Purification and in vitro characterization of the maltose-binding protein of the plant pathogen Xanthomonas citri

The uptake of maltose and maltodextrins in gram-negative bacteria is mediated by an ATP-dependent transport complex composed of a periplasmic maltose-binding protein (MBP) and membrane-associated proteins responsible for the formation of a membrane pore and generation of energy to drive the translocation process. In this work, we report the purification and in vitro functional analysis of MBP, encoded by the malE gene, of the plant pathogen Xanthomonas citri, responsible for the canker disease affecting citrus plants throughout the world. The X. citri MBP is composed of 456 amino acids, displaying a low amino acid identity (16% throughout the sequence) compared to the Escherichia coli K12 ortholog. The X. citri malE gene was cloned into a pET28a vector, and the encoded protein was expressed and purified by affinity chromatography as a His-tag N-terminal fusion peptide produced by the E. coli BL21 strain. Enhanced levels of soluble protein were achieved with static cultures kept overnight at 23 degrees C. Ability to bind immobilized amylose, the emission of intrinsic fluorescence and circular dichroism spectra indicated that the purified recombinant protein preserved both conformation and biological activity of the native protein. The availability of the recombinant MBP will contribute to the functional and structural analysis of the maltose and maltodextrin uptake system of the plant pathogen X. citri.     

The molybdate-binding protein (ModA) of the plant pathogen Xanthomonas axonopodis pv. citri

The modABC operon of phytopathogen Xanthomonas axonopodis pv. citri (X. citri) encodes a putative ABC transporter involved in the uptake of the molybdate and tungstate anions. Sequence analyses showed high similarity values of ModA orthologs found in X. campestris pv. campestris (X. campestris) and Escherichia coli. The X. citri modA gene was cloned in pET28a and the recombinant protein, expressed in the E. coli BL21 (DE3) strain, purified by immobilized metal affinity chromatography. The purified protein remained soluble and specifically bound molybdate and tungstate with K(d) 0.29+/-0.12 microM and 0.58+/-0.14 microM, respectively. Additionally binding of molybdate drastically enhanced the thermal stability of the recombinant ModA as compared to the apoprotein. This is the first characterization of a ModA ortholog expressed by a phytopathogen and represents an important tool for functional, biochemical and structural analyses of molybdate transport in Xanthomonas species.     

Differences in esterase isozymes between Panonychus citri populations infesting citrus and Osmanthus

Gene frequencies were investigated in the -Est1 locus between Japanese populations of Panonychus citri occurring on some fruit trees and on the garden trees, Osmanthus trees and Ilex crenata. A new allele, A ₃, was found in the -Est1 of populations collected on Osmanthus trees. Populations on I. crenata, Citrus unshiu and Pyrus serotina had one or both A ₁ and A ₂ alleles. However, the populations on Osmanthus trees had only the A ₃ allele and did not vary geographically.     

Alternaria mycotoxins in black rot lesion of tomato fruit: Conditions and regulation of their production

Alternaria represents the most common decay organism of the post-harvest tomato fruit. The prevalent type of decay, black rot lesion, is caused byA. alternata which may invade tomato tissue damaged by sun scald.Aspergillus niger, A. flavus andRhizopus stolonifer come in the second count level and occupy high to moderate occurrence. The mainly natural mycotoxins produced in rotted tomato are alternariol (AOH), alternariol monomethyl ether (AME), and tenuazonic acid (TA). Altertoxin I & II (AT-I & AT-II), in addition to AOH, AME and TA were produced by localA. alternata in a synthetic medium. The optimum temperature for toxin production byA. alternata IMI 89344 was 28 °C for AOH and AME, 21 °C for TA, and 14 °C for AT-I and AT-II. The growth and toxin were produced in a noticeable amount at 7 °C but drop at 35 °C. Significant inhibition in these toxins was attained at 500 ppm cinnamon oil in YES-Czapeks medium and in a tomato homogenate.     

The characterization of the soybean polygalacturonase-inhibiting proteins (Pgip) gene family reveals that a single member is responsible for the activity detected in soybean tissues

Polygalacturonase-inhibiting proteins (PGIPs) are leucine-rich repeat (LRR) proteins that inhibit fungal endopolygalacturonases (PGs). They are encoded by multigene families whose members show functional redundancy and subfunctionalization for recognition of fungal PGs. In order to expand the information on the structure and functional features of legume PGIP, we have isolated and characterized four members of the soybean Pgip gene family and determined the properties of the encoded protein products. Sequence analysis showed that these genes form two clusters: one cluster of about 5 kbp containing Gmpgip1 and Gmpgip2, and the other containing Gmpgip3 and Gmpgip4 within a 60 kb fragment of a separate BAC clone. Sequence diversification of the four members resides mainly in the xxLxLxx region that includes residues forming the β-sheet B1. When compared with other legume Pgip genes, Gmpgip3 groups with the bean genes Pvpgip1 and Pvpgip2, suggesting that these genes are closer to the ancestral gene. At the protein level, only GmPGIP3 shows the capability to inhibit fungal PGs. The spectrum of inhibition of GmPGIP3 against eight different fungal PGs mirrors that of the PGIP purified from soybean tissues and is similar to that of the bean PvPGIP2, one of the most efficient inhibitors so far characterized. We also report that the four Gmpgip genes are differentially regulated after wounding or during infection with the fungal pathogen Sclerotinia sclerotiorum. Following fungal infection Gmpgip3 is up regulated promptly, while Gmpgip2 is delayed.     

The grapevine polygalacturonase-inhibiting protein (VvPGIP1) reduces Botrytis cinerea susceptibility in transgenic tobacco and differentially inhibits fungal polygalacturonases

Polygalacturonase-inhibiting proteins (PGIPs) selectively inhibit polygalacturonases (PGs) secreted by invading plant pathogenic fungi. PGIPs display differential inhibition towards PGs from different fungi, also towards different isoforms of PGs originating from a specific pathogen. Recently, a PGIP-encoding gene from Vitis vinifera (Vvpgip1) was isolated and characterised. PGIP purified from grapevine was shown to inhibit crude polygalacturonase extracts from Botrytis cinerea, but this inhibitory activity has not yet been linked conclusively to the activity of the Vvpgip1 gene product. Here we use a transgenic over-expression approach to show that the PGIP encoded by the Vvpgip1 gene is active against PGs of B. cinerea and that over-expression of this gene in transgenic tobacco confers a reduced susceptibility to infection by this pathogen. A calculated reduction in disease susceptibility of 47–69% was observed for a homogeneous group of transgenic lines that was statistically clearly separated from untransformed control plants following infection with Botrytis over a 15-day-period. VvPGIP1 was subsequently purified from transgenic tobacco and used to study the specific inhibition profile of individual PGs from Botrytis and Aspergillus. The heterologously expressed and purified VvPGIP1 selectively inhibited PGs from both A. niger and B.␣cinerea, including BcPG1, a PG from B. cinerea that has previously been shown to be essential for virulence and symptom development. Altogether our data confirm the antifungal nature of the VvPGIP1, and the in vitro inhibition data suggest at least in part, that the VvPGIP1 contributed to the observed reduction in disease symptoms by inhibiting the macerating action of certain Botrytis PGs in planta. The ability to correlate inhibition profiles to individual PGs provides a more comprehensive analysis of PGIPs as antifungal genes with biotechnological potential, and adds to our understanding of the importance of PGIP:PG interactions during disease and symptom development in plants.Dirk A. Joubert and Ana R. Slaughter contributed equally to this work.     

Biological control of citrus mealybug,Planococcus citri with an introduced parasite,Leptomastix dactylopii in India

Planococcus citri (Risso) is one of the major pests of citrus orchards in India. For the control ofP. citri, an encyrtid parasite,Leptomastix dactylopii How. was introduced from West Indies in 1983. The parasite was mass bred and inoculative releases were made in 2 selected citrus orchards where infestation of mealybug on fruits (sweet orange, seedless lime and acid lime) ranged from 38 to 65 per cent. Establishment of the parasite in the 2 release orchards resulted in complete control of the mealybug within 3 to 4 months. No insecticidal sprays were required subsequently for the control ofP. citri in the following seasons. Contribution No. 152/85 of the IIHR, Bangalore — 560089.     

Management of Prays citri in lemon orchards by mass trapping of males

Preliminary field trials on the control of Prays citri (Millière) (Lepidoptera: Yponomeutidae) by mass trapping were carried out from 1976 using synthetic sex pheromone (Z-7-tetradecenal) baited traps. A clear tendency was revealed for a reduction in flower infestation by the larvae of this pest, providing that the minimum required number of traps (120 per ha) were employed and maintained throughout the entire year. In 1980–1983, commercial field trials were conducted over 30 ha of lemon trees. Rubber septa dispensers were loaded with 0.5–0.6 mg synthetic pheromone and refilled every four months. For comparison, about 30 ha lemon trees were sprayed 3–6 times a year with an organophosphate (azinphos-methyl) insecticide treatment. One plot of 0.22 ha was used as control. Results from all three areas were compared for mean male catch per trap per day, mean number of moths emerging per flower, and fruit yield for the two years prior to the trials and the three years of the trials in all plots. Lemon trees without control measures showed a decline in fruit yield. Controlling the moth by mass trapping of males, was significantly (P<0.05) cheaper and somewhat more efficient than spraying 3–6 times/year with insecticides.

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Résumé Des essais préliminaires de lutte contre P. citri Millière (Lep. Yponomeutidae) par piégeage de masse ont été menés en 1976 en utilisant la phéromone sexuelle (Z-7-tétradécénal) comme appât. On a observé une nette tendance à la réduction de l'infestation des fleurs par les chenilles a été observée lorsque le nombre nécessaire de pièges (120/ha) a été maintenu toute l'année. En 1980–83 des essais commerciaux ont été réalisés sur un verger de 30 ha de citronniers. Des diffuseurs rubber septa étaient remplis avec 0,5–0,8 mg phéromones synthétiques et rechargés tous les 4 mois. Par comparaison, un verger de 30 ha a été pulvérisé 3 à 6 fois par an avec un organophosphate (méthyle d'Azinphos). Le témoin était constitué par une parcelle de 0,22 ha. Les captures moyennes quotidiennes de mâles par piège, le nombre de papillons obtenus par fleur e les récoltes de fruits pendant les 2 années précédant ces interventions et les 3 années de durée des traitements ont permis de comparer la situation sur les 3 aires. Les citronniers témoins ont présenté une diminution de production de fruits. La protection par le piégeage massif des mâles est significativement moins chère (P<0,05) et semble plus efficace que 3 à 6 traitements insecticides par an.

     

Alternaria brasiliensis sp. nov., a leaf pathogen on Phaseolus vulgaris

Alternaria brasiliensis sp. nov., was isolated from leaves of common bean, Phaseolus vulgaris L., showing punctiform non concentric leaf spots of brown color. Besides the symptomatological differences, the new Alternaria species presents distinct type of arrangement of conidia chain, body and beak size. The disease was observed in Montanha county, State of Espirito Santo, Brazil, but not yet reported in the literature. The causal agent of the disease is now described by the first time. The epithet used here is referring to the country where the species has been found. This revised version was published online in June 2006 with corrections to the Cover Date.     

Detection of a Concanavalin A binding protein in the mollicute Spiroplasma citri and purification from the plasma membrane

A protein that binds Concanavalin A (Con A) was detected on Western blots of Spiroplasma citri proteins. Its apparent molecular weight was 84000. It was localized in the plasma membrane. Affinity chromatography on Con A-agarose was used to isolate this protein. The glycosylation inhibitor, tunicamycin, inhibits S. citri growth and seems to block the glycosylation of the Con A-binding protein.     

Suitability of Asian citrus psyllid, Diaphorina citri, as prey for ladybeetles

Given the apparent importance ofladybeetles as biological control agents of theinvasive Asian citrus psyllid, Diaphorinacitri Kuwayama (Homoptera: Psyllidae), aseries of experiments were undertaken to assessthe nutritional suitability of this pest as aprey item. Five species of Coccinellidae wereshown to develop successfully on a diet ofpsyllid nymphs and four species produced viableeggs. Eggs of the flour moth, Ephestiakuehniella Zeller (Lepidoptera: Pyralidae)were used as a reference diet. Larvae of Curinus coeruleus Mulsant, Cyclonedasanguinea L., Exochomus childreniMulsant, Harmonia axyridis Pallas, andOlla v-nigrum Mulsant all had survival ona diet of D. citri nymphs not differentfrom 100%, although developmental times wereextended and adult dry weights were reducedrelative to the Ephestia egg diet. Species were ranked (highest to lowest) forlarval performance on the D. citri dietrelative to the Ephestia egg diet as:E. childreni, 0.85;O. v-nigrum,0.82; C. coeruleus, 0.80;H.axyridis, 0.71;C. sanguinea, 0.48. Most females of C. sanguinea ceasedoviposition on the second day followingtransferal to the D. citri diet, but thefecundity and fertility of females of the otherspecies were not different from those feedingon Ephestia eggs. Generation times onthe Ephestia egg diet at 24°C(time to egg hatch + larval developmental time+ pupation time + adult prereproductive period)were (mean ± SEM): C. coeruleus, 56.7± 1.32 d;C. sanguinea, 28.0 ±0.88 d;E. childreni, 60.8 ± 1.96 d;H. axyridis, 32.2 ± 1.47 d;O.v-nigrum, 25.8 ± 1.12 d. Adult females ofC. coeruleus, H. axyridis and O.v-nigrum consumed the most psyllids in oneh, C. sanguinea was intermediate, andE. childreni consumed the least.     

Increases in densities of the citrus red mite,Panonychus citri [Acarina: Tetranychidae], in association with the Argentine ant,Iridomyrmex humilis [Hymenoptera: Formicidae], in southern California citrus

We monitored the activities of the Argentine ant,Iridomyrmex humilis (Mayr), in 3 citrus orchards during 1984 and 1985. We also monitored densities of citrus red mite,Panonychus citri (McGregor), the adult spider mite destroyer,Stethorus picipes Casey [Col.: Coccinellidae], and the predatory mite,Euseius tularensis Congdon [Acarina: Phytoseiidae] during the same period in ant-present and ant-free plots in each orchard. I. humilis was excluded for at least 9 months from trees pruned 60 cm from the ground following a basal application of 1 or 2 % chlorpyrifos 4 EC. Autumn densities ofP. citri in these ant-free plots were significantly lower than those in the plots infested withI. Humilis. S. picipes appeared to be the most important predator, maintaining lowP. citri densities on citrus in southern California in the absence ofI. humilis activity.S. picipes densities increased numerically in response to the early spring and late autumn increases in the density ofP. citri populations. However, in the presence ofI. humilis activity, effective predation was apparently inhibited. Densities ofE. tularensis were unaffected by the presence ofI. humilis, nor didE. tularensis respond to spring or autumn increases in the density ofP. citri populations in any of the orchards.      

昆明美人蕉黑斑病菌——链格孢Alternaria alternata

美人蕉是重要的园林绿化植物和生物资源。为了明确美人蕉黑斑病的病原菌种类,并为病害防治提供理论指导,调查了昆明市美人蕉黑斑病的发生情况,采用组织分离法对病原物进行了分离和纯化,并进行了致病性测定。通过形态学和rDNA ITS序列分析,将昆明美人蕉黑斑病的病原菌鉴定为链格孢Alternaria alternata。     

The citrus plant pathogen Xanthomonas citri has a dual polyamine-binding protein

ATP-Binding Cassette transporters (ABC transporters) are protein complexes involved in the import and export of different molecules, including ions, sugars, peptides, drugs, and others. Due to the diversity of substrates, they have large relevance in physiological processes such as virulence, pathogenesis, and antimicrobial resistance. In Xanthomonas citri subsp. citri, the phytopathogen responsible for the citrus canker disease, 20% of ABC transporters components are expressed under infection conditions, including the putative putrescine/polyamine ABC transporter, PotFGHI. Polyamines are ubiquitous molecules that mediate cell growth and proliferation and play important role in bacterial infections. In this work, we characterized the X. citri periplasmic-binding protein PotF (XAC2476) using bioinformatics, biophysical and structural methods. PotF is highly conserved in Xanthomonas sp. genus, and we showed it is part of a set of proteins related to the import and assimilation of polyamines in X. citri. The interaction of PotF with putrescine and spermidine was direct and indirectly shown through fluorescence spectroscopy analyses, and experiments of circular dichroism (CD) and small-angle X-ray scattering (SAXS), respectively. The protein showed higher affinity for spermidine than putrescine, but both ligands induced structural changes that coincided with the closing of the domains and increasing of thermal stability.     

Cutaneous Phaeohyphomycosis due to Alternaria Infectoria

Here we report a case of cutaneous alternariosis in a 74-year-old man treated by corticotherapy for myasthenia, and presenting with papular, crusted lesions on the left elbow and the right knee. Histological examination of the biopsy specimens showed fungal hyphae associated with round-shaped cells which were highly suggestive of alternariosis. Mycological culture allowed the isolation of a dematiaceous fungus which was identified as a member of the Alternaria infectoria species-group. This was confirmed by PCR amplification and sequencing of the internal transcribed spacer domain of the gene encoding nuclear ribosomal DNA and of the mitochondrial small subunit ribosomal DNA domain. The fungus was therefore referred to the Scientific Institute of Public Health where it was identified as Alternaria infectoria, on the basis of its very small 1 or 2-celled conidia often arranged in long chains and presenting with very long secondary conidiophores. Corticotherapy was stopped and a local antifungal treatment with ketoconazole was initiated, allowing the stabilisation of the cutaneous lesions within 2 months.     

Morphological description of the mouthparts of the Asian citrus psyllid, Diaphorina citri Kuwayama (Hemiptera: Psyllidae)

Scanning (SEM) and transmission (TEM) electron microscopy were used to elucidate the morphology of the rostrum, as well as the mandibular and maxillary stylets of the psyllid Diaphorina citri, vector of phloem-inhabiting bacteria associated with citrus huanglongbing (HLB) disease. D. citri has a cone-shaped rostrum that extends behind the pair of prothoracic coxae. The stylet bundle comprises a pair of mandibular (Md) and maxillary (Mx) stylets with a mean length of 513.3 μm; when retracted, their proximal portions form a loop and are stored in the crumena (Cr). Serial cross-sections of the rostrum revealed that the mandibles are always projected in front of the maxillary stylets. The two maxillary stylets form the food and salivary canals, with diameters of 0.9 μm and 0.4 μm respectively. These two canals merge at the end of the stylets forming a common duct with a length of 4.3 μm and a mean diameter of 0.9 μm. The acrostyle, a distinct anatomical structure present in the common duct of aphid maxillary stylets, was not observed by TEM in the ultrathin cross-sections of the common duct (CD) of D. citri. This study provides new information on D. citri mouthparts that may help to understand the feeding behaviour of this important vector of HLB-associated bacteria.     

Cloning and characterization of three hypothetical secretion chaperone proteins from Xanthomonas axonopodis pv. citri

Xanthomonas axonopodis pv. citri (Xac) causes citrus canker in plantations around the world and is of particular significance in Brazil where its incidence has risen exponentially over the past decade. Approximately one third of the predicted Xac open reading frames show no homology, or homology with very low score with that of known sequences. It is believed that Xac utilizes secretion systems to transfer virulence proteins into susceptible eukaryotic cells. This process is assisted by secretion chaperones that maintain virulence proteins partly or completely unfolded during translocation. We have cloned three of these hypothetical secretion chaperones: XAC0419 and XAC1346 from type III secretion system (TTSS) and XACb0033 from type IV secretion system (TFSS). All proteins were cloned in a pET23a vector (Novagen), expressed at 37 degrees C using a BL21(DE3)pLysS Escherichia coli strain and purified by ion exchange and gel-filtration chromatographic methods. Pure proteins were characterized using spectroscopic measurements: circular dichroism, and both static and lifetime emission fluorescence in the case of XACb0033. The analyzed proteins are stable at elevated temperatures (up to 65 degrees C) and exhibit alpha-helix content from approximately 30% (XACb003) to approximately 87% (XAC1346). XACb0033 exhibits lifetimes in the fluorescence experiments that indicate different neighborhoods for its tryptophan residues. These chaperones have the characteristics of TTSS and TFSS: all are small, with a high alpha-helix content, and without ATP-binding or ATP-hydrolyzing activity.     

Fungicidal synergistic effect of biogenically synthesized zinc oxide and copper oxide nanoparticles against Alternaria citri causing citrus black rot disease

Citrus black rot disease being caused by Alternaria citri is a major disease of citrus plants with 30–35% economic loss annually. Fungicides had not been effective in the control of this disease during last few decades. In the present study, antifungal role of green synthesized zinc oxide (ZnO) and copper oxide (CuO) nanoparticles (NPs) were studied against Alternaria citri. Alternaria citri was isolated from disease fruits samples and was identified by staining with lacto phenol cotton blue. Furthermore, CuO and ZnO NPs were synthesized by utilizing the lemon peels extract as the reducing and capping agent. Nanoparticles were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. From the XRD data, the calculated size of CuO NPs was to be 18 nm and ZnO NPs was16.8 nm using Scherrer equation. The SEM analyses revealed the surface morphology of all the metal oxide NPs synthesized were rounded, elongated and or spherical in the shape. The zone of inhibition was observed to be 50 ± 0.5 mm by CuO NPs, followed by 51.5 ± 0.5 mm by ZnO NPs and maximum zone of antifungal inhibition was observed to be 53 ± 0.6 mm by mix metal oxide NPs. The results of minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of the synthesized nanoparticles showed that at the certain concentrations (80 mg ml^?1), these NPs were capable of inhibiting the fungal growth, whereas above that specified concentrations (100 mg ml^?1), NPs completely inhibited the fungal growth. Based on these findings, the green synthesized NPs can be used as alternative to fungicide in order to control the citrus black rot disease.