Abscisic acid metabolism in Ceratocystis coerulescens

The fungus Ceratocystis coerulescens Bakshi (strain RWD 390) has been shown to produce the plant hormone, abscisic acid (ABA). The production of ABA in defined liquid medium during a culture period of 50 days was measured by gas-liquid chromatography. A considerable accumulation of ABA occurred in the stationary phase. Maximum ABA contents were 3.5 ng ml⁻¹ in culture media and 218 ng (g dry weight)⁻¹ in mycelial extracts.
The ABA-metabolizing capability of the fungus was investigated. Dihydrophaseic acid, and phaseic acid, ABA metabolites in higher plants, were not present in cultures of Ceratocystis coerulescens . When [2-¹⁴C]-ABA was fed to the fungus, the formation of [2-¹⁴C]- 2-trans , 4- trans -ABA and a second metabolite, less polar than ABA, was observed. This suggests a different metabolic pathway of ABA in the fungus.     

Stammesspezifische Acetylierungen verschiedener Alkohole bei der Gattung Ceratocystis

Zusammenfassung An sieben Arten der Gattung Ceratocystis wird das Spektrum der wasserdampfflüchtigen Stoffe und besonders der Essigsäureester untersucht. Dabei werden prinzipielle Unterschiede in der Fähigkeit festgestellt, gewisse selbstgebildete primäre und sekundäre Alkohole zu acetylieren.Diese Untersuchungen werden auf 14 Stämme von Ceratocystis coerulescens ausgedehnt. Hier kann gezeigt werden, daß die Spezifität der Acetylierungs-reaktionen gegenüber primären und sekundären Alkoholen verschiedener Kettenlänge gewisse Rückschlüsse auf die Verwandtschaft der untersuchten Stämme zuläßt.Durch Variation der Kulturbedingungen lassen sich enge Beziehungen zwischen den Acetylierungsreaktionen und dem Citronensäurecyclus nachweisen.

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Strain-specific acetylation of different alcohols in the genus Ceratocystis

Summary The steam-volatile products, especially the acetylated alcohols, of 7 Ceratocystis-species were analyzed. There are fundamental differences in the ability for acetylation of certain primary and secondary alcohols.These studies were extended to 14 strains of Ceratocystis coerulescens. From the specifity of the acetylation reactions concerning primary and secondary alcohols of different chainlength, certain conclusions can be drawn on the relationship between the strains of this study.By variation of cultural conditions it has been possible to show close connections between the acetylation reactions and the tricarboxylic acid cycle.

     

A comparison of some Ceratocystis species with sporothrix schenckii

Sympodulosporogenous states ofC. minor, C. montia, C. multiannulata, C. narcissi, C. nigrocarpa, C. perparvispora andC. pilifera were compared with typical and atypical strains ofS. schenckii from the aspects of some culture, morphological, serological characteristics, and mouse virulence. With a possible exception, all the former characteristics demonstrated among theCeratocystis species were either the same as, or varied in the same way as those observed amongS. schenckii strains. None of the former hydrolyzed starch, although all of the latter did. All species and strains cross reacted serologically in agglutination and Arthus-rype reactions, and produced similar gross pathological signs when injected with gastric mucin intraperitoneally into mice. Except for some variations in sizes and shapes of sympodulospores and of yeast-like budding forms observed in tissue smears and in cultures incubated at 37°C, theCeratocystis species were not significantly different from typical strains ofS. schenckii.

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Zusammenfassung Der sympodulosporogene Zustand vonC. minor, C. montia, C. multiannulata, C. narcissi, C. nigrocarpa, C. perparvispora undC. pilifera wurde mit typischen und atypischen Stämmen vonS. schenckii betreffs kultureller, morphologischer, serologischer Charakteristik und auf Virulenz für Mäuse untersucht. Mit einer möglichen Ausnahme waren alle Charakteristiken unter denCeratocystis-Arten dieselben oder sie wechselten wie diejenigen unter den Stämmen vonS. schenckii. Keine Stämme derCeratocystis hydrolysierten Stärke, während die Stämme vonS. schenckii getan haben. Alle die Arten und Stämme zeigten Kreuzreaktionen serologisch und in der Arthus-reaktion und zeigten dieselben groß-pathologischen Veränderungen nach intraperitonealen Injektionen mit Magenmuzin in der Maus. Außer etlicher Abwechslungen in Größe und Gestalt der Sympodulosporen und der hefe-ähnlichen Keimung, die in Gewebeausstrichen und in Kulturen bei 37°C beobachtet worden sind, waren dieCeratocystis-Arten nicht wesentlich unterschiedlich von typischen Stämmen vonS. schenckii.

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The author, Dr.R. W. Davidson (Colorado State University, Ft. Collins, Colorado), and Dr.F. Mariat (Institut Pasteur, Paris) have, in collaboration, identified the ascigerous state ofSporothrix schenckii strain G-118 isolated by the latter to beCeratocystis stenoceras (Robak)C. Moreau.     

Genomic analysis of the aggressive tree pathogen Ceratocystis albifundus

The overall goal of this study was to determine whether the genome of an important plant pathogen in Africa, Ceratocystis albifundus, is structured into subgenomic compartments, and if so, to establish how these compartments are distributed across the genome. For this purpose, the publicly available genome of C. albifundus was complemented with the genome sequences for four additional isolates using the Illumina HiSeq platform. In addition, a reference genome for one of the individuals was assembled using both PacBio and Illumina HiSeq technologies. Our results showed a high degree of synteny between the five genomes, although several regions lacked detectable long-range synteny. These regions were associated with the presence of accessory genes, lower genetic similarity, variation in read-map depth, as well as transposable elements and genes associated with host-pathogen interactions (e.g. effectors and CAZymes). Such patterns are regarded as hallmarks of accelerated evolution, particularly of accessory subgenomic compartments in fungal pathogens. Our findings thus showed that the genome of C. albifundus is made-up of core and accessory subgenomic compartments, which is an important step towards characterizing its pangenome. This study also highlights the value of comparative genomics for understanding mechanisms that may underly and influence the biology and evolution of pathogens.     

Studies on the development of perithecium of Ceratocystis stenoceras

The development of the perithecium of Ceratocystis stenoceras was observed by a light microscope and by a scanning electron microscope.The fungus has developed dark brown perithecia on wheat agar medium in three days of incubation. Perithecial primordia appeared as tightly knotted coils. At the center of it an oval ascogonium was observed. The ascogonium was developed from a lateral wall of a hypha, and the hyphae covering the ascogonium branched at the basal part where the ascogonium was attached. These hyphae branched repeatedly in the developmental growth to cover the ascogonium, and it was finally covered tightly. The plasmogamy of this fungus is much probably performed by the gametangial contact. As the stage proceeded, the ascogonium elongated, the terminal and the basal portions of it swelled and cleavage of the ascogonium resulted. Each of the cleaved ascogonia germinated continuously and stretched out the ascogenous hyphae. About that time the cells consisting of perithecia were vacuolated from the center and successively dissolved, so that a space was formed in the center of the body. Ascogenous hyphae continued to develop downwards, and their end were fixed to the inner wall of the body.The upper portion of the hyphae converged to the center of the body and the ascogenous hyphae became the supporting tissue for ascus formation.Hook formation was observed prior to the ascus formation. After completion of karyogamy by hook formation, the fissure appeared on the ascus and the end portion was released. The released portion included eight ascospores. The ascus had a smooth surface and no special structure was seen on the top. As the asci were matured, they evanesced by themselves and concurrently ascospores came out. Finally the body was massively filled with ascospores.     

MBC tolerance in aggressive and non-aggressive isolates of Ceratocystis ulmi

In selection experiments, tolerance to 0–5 ppm methyl benzimidazole-2-ylcarbamate (MBC) occurred at a frequency of c. 1 in 1–3 ×10⁸ conidia in both aggressive and non-aggressive isolates of Ceratocystis ulmi. The tolerant strains were inhibited by 5 ppm MBC, however, and attempts to select strains tolerant to 10 ppm were unsuccessful. In each of three isolates examined, tolerance remained stable after fifteen successive transfers on fungicide-free medium. Genetic control was nuclear and probably conditioned by a single gene. It is thought unlikely that the appearance of tolerant strains in nature will jeopardize the use of MBC for the control of Dutch elm disease.     

Oxidative Enzymes of Ceratocystis fimbriata Isolates Differing in Host Specificity

Eight isolates of Ceratocystis fimbriata differing in pathogenicity on sweet potato roots were compared in vitro for peroxidase, catalase and polyphenol oxidase activities. Pathogenic isolates were generally lower in specific activities of peroxidase and catalase than the nonpathogenic isolates. Cultures of pathogenic isolates were distinguished by black culture liquid compared to the yellow color of nonpathogenic isolates. No consistent differences among the isolates were apparent when the specific activity of polyphenol oxidase preparations were compared on various phenolic substrates. The peroxidase of C. fimbriata had an approximate molecular weight of 81,000 when compared with known protein standards on a column of Sephadex G-100 dextran gel. Its substrate specificity differed from horseradish peroxidase in that it was nonreactive with guaiacol.     

Calmodulin activity in yeast and mycelial phases of Ceratocystis ulmi

Abstract The yeast and mycelial phases of Ceratocystis ulmi contained roughly equivalent levels of calmodulin activity as determined by their ability to stimulate calmodulin-deficient bovine brain cAMP phosphodiesterase. This stimulation was calcium-dependent and could be inhibited by either dibucaine or trifluoperazine. Also, the concentration of dibucaine necessary to achieve the mycelium-to-yeast morphological conversion was found to be 3-fold greater in the presence of exogenous calcium. A model is presented in which only 30% of the cellular calmodulin need be complexed with calcium ions for mycelial development.     

The Formation of Coremia in Ceratocystis piceae Induced by Hexanal

Hexanal, and to a lesser degree nonanal, added in gaseous form induce coremia formation in the blue stain fungus Ceratocystis piceae (Münch) Bakshi grown in axenic agar culture. The optimum initial concentration of hexanal in the gas phase proved to be c. 2 mg/1 (2 × 10⁻⁵M). Possible ecological implications are discussed.     

Isolation of furanoterpene-containing particles from Ceratocystis fimbriata-infected sweet potato root tissue

Furanoterpene-containing particles were isolated by centrifugation on a discontinuous Ficoll density gradient from a homogenate of the non-infected tissue adjacent to the infected region of Ceratocystis fimbriata-infected sweet potato root tissue. The particles were recovered at a relatively high ratio in the 2% Ficoll fraction, in which there was no contamination by mitochondria and only little by endoplasmic reticulum judging from the distribution of the activities of their marker enzymes and electron micrographs. Each particle was enveloped in a single membrane, 7-10 nm thick.