Mycoplasma-like Organisms Associated with Proliferation and Big Bud of Solanum lycocarpum St. Hil.

Mycoplasma-like organisms (MLOs) were found in sieve tubes of Solanum lycocarpum affected with prolferation and big bud. The MLOs were graft-transmitted to tomato plants which developed similar symptoms. The association of MLOs with affected but not with symptomless S. lycocarpum and tomato suggests that the abnormality is induced by MLOs. The possible role of S. lycocarpum as a reservoir of a strain of the tomato big bud is discussed.     

Mycoplasma-like Organisms in Phloem Elements of Ammobium alatum

Using transmission electron and fluorescent microscopes, Mycoplasma-like organisms (MLOs) were found in phloem cells of stems and leaves of Ammobium alatum. The diameter of these organisms ranged from 0.12–0.73 μm and averaged 0.4 μm. Symptoms induced by MLOs included chlorosis and reddening of leaves and winged stems, plant stunting and flower phyllody. This is the first report of MLOs associated with disease symptoms in A. alatum.     

Maintenance of MLOs (Mycoplasma-like Organisms) on Populus alba Micropropagation

Populus alba plantlet micropropagation has been used for maintaining MLOs more than three years in samples collected from infected trees in Paris. Symptoms were observed on plantlets obtained from subcultures of the apical, middle and basal parts of the stems, and from the roots. Fluorescent microscopy failed to detect MLOs in the apical part of the plantlets and showed that they increased near the roots. Electron microscopy confirmed their presence. Some root sieve tubes were completely packed with MLOs. The sensitivity of the two methods used, subculturing and microscopy, for detection of MLOs is discussed. The symptoms remained for one year in plants regenerated from diseased plantlets and grown in the greenhouse. Then they started to disappear.     

PCR detection of MLOs in quick decline-affected pear trees in Italy

Polymerase chain reaction (PCR) amplification, using primers derived from the 16S rRNA gene, followed by restriction fragment length polymorphism (RFLP) analysis with Alu I restriction endonuclease was used to detect myc-oplasma-like organisms (MLOs) associated with pear decline. MLOs were consistently detected in pear trees that suddenly wilted and died within a few days during summer, as well as in pears of the same orchards with symptoms similar to the slow form of pear decline. In both cases the same RFLP pattern was obtained. Declining pear trees were 5 to 8-yr-old cvs Williams, Kaiser and Max Red Bartlett grafted on to Pyrus communis seedling rootstocks. All the orchards affected by quick decline had severe attacks of pear psyllid (Cacopsylla pyri) during the year this study was performed and during the previous year. The results showed the suitability of DNA amplification by the polymerase chain reaction for the detection of pear decline MLOs and established that MLOs can be detected in infected tissues of dead trees.     

Susceptibility of Grafted Malus Taxa and Hybrids to Apple Proliferation Disease

Seedlings of a great number of Malus species, subspecies, cultivars and hybrids were graft-inoculated with the apple proliferation MLO. The scion cultivars were M. pumila cv.‘Cox's Orange Pippin’and‘Golden Delicious’. The grafted trees responded very differently to infection. According to recovery rate, witches’broom formation, mortality, and development of the MLO population, the tested material could be divided into 5 groups. Group I corresponds to the domestic apple M. pumila and is characterized by a low recovery rate, a low mortality, a high frequency of witches’broom formation, and a high MLO titer. Group II differs from group I mainly by a higher mortality. In group III, mortality is like in group II but recovery is higher while witches’broom formation and MLO titer are significantly lower. Group IV is characterized by a mortality of more than 50 %. Both witches’broom formation and the numbers of MLOs in the phloem are usually low. In group V, most of the trees recovered or showed never symptoms while mortality was low. After inoculation the MLO population was low or appeared degenerate. During recovery the number of MLO-positive samples decrease so that by the end of the observation period the organisms could not longer be detected in most cases. Group V consists of apomictic rootstock selections deriving from crosses of M. sieboldii and M. sargentii with M. pumila. Due to the combination of low mortality with the apparent elimination of the MLOs within a few years this group fulfills the requirement of resistant rootstocks suitable for controlling apple proliferation.     

Studies of the mycoplasma-like organism (MLO) in spinach leaves affected by the aster yellows disease

Summary Mycoplasma-like organisms (MLO) were found in the phloem of spinach (Spinacia oleracea L.) leaves infected with the agent of aster yellows disease by means of the leafhopperMacrosteles fascifrons Stål. The MLOs occurred mainly in mature sieve elements but were recorded in occasional phloem parenchyma cells as well. The MLO showed the typical features of this organism. The majority were ovoid or spherical, some were irregular in form or elongated. The larger bodies were commonly accompanied by small bodies which appeared to originate from the larger by budding. Profiles suggesting binary fission and filamentous forms containing ovoid condensations of cytoplasm were present. The bounding membrane showed the typical trilaminate structure, and DNA-like fibrils were discernible in those MLOs that had an electron lucent central region. In the denser bodies the fibrils were obscured. The MLO ribosomes were distinctly smaller than those in the host cytoplasm. The MLOs were degenerating in phloem cells that were disorganizing and collapsing in response to the infection. Structures in host cells that may be confused with MLO are described.This work was supported by the National Science Foundation grant GB-35228 to K. E and by Hatch and California Statewide Critical Applied Research Funds to the Departmem of Cell Physiology, University of California, Berkeley, California. The authors thank ProfessorJulius H.Freitag for providing the original strains of the aster yellows agent.     

Amplification of plasmid DNA to detect plant pathogenic mycoplasmalike organisms

The polymerase chain reaction (PCR) was employed to develop a specific assay for plant pathogenic mycoplasmalike organisms (MLOs). A cloned fragment of a plasmid from a severe strain of western aster yellows (AY)-MLO was sequenced to identify oligonucleotide primers for PCR. Amplified DNA fragments of the predicted size were obtained from DNA extracted from plants and insects infected with pear decline MLO, beet leafhopper-transmitted virescence agent, elm yellows MLO and several AY-MLO strains. No amplification occurred from healthy leafhopper or plant DNA. The PCR-based assay was over 500 times more sensitive than a _tilized_tion-based assay which _tilized a cloned AY plasmid fragment as a probe. With the PCR-based assay, MLOs could be detected using DNA samples of leafhoppers that were only crushed and boiled in buffer. Amplification of the target DNA was confirmed by digestion of the PCR product with Mbo I which yielded predicted sized fragments for all MLO strains except Bradford AY and eastern AY. Sequencing the PCR product from elm yellows and eastern AY-MLOs revealed greater than 90% homology, and the failure to restrict the PCR product with Mbo I was due to a single base change in the restriction endonuclease site. The ability of the assay to detect a wide range of MLOs with minimal sample preparation and high sensitivity will be useful in epidemiological studies of MLO-caused diseases.     

Five novel species of the anamorphic genus Candida in the Cyberlindnera clade isolated from natural substrates in Taiwan

Twelve strains representing five novel yeast species were isolated from natural samples distributed in mountain areas in Taiwan during 2007 and 2009. Sequence analysis of the D1/D2 domain of the large subunit (LSU) rRNA gene revealed that these species are members of the Cyberlindnera clade. These five new species have a greater than 1% difference from their closest relatives in the sequences of the D1/D2 domain of the LSU rRNA gene and were well separated from their closest relatives in terms of physiological characteristics. Moreover, a sexual state could not be found in these five novel yeast species. Therefore, the scientific names of Candida maesa sp. nov. (type strain GJ8L01^T), Candida takata sp. nov. (type strain EN25S01^T), Candida taoyuanica sp. nov. (type strain GY15S07^T), Candida hungchunana sp. nov. (type strain NC3W71^T) and Candida stauntonica sp. nov. (type strain GY13L05^T) were proposed to accommodate these yeasts.     

甘蓝型油菜抗茎倒材料的筛选与候选基因挖掘

该研究采用茎秆抗折力指标评价了200份甘蓝型油菜种质资源抗茎倒伏能力,据此筛选出极端抗茎倒材料和不抗茎倒材料各1份,随后测定了2份材料成熟期茎秆的理化组分含量,并对2份极端抗茎倒差异材料蕾苔期、盛花期茎秆进行转录组测序分析,为甘蓝型油菜抗茎倒伏的遗传改良奠定基础。结果表明:(1)200份甘蓝型油菜种质资源的茎秆抗折力和茎粗均为正态分布,均属于数量遗传性状,并依据茎秆抗折力和农艺性状筛选出生育期相近,株型相似,茎秆粗度差异不显著,但茎秆抗折力差异显著的极端不抗茎倒材料GY172和抗茎倒材料GY199。(2)GY199的韧皮部比GY172更加致密,而GY172成熟期茎秆中的半纤维素、木质素、中性洗涤纤维及总可溶性糖含量均显著高于GY199,而其纤维素含量极显著低于GY199,即成熟期茎秆纤维素含量与这2个材料的茎秆抗折力呈正相关。(3)蕾苔期、盛花期茎秆转录组测序发现,碳代谢、碳固定、磷酸戊糖途径、氨基酸的生物合成、糖酵解/糖异生等途径的14个基因(BnaA10G0056100ZS、BnaC08G0455100ZS、BnaA08G0262400ZS、BnaC08G0239700ZS、BnaA07G0362300ZS、BnaC02G0081300ZS、BnaC04G0273000ZS等)以及纤维素合成相关的9个基因(BnaA05G0152200ZS、BnaA01G0411100ZS、BnaA03G0018900ZS、BnaA03G0037800ZS等)在抗茎倒材料GY199中显著上调表达,这些基因可能参与调控了茎秆强度性状,可作为油菜抗茎倒候选基因。     

Studies on population dynamics and spatial distribution of leafhoppers in vineyards (Homoptera: Cicadellidae)

Thirty-two species of Cicadellidae, including the Macropsinae, Agalliinae, Penthimiinae, Aphrodinae, Cicadellinae, Typhlocybinae and Deltocephalinae, 10 of which were already known as phytoplasma vectors, were captured in vineyards using yellow sticky traps. Adult population dynamics of the most abundant species of Penthimiinae and Deltocephalinae were studied over the whole growing season. Penthimia nigra was captured in May and June, Anoplotettix fuscovenosus in June-August, Fieberiella florii in August-October, Macrosteles sexnotatus in May and October, Scaphoideus titanus in July-September, Thamnotettix spp. (Th. confinis, Th. dilutior, Th. exemtus, Th. zelleri) in April-June, while Euscelidius variegatus, Neoaliturus fenestratus, Platymetopius major and Psammotettix spp. (P. alienus, P. confinis) were trapped throughout the growing season. The aggregation level of the above species was investigated by means of Taylor's power law. A. fuscovenosus showed a nearly random distribution in vineyards (0.95 < b < 1.11), while N. fenestratus, P. major and S. titanus were strongly aggregated (1.32 < b < 1.81). The other species showed intermediate levels of aggregation (1.12 > b < 1.32). The results indicate that at least six Deltocephalinae species, A. fuscovenosus, E. variegatus, F. florii, M. sexnotatus, N. fenestratus and S. titanus, known as phytoplasma vectors and commonly found in vineyards, could play a role in Grapevine Yellows (GY) epidemiology. GY transmission trials with these species are needed.     

Loss of the ssrA genome island led to partial debromination in the PBDE respiring Dehalococcoides mccartyi strain GY50

Polybrominated diphenyl ethers (PBDEs), chemicals commonly used as flame‐retardants in consumer products, are emerging persistent organic pollutants that are ubiquitous in the environment. In this study, we report a PBDE‐respiring isolate – Dehalococcoides mccartyi strain GY50, which debrominates the most toxic tetra‐ and penta‐BDE congeners (～1.4 µM) to diphenyl ether within 12 days with hydrogen as the electron donor. The complete genome sequence revealed 26 reductive dehalogenase homologous genes (rdhAs), among which three genes (pbrA1, pbrA2 and pbrA3) were highly expressed during PBDE debromination. After 10 transfers of GY50 with trichloroethene or 2,4,6‐trichlorophenol as the electron acceptor instead of PBDEs, the ssrA‐specific genome island (ssrA‐GI) containing pbrA1 and pbrA2 was deleted from the genome of strain GY50, leading to two variants (strain GY52 with trichloroethene, strain GY55 with 2,4,6‐trichlorophenol) with identically impaired debromination capabilities (debromination of penta‐/tetra‐BDEs ceased at di‐BDE 15). Through analysis of Illumina paired‐end sequencing data, we identified read pairs that probably came from variants that contain ssrA‐GI deletions, indicating their possible presence in the original strain GY50 culture. The two variant strains provide real‐time examples on rapid evolution of organohalide‐respiring organisms. As PBDE‐respiring organisms, GY50‐like strains may serve as key players in detoxifying PBDEs in contaminated environments.     

Nonradioactive Screening Method for Isolation of Disease-Specific Probes To Diagnose Plant Diseases Caused by Mycoplasmalike Organisms

DNA fragments of tomato big bud (BB) mycoplasmalike organism (MLO) in diseased periwinkle plants (Catharanthus roseus L.) were cloned to pSP6 plasmid vectors and amplified in Escherichia coli JM83. A nonradioactive method was developed and used to screen for MLO-specific recombinants. Cloned DNA probes were prepared by nick translation of the MLO recombinant plasmids by using biotinylated nucleotides. The probes all hybridized with nucleic acid from BB MLO-infected, but not healthy, plants. Results from dot hybridization analyses indicated that several MLOs, e.g., those of Italian tomato big bud, periwinkle little leaf, and clover phyllody, are closely related to BB MLO. The Maryland strain of aster yellows and maize bushy stunt MLOs are also related to BB MLO. Among the remaining MLOs used in this study, Vinca virescence and elm yellows MLOs may be very distantly related, if at all, to BB MLO. Potato witches' broom, clover proliferation, ash yellows, western X, and Canada X MLOs are distantly related to BB MLO. Southern hybridization analyses revealed that BB MLO contains extrachromosomal DNA that shares sequence homologies with extrachromosomal DNAs from aster yellows and periwinkle little leaf MLOs.     

Mycoplasma–like Organisms Associated with a Grapevine Yellows Disease Occurring in Italy

Transmission electron microscopy of tissues from Vitis vinifera L. plants, naturally infected with a yellows disease similar to flavescence dorée (FD), revealed the presence of pleomorphic mycoplasmalike organisms (MLOs). These occurred in varying concentrations in mature sieve tube elements of leaf veins. Generally the concentration was very low, although large populations of MLOs were found colonizing almost the entire lumen of two cells. The micro–organisms varied considerably in size, shape and electron opacity. Spherical, oval and filamentous forms were recognized. The bodies showed the typical ultrastructural details of other known plant pathogenic MLOs. They were bounded by a smooth trilaminar membrane and contained ribosome–likegranules and DNA–like strands.     

Effects and statistical optimization of fermentation conditions on growth and poly (vinyl alcohol)-degrading enzyme production of Streptomyces venezuelae GY1

The effects of environmental conditions, including temperature, pH and dissolved oxygen, on growth and production of polyvinyl alcohol (PVA)-degrading enzymes of the newly-isolated strain Streptomyces venezuelae GY1 were investigated. The medium composition for strain GY1 was studied first by single factorial design and then optimized using a central composite design. PVA with high saponification is better for growth of, and PVA-degrading enzyme production by S. venezuelae GY1 compared with PVA with low saponification, in contrast with the characteristics of other bacteria producing PVA-degrading enzymes. The optimal temperature and initial pH for production of PVA-degrading enzyme by strain GY1 was 30°C and 7.0, respectively. The optimal medium composition for PVA-degrading enzyme production is: 1.01 g L^?1 of PVA1799, 0.307 g L^?1 of NaNO₃ and 0.512 g L^?1 of MgSO₄?7H₂O.     

Studies on Taxonomic Relationships of Mycoplasma–like Organisms by Southern blot Analysis

Chromosomal DNA fragments from the mycoplasma-like organisms (MLOs) associated with American aster yellows, apple proliferation, clover phyllody, and vaccinium witches' broom were cloned. Several MLO-specific fragments from each of these four isolates and a sequence from the 16S rRNA gene of an aster yellows MLO were used in Southern blot hybridizations to investigate the taxonomic relationships of 26 pathologically and geographically diverse MLOs. These MLOs were divided into four categories according to the symptoms induced in periwinkle. Genotypically, these isolates represented four groups (16S RFLP groups) of a classification based on restriction fragment length polymorphisms (RFLP) and sequencing data of the 16S rRNA gene. Probes from three isolates of one symptom category hybridized with isolates from all symptom categories. This result indicates that classification of MLOs by symptomatology does often not coincide with genetic relationships. The hybridization results confirmed the findings, of the 16S RFLP classification that most MLOs from herbaceous plants, especially those inducing virescence in periwinkle, are interrelated. These isolates, which were assigned to one 16S RFLP group, could be further differentiated in this study. Itcould be shown that aster yellows, clover phyllody, stolbur, and safflower phyllody and sandal spike are caused by distinct MLOs. The MLOs associated with apple proliferation, vaccinium witches' broom, and witches' broom of lime as well as two isolatesfrom, stone fruits could also be recognized as distinct organisms.     

牛源金黄色葡萄球菌FnBPA-A分子不同遗传多态性重组质粒的免疫生物学特性的比较

【目的】为了解Fn BPA-A分子遗传多态性对新疆部分地区牛源金黄色葡萄球菌免疫生物学特性的影响。【方法】对采自新疆不同地区的牛源金黄色葡萄球菌Fn BPA-A氨基酸序列进行分析,构建了Fn BPA-A 8个不同遗传多态性的真核重组质粒,分别免疫C57BL/6小鼠,收集免疫后的抗血清。对不同重组质粒免疫小鼠后免疫保护力进行比较分析。【结果】进化树显示GS801、GS819、GS856属于同一分支,GW10-1、GW20-2、GY288、GY309为同一分支,GY278为一分支。免疫小鼠并进行攻击保护检测,GW20-2、GS801、GS819、GS856与GY288免疫组对小鼠的免疫保护率较高,GY278免疫组免疫保护率最低。【结论】Fn BPA-A分子的遗传多态性可以影响免疫小鼠的免疫水平和攻毒保护力。     

Use of Polyclonal Antibodies to Identify Mycoplasma-like organisms (MLOs) From the Sudan and from Thailand

Rabbit polyclonal antibodies prepared against faba bean phyllody MLO from the Sudan reacted with its homologous antigen and with extracts of Catharanthus roseus experimentally infected with the same or a related MLO from Crotalaria saltiana showing symptoms of phyllody disease, as well as with extracts of naturally MLO-infected C. saltiana growing in the field in the Sudan. The antibodies also reacted positively with extracts of C. roseus experimentally infected with Crotalaria juncea phyllody MLO and soybean phyllody MLO from Thailand. Polyclonal antibodies prepared against an MLO associated with witches' broom disease in C. juncea reacted positively in ELISA tests with homologous antigen extracts from naturally infected C. juncea as well as with extracts from experimentally infected C. roseus and with extracts prepared from Sesamum indicum plants with phyllody symptoms growing in Thailand. There was no reaction between these antibodies and extracts from C. roseus plants infected with the MLOs associated with C. juncea phyllody or with soybean phyllody. No cross reactions were observed among the antigens and antibodies of the two MLO groups by immunoflorescence, ELISA or western blotting. However, the molecular weight of the principal protein antigen, determined by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and western blotting was the same for both types of MLO. Serologically-similar MLOs thus occur in the Sudan and in Thailand, where they are associated with phyllody symptoms in C. saltiana and faba bean and with C. juncea and soybean, respectively. A second, serologically distinct MLO group was also found infecting C. juncea and S. indicum in Thailand but MLOs from this group have not yet been identified in crops from the Sudan.     

ELISA and dot-blot detection of flavescence dorée-MLO in individual leafhopper vectors during latency and inoculative state

Flavescence dorée, an MLO (mycoplasma-like organism) disease of grapevine, is vectored in the field by the leafhopperScaphoïdeus littoralis, and in the laboratory fromVicia faba toVicia faba by the leafhopperEuscelidius variegatus. Antibodies to partially purified MLOs from broadbeans orE. variegatus were raised in rabbits. ELISA allowed individual assay of leafhoppers almost without background to healthy leafhopper control. Positive ELISA reading was associated with biological transmission and demonstrated the infection in noninoculative leafhoppers, even during latency. Thus, ELISA detection was fast and more accurate than inoculative state. A first multiplication of antigen, leading to infectivity of leafhoppers, was followed by a fast and strong multiplication during the following weeks. Males were particularly affected. Differential acquisition between individuals was shown. Application toS. titanus naturally contaminated in the field allows survey of epidemic outbreak and search for other vector species.     

Differential plant growth and osmotic effects of two maize (<Emphasis Type="Italic">Zea mays</Emphasis> L<Emphasis Type="Italic">.</Emphasis>) cultivars to exogenous glycinebetaine application under drought stress

We investigated the effects of exogenous glycinebetaine (GB) and drought stress (DS) on grain yield (GY) and production of dry matter (DM) and osmolytes in two maize (Zea mays L.) cultivars i.e. Shaandan 9 (S₉) and Shaandan 911 (S₉₁₁) during the entire growing period. Drought stress substantially reduced DM and GY but increased free proline, endogenous GB, soluble sugar and K⁺ concentrations in leaves of both cultivars. The DM production, GY, drought index (DI) and concentrations of these osmolytes were greater for S₉ than those for S₉₁₁ under DS. The significant differences in these parameters suggested that S₉ was more drought-tolerant as compared to S₉₁₁. Additionally, foliar application of GB increased the concentrations of all osmolytes measured, DM and GY of both cultivars under DS. These positive responses of exogenous GB spray were more pronounced in S₉₁₁ as compared to those in S₉. Further correlation analysis involving a number of parameters indicated that maize production was tighterly correlated with accumulation of the osmolytes measured during DS rather than well-watered controls. Accordingly, this study demonstrated the notion of an anti-drought role of exogenous GB by osmoregulation under DS, particularly in this drought sensitive cultivar. Thus, exogenous GB application might be firstly used with drought sensitive species/cultivars when exposed to DS.