhabditomorpha+Ascaridomorpha+Diplogasteromorpha. These results are consistent with certain analyses of nuclear SSU rDNA for R. thysanophora and some earlier classification systems that asserted phylogenetic affinity between Rhigonematomorpha and Ascaridomorpha, but inconsistent with morphology‐based phylogenetic hypotheses that suggested a close (taxonomic) relationship between rhigonematomorphs and oxyuridomorphs (pinworms). These observations must be tempered by noting that few rhigonematomorph species have been sequenced and included in phylogenetic analyses, and preliminary studies based on SSU rDNA suggest the group is not monophyletic. Additional mitochondrial genome sequences of rhigonematids are needed to characterize their phylogenetic relationships within Chromadorea, and to increase understanding of mitochondrial genome evolution.     

Relationships among Nicotiana species revealed by the 5S rDNA spacer sequence and fluorescence in situ hybridization

To investigate phylogenetic relationships in Nicotiana, the intergenic spacer sequences of 5S rDNA were analyzed in species with 2n=18, 20 or 24, and amphidiploid species with 2n=48. The chromosomal localization of the 5S rDNA was determined by fluorescence in situ hybridization (FISH). In species with 2n=24 and their descendants, a major 5S rDNA-specific PCR fragment of 400–650 bp was obtained. The amphidiploid species contained similar length of 5S rDNA units derived from putative diploid progenitors. Among the five clones from each representative PCR fragment, some nucleotide exchanges and length heterogeneity were observed. The latter was due to variation in the spacer region, such as differences in the length of poly A and/or poly T tracts as well as insertions/deletions. Interspecific comparisons of each 5S rDNA sequence demonstrated that the spacer sequence could be divided into three regions. Excluding gaps from the aligned spacer sequences of 5S rDNA, phylogenetic trees were constructed. Each phylogenetic tree showed an almost identical topology even if different algorithms were applied. The chromosomal locations of the 5S rDNA in each species correlated with the phylogenetic topology. The phylogenetic trees were generally in agreement with the current classification. Received: 15 January 2001 / Accepted: 15 February 2001