Inoculum Sources for the Spread of Leaf Scald Disease of Sugarcane Caused by Xanthomonas albilineans in Guadeloupe

Leaf scald of sugarcane, caused by Xanthomonas albilineans, is thought to be spread mainly in infected cuttings and transmitted on infested cutting implements. Several observations made in Guadeloupe indicated that other means of spreading also occur. The dispersal of the pathogen outside sugarcane was investigated with plants inoculated by an antibiotic-resistant marked strain of X. albilineans and with plants naturally infested with wild strains of the pathogen. The bacteria were isolated in water droplets (rain or dew) on the surface of sugarcane leaves at dawn. It was also detected on the surface of dry leaves during the day by leaf imprinting onto a selective culture medium. The bacteria were much more frequently isolated from the surface of symptomatic leaves than from symptomless ones. Aerial dispersal of X. albilineans was investigated by placing Petri dishes containing selective culture medium between sugarcane plants but without direct contact with the leaves. The pathogen was isolated in four out of 270 dishes which were randomly set 3–14 h in a diseased field. These results indicated that the pathogen exuded from the leaves and then was spread by aerial means (rain, insects, …) or by leaf contact. The bacteria were also found in roots and rhizospheric soil of infested sugarcane stools suggesting that X. albilineans could be transmitted by root to root contact or by the soil. Finally, isolations of the pathogen in sugarcane inflorescences were positive. So, fuzz transmission may also occur.     

Surface polysaccharides and quorum sensing are involved in the attachment and survival of Xanthomonas albilineans on sugarcane leaves

Xanthomonas albilineans, the causal agent of sugarcane leaf scald, is a bacterial plant pathogen that is mainly spread by infected cuttings and contaminated harvesting tools. However, some strains of this pathogen are known to be spread by aerial means and are able to colonize the phyllosphere of sugarcane before entering the host plant and causing disease. The objective of this study was to identify the molecular factors involved in the survival or growth of X. albilineans on sugarcane leaves. We developed a bioassay to test for the attachment of X. albilineans on sugarcane leaves using tissue‐cultured plantlets grown in vitro. Six mutants of strain XaFL07‐1 affected in surface polysaccharide production completely lost their capacity to survive on the sugarcane leaf surface. These mutants produced more biofilm in vitro and accumulated more cellular poly‐β‐hydroxybutyrate than the wild‐type strain. A mutant affected in the production of small molecules (including potential biosurfactants) synthesized by non‐ribosomal peptide synthetases (NRPSs) attached to the sugarcane leaves as well as the wild‐type strain. Surprisingly, the attachment of bacteria on sugarcane leaves varied among mutants of the rpf gene cluster involved in bacterial quorum sensing. Therefore, quorum sensing may affect polysaccharide production, or both polysaccharides and quorum sensing may be involved in the survival or growth of X. albilineans on sugarcane leaves.     

白条素研究进展

白条黄单胞菌((Xanthomonas albilineans (Ashby) Downson))是我国进境植物检疫性有害生物,其引起的甘蔗白条病是甘蔗上最重要的细菌病害。白条黄单胞菌产生一种高效的植物毒素/抗生素,称为白条素(Albicidin)。作为引起甘蔗白条病的致病因子,白条素通过抑制质体DNA回旋酶阻碍叶绿体分化,导致叶面出现典型的白色条纹症状,同时白条素的抗菌活性也赋予白条黄单胞菌在其定殖甘蔗过程中对抗其他细菌的竞争优势。此外,在纳摩尔浓度下,白条素对人类各种革兰氏阳性和革兰氏阴性病原细菌具有快速杀菌作用,使其成为具有潜在临床应用价值的抗菌药物。文中综述了该毒素的分子结构、传统提取方法、作用机制、生物合成基因及途径和化学合成方法及改良现状,以期为甘蔗白条病的防治及医用新型抗菌素的开发提供参考。     

Resident population of Xanthomonas campestris pv. malvacearum on cotton leaves: a source of inoculum for bacterial blight

Xanthomonas campestris pv. malvacearum was transmitted from infested seed to the cotyledons of cotton cv. Deltapine 61 seedlings at 28°C and relative humidities (RH) of 90% or 73%. A resident population was present on the first and second true leaves but not on the third true leaf of plants at either RH. There were smaller numbers of resident bacteria on fewer leaves of plants at the lower RH than on plants at the higher RH. Cotton plants grown from infested seed at 25°C and 30°C and incubated at 100% RH at different stages of growth developed bacterial blight on leaves that were in bud or partly expanded when incubated. Resident cells of this pathogen can thus invade susceptible leaves when conditions are favourable for infection. Bacterial blight developed on more plants at 30°C than at 25°C. In a field trial, X. campestris pv. malvacearum transmitted from seed was present as resident bacteria on the third leaf from the growing point during the vegetative development of the plant. Resident bacteria, which infected young leaves during rainy periods, were isolated from the bacterial blight lesions which subsequently developed.     

Xanthomonas albilineans Diversity and Identification Based on Rep-PCR Fingerprints

PCR with BOX and ERIC primers was used to analyze DNA of Xanthomonas albilineans and other bacteria associated with sugarcane. Generated fingerprints permitted clear separation of X. albilineans from other bacteria and revealed variation within the species. Good agreement between fingerprint groups and geographic origin and serovars was observed. Received: 27 July 2000 / Accepted: 21 August 2000     

Survival ofXanthomonas campestris pv.vesictoria in pepper seeds and roots in symptomless and dry leaves in non-host plants and in the soil

Summary A population ofXanthomonas campestris pv.vesicatoria developed as endophytes in the leaves and rhizosphere of apparently symptomless plants grown under mist but not under dry conditions. The pathogen survired for long periods on, and could be isolated from, the surface of infested dried seeds, inoculated sandy loam soil, dried leaves, and the rhizosphere of pepper and of other non-host plants. In addition, small numbers of the pathogen survived for 18 months in a field previously cropped with pepper diseased with bacterial scab. Healthy nursery or mature plants developed symptoms while growing in soil containing infested leaves, either buried or placed on the soil surface.     

Isolation of specific receptors from Xanthomonas albilineans cell walls for lectins-like glycoproteins of sugarcane

Abstract

Two families of sugarcane glycoproteins differing in their molecular mass have been isolated from sugarcane stalks. These glycoproteins specifically bind to cell wall receptors of Xanthomonas albilineans, a sugarcane pathogen, producing bacterial agglutination. Bound glycoproteins can be desorbed from bacterial cell walls by galactitol, a component of the glycosidic moiety of the sugarcane protein. This indicates that sugarcane glycoproteins bind through their glycosidic rest to the peptide moiety of the bacterial receptor. Several cell wall receptors have been isolated by affinity chromatography and separated by capillary electrophoresis.     

Substrate Specificity-Conferring Regions of the Nonribosomal Peptide Synthetase Adenylation Domains Involved in Albicidin Pathotoxin Biosynthesis Are Highly Conserved within the Species Xanthomonas albilineans

Albicidin is a pathotoxin produced by Xanthomonas albilineans, a xylem-invading pathogen that causes leaf scald disease of sugarcane. Albicidin is synthesized by a nonribosomal pathway via modular polyketide synthase and nonribosomal peptide synthetase (NRPS) megasynthases, and NRPS adenylation (A) domains are responsible for the recognition and activation of specific amino acid substrates. DNA fragments (0.5 kb) encoding the regions responsible for the substrate specificities of six albicidin NRPS A domains from 16 strains of X. albilineans representing the known diversity of this pathogen were amplified and sequenced. Polymorphism analysis of these DNA fragments at different levels (DNA, protein, and NRPS signature) showed that these pathogenicity loci were highly conserved. The conservation of these loci most likely reflects purifying selective pressure, as revealed by a comparison with the variability of nucleotide and amino acid sequences of two housekeeping genes (atpD and efp) of X. albilineans. Nevertheless, the 16 strains of X. albilineans were differentiated into several groups by a phylogenetic analysis of the nucleotide sequences corresponding to the NRPS A domains. One of these groups was representative of the genetic diversity previously found within the pathogen by random fragment length polymorphism and amplified fragment length polymorphism analyses. This group, which differed by three single synonymous nucleotide mutations, contained only four strains of X. albilineans that were all involved in outbreaks of sugarcane leaf scald. The amount of albicidin produced in vitro in agar and liquid media varied among the 16 strains of X. albilineans. However, no relationship among the amount of albicidin produced in vitro and the pathotypes and genetic diversity of the pathogen was found. The NRPS loci contributing to the synthesis of the primary structure of albicidin apparently are not involved in the observed pathogenicity differences among strains of X. albilineans.     

In vitro reactions of sugarcane (Saccharum SP.) plantlets inoculated with 2 strains of Xanthomonas albilineans (Ashby) Dowson

The symptoms of the leaf scald disease can be reproduced in vitro through the inoculation of sugarcane tissue culture plantlets. The pathogen is detected in the inoculated plantlet and is maintained at the surface of the base of the plantlets grown in vitro. Two strains of X. albilineans belonging to different serovars and lysovars reacted like pathotypes. The importance of the plant incubation temperature is clearly demonstrated. Further, in vitro the disease goes through the same phase of latency as in the field.     

Sugarcane glycoproteins may act as signals for the production of xanthan in the plant-associated bacterium Xanthomonas albilineans

Visual symptoms of leaf scald necrosis in sugarcane (Saccharum officinarum) leaves develop in parallel to the accumulation of a fibrous material invading exocellular spaces and both xylem and phloem. These fibers are produced and secreted by the plant-associated bacterium Xanthomonas albilineans. Electron microscopy and specific staining methods for polysaccharides reveal the polysaccharidic nature of this material. These polysaccharides are not present in healthy leaves or in those from diseased plants without visual symptoms of leaf scald. Bacteria in several leaf tissues have been detected by immunogold labeling. The bacterial polysaccharide is not produced in axenic culture but it is actively synthesized when the microbes invade the host plant. This finding may be due to the production of plant glycoproteins, after bacteria infection which inhibit microbial proteases. In summary, our data are consistent with the existence of a positive feedback loop in which plant-produced glycoproteins act as a cell-to-bacteria signal that promotes xanthan production, by protecting some enzymes of xanthan biosynthesis against from bacterial proteolytic degradation.Key words: leaf scald, infectivity, Saccharum officinarum (L.) cv. mayarí 55-14, sugarcane glycoproteins, xanthan-like polysaccharide, Xanthomonas albilineans     

甘蔗赤腐病内生拮抗菌YC89的筛选及鉴定

【目的】筛选防治甘蔗赤腐病(sugarcane red rot)的生防菌株。【方法】实验以前期分离获得的甘蔗内生细菌为目标菌,以甘蔗赤腐病的病原真菌镰孢炭疽菌(Colletotrichum falcatum Went.)为指示菌,采用平板对峙法筛选对该病菌有较强抑制作用的菌株,然后通过琼脂扩散法测定菌株代谢产物对抑菌活性的影响,并对具有较好拮抗效果的高效菌株进行抑菌广谱性分析并对其进行鉴定。最后通过形态学、生理生化特征以及16SrDNA和gyrA序列分析对高效菌株YC89进行鉴定。【结果】经初筛筛选到抑菌带均大于1.60 cm的5株拮抗细菌,其中X22、W2、YC89抑菌带均高达1.87 cm。对初筛得到的5株内生菌进行复筛,结果所示菌株YC89、H1、X22、W2、YT93对镰孢炭疽菌的抑菌率都在75%以上,其中菌株YC89对该病菌的抑菌效果最好,其抑菌率为78%。菌株YC89的发酵液、上清液、过滤液及粗蛋白提取液对镰孢炭疽菌的生长有较强的抑制作用,且菌株YC89对玉米大斑病、甘蔗梢腐病、草莓灰霉病等7种病原菌也有较好的抑制效果。通过菌株鉴定结果,初步将YC89菌株鉴定为贝莱斯芽孢杆菌(Bacillus velezensis)。【结论】菌株YC89对镰孢炭疽菌具有较好的抑制效果,表明其对甘蔗赤腐病的生物防治具有较大的应用潜力。     

Association of a phytoplasma with a yellow leaf syndrome of sugarcane in Africa

Evidence is presented for the association of a phytoplasma, provisionally named sugarcane yellows phytoplasma (ScYP), in sugarcane affected by a yellow leaf syndrome. The phytoplasma was consistently detected in leaves of more than 40 varieties from eight African countries. It was present in all symptomatic as well as some asymptomatic field grown cane samples but not in plants grown from true seed, and it was also observed in phloem sieve tubes by transmission electron microscopy. Phytoplasma 16S rDNA was confirmed by PCR, and restriction fragment analysis using Rsal and Haelll confirmed that PCR-amplified products were of phytoplasma rather than of plant or of other pathogen origin. Sequences obtained from the intergenic spacer region, between the 16S and 23S rDNA genes, confirmed the identity of the phytoplasma as belonging to the western X group of phytoplasmas.     

Transmission of Bacterium Corynebacterium michiganense pv. michiganense by Seeds

The results of experiments on transmission of Corynebacterium michiganense pv. michiganense showed that the spread of the bacterium by artificially infested seeds varies, but it was confirmed that from artificially infested seeds few diseased plants can be grown. The results depend on the environmental conditions during experimentation and the method of assaying the seedlings. High relative humidity favours the spread of the pathogen. The use of selective media helped the detection ofthe pathogen in seemingly healthy plants. It was proved that host can have population of C. michiganense pv. michiganense in a resident phase. It is assumed that when conditions are favorable the pathogen multiplies and cause disease.     

Characterisation and action mode of Gluconacin,a bacteriocin with antimicrobial activity against Xanthomonas albilineans

Gluconacin, a bacteriocin produced by Gluconacetobacter diazotrophicus PAL5, has previously shown a large spectrum of inhibitory activity against beneficial and phytopathogenic bacteria. The present study proposes a three-dimensional (3D) structure for Gluconacin based on modelling and describes some physicochemical characteristics and the effect of the peptide on cells of the phytopathogenic bacterium Xanthomonas albilineans ICMP196. The Gluconacin 3D structural model results demonstrated the 7 α-helices and 11 β-sheets. Growth inhibition of the indicator microorganism, X. albilineans, occurred in the first moments of contact with Gluconacin (0.25 μg μl^?1). Treatment of bacterial cells caused significant loss of inorganic phosphate and UV-absorbing materials. Scanning electron microscopy images showed that Gluconacin-treated X. albilineans cells were fully lysed. These results suggest that the mode of action of this peptide involves altered membrane integrity and increased permeability, resulting in complete cell lysis. Physicochemical characterisation demonstrated stability of biological activity under high temperatures, including autoclaving conditions and low pH. The activity was reduced after treatment with proteases and some surfactants and abolished with ethylenediaminetetraacetic acid (EDTA). The 3D conformation model indicates the possibility of a hydrophobic region, which could possibly interact directly with the cell membrane of target bacteria. In conclusion, the ability of Gluconacin to inhibit growth of phytopathogens of agricultural importance opens up new opportunities for biotechnological applications and, consequently, a reduction in the use of pesticides.     

Survival and Possible Spread of Erwinia amylovora and Related Plant-Pathogenic Bacteria Exposed to Environmental Stress Conditions

The fire blight pathogen Erwinia amylovora was assayed for survival under unfavourable conditions such as on nitrocellulose filters, in non‐host plants as well as in inoculated mature apples and in infested apple stem sections. In a sterile dry environment, an E. amylovora EPS (exopolysaccharide) mutant, and to a lesser extent its parental wild‐type strain decreased within 3 weeks to a low titre. However, under moist conditions the decrease of viable cells occurred only partially for both strains. Very low cell titres were recovered after application of E. amylovora onto the surface of tobacco leaves, whereas infiltration into the leaves produced lesions (hypersensitive response, HR), in which the bacteria survived in significant amounts. A similar effect was found for the necrotic zones of HR in tobacco leaves caused by E. pyrifoliae, by Pseudomonas syringae pathovars and HR‐deficient E. amylovora mutants or mutants deficient in EPS synthesis and disease‐specific genes. During 7 years of storage, the viability of E. amylovora in wood sections from fire blight‐infested apple trees declined to a low titre. In tissue of mature apples, E. amylovora cells slowly dispersed and could still be recovered after several weeks of storage at room temperature. A minimal risk of accidental dissemination of E. amylovora apart from infested host plants can experimentally not be excluded, but other data confirm a very low incidence of any long distance distribution.     

The Spread of Epiphytic Populations of Xanthomonas campestris pv. vesicatoria on Pepper in the Field

The spread of the epiphytic population of Xanthomonas campestris pv. vesicatoria and the disease it causes, bacterial leaf spot, were studied in field plots of pepper near Gainesville, Florida. In the summer of 1989, the epiphytic population of X. campestris pv. vesicatoria was dispersed to the west-northwest from point sources of diseased plants. Winds from the southeast during rainstorms were essential for the spread of bacteria in the field. In the autumn of 1989, a focus of bacterial leaf spot developed naturally near the centre of the experimental plot. The epiphytic population of X, campestris pv. vesicatoria increased sharply after a 2-day rain accompanied with strong wind. The wind was believed to be responsible for the transport of bacteria to distances 32 m from the focus. Initially in both seasons, the epiphytic populations occurred as distinct gradients from the focal sources of diseased plants. These gradients flattened over time and the disease incidence increased to near 100%, The increase in the epiphytic populations of the pathogen to > 3.0 log₁₀ (cfu cm⁻²) on healthy plants away from the foci preceded disease appearance by several weeks. Applications of cupric hydroxide plus mancozeb significantly reduced the epiphytic population of X. campestris pv. vesicatoria on pepper leaves and slowed the spread of disease in the plots.     

Origin of Early Attacks of Sclerotinia Stem Rot on Winter Oilseed Rape (Brassica napus sub. sub. sp. oleifera var. biensis) in the UK

Studies in artificially infested field plots of winter oilseed rape showed that mycelia originating from both sclerotia and ascospores of Sclerotinia sclerotiorum can initiate early attacks of sclerotinia stem rot. Disease symptoms appeared in early November in plots previously infested with sclerotia in September. There was a 6–7 week period from artificially inoculating plants with ascospores in October to observing disease symtoms in December. The primary sites of infection for both typesof inocula were the laminae and petioles of senescent and frost-damaged leaves. Following primary infection, mycelia of the pathogen spread by plant to plant contact, causing secondary infections of neighbouring plants. Sclerotia developed on diseased plants and high numbers were returned to the soil. The importance of these findings to the epidemiology of the disease are discussed.     

Pre- and post-landing response of the parasitoid Encarsia formosa to whitefly hosts on Gerbera jamesonii

One of the factors that may complicate biological control of the greenhouse whitefly on Gerbera jamesonii by Encarsia formosa is the rosette shape of this ornamental, which differs from the vertical shape of most vegetable plants (cucumber, egg plant, tomato, etc.). Therefore, host-habitat location and the behaviour prior to landing on uninfested and infested leaves was studied. Attraction of E. formosa from a short distance by infested leaves could not be detected: the parasitoid females landed at random on uninfested and infested leaves. After the first landing, a redistribution of the wasps occurred on the leaves. After 24 h three times as many wasps were found on the infested leaves than on uninfested ones. In a dispersal experiment with four plants, E. formosa appeared to have no preference for landing on leaves of the medium age class, which is the age class on which most of the whiteflies in a suitable stage for parasitism occur. Twenty percent of the parasitoids were found on the plants 20 min after releasing them. These results were independent of the plant cultivar and the host density on the plants. In the course of 8 h, the number of E. formosa females recovered from plants increased linearly, and this increase was greater on plants where hosts were present and also greater on the plant cultivar with the lowest trichome density. After 24 h, the percentage of females was highest (56%) on plants with the highest host density. E. formosa females were arrested on leaves where hosts were present. Contrary to our expectation, the results from the two G. jamesonii cultivars that differed strongly in leaf hairiness were not significantly different in most experiments. Only at the high host density was parasitism found to be lower on the cultivar with the higher hair density. Parasitoids may walk on top of the `hair coverlet' of cultivars with high trichome density and, therefore, be hampered less than expected.