Kinds Of Spores Research Articles

Surface-Imprinted Polysiloxane with Recognition Ability Based on an ITO Layer for Rapid Detection of Fusarium oxysporum f. sp. cubense by the Naked Eye.

Direct observation by the naked eye of fluorescence-stained microbes adsorbed on surface imprinted polymers (SIPs) is highly challenging and limited by speed, accuracy and the semiquantitative nature of the method. In this study, we tested for the presence of spores of Fusarium oxysporum f. sp. cubense race 4 (Foc4), which cause severe banana Fusarium wilt disease and reduces the area of banana plants. This kind of spore can become dormant in soil, which means that the detection of secreted molecules (molecular imprinting) in soil may be inaccurate; detection methods such as polymerase chain reaction (PCR) and Raman spectroscopy are more accurate but time-consuming and inconvenient. Therefore, a semiquantitative and rapid SIP detection method for Foc4 was proposed. Based on the ITO conductive layer, a reusable and naked-eye-detectable Foc4-PDMS SIP film was prepared with a site density of approximately 9000 mm-2. Adsorption experiments showed that when the Foc4 spore concentration was between 104 to 107 CFU/mL, the number of Foc4 spores adsorbed and the fluorescence intensity were strongly correlated with the concentration and could be fully distinguished by the naked eye after fluorescence staining. Adsorption tests on other microbes showed that the SIP film completely recognized only the Foc series. All the results were highly consistent with the naked-eye observations after fluorescence staining, and the results of the Foc4-infected soil experiment were also close to the ideal situation. Taken together, these results showed that Foc4-PDMS SIPs have the ability to rapidly and semiquantitatively detect the concentration of Foc in soil, which can provide good support for banana cultivation. This method also has potential applications in the detection of other fungal diseases.

Microstructure characterization of different types of chlamydospores in Arthrobotrys flagrans.

The morphological and structural differences of different types of chlamydospore of Arthrobotrys flagrans, a nematophagous fungus, were studied under light microscope and electron microscope to provide a reference for the biological control of parasitic nematodiasis. In this study, A. flagrans isolate F088 dormant chlamydospore and nondormant chlamydospore were selected as the research objects. The structural differences of these spores were observed by optical microscopy through lactol cotton blue, Trypan blue, and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) staining. FunXite -1, 4',6-diamidino-2-phenylindole, and calcofluor white staining were used to observe the metabolic activity, cell wall, and nucleus differences of the two types of spores under fluorescence microscope. Ultrastructure of the two kinds of spores was observed using scanning electron microscope (SEM) and transmission electron microscope (TEM). Since lacto phenol cotton blue, trypan blue staining cannot distinguish dormant spores from dead spores, MTT assay was performed. Fluorescence microscopy observation showed that the cytoplasmic metabolic activity of nondormant spores was stronger than that of dormant spores. The nucleus of dormant spores was bright blue, and their fluorescence was stronger than that of nondormant spores. The cell wall of nondormant spores produced stronger yellow-green fluorescence than that of dormant spores. Ultrastructural observation showed that there were globular protuberances on the surface of the two types of spores but with no significant difference between them. The inner wall of dormant spore possesses a thick zona pellucida with high electron density which was significantly thicker than that of nondormant spores, and their cytoplasm is also changed. In this study, the microstructure characteristics of dormant and nondormant chlamydospores of A. flagrans fungi were preliminarily clarified, suggesting that the state of cell wall and intracellular materials were changed after spores entered to dormancy.

Heterosporangia in Isoetes Pantii (Isoetaceae, Pteridophyta): Revealing the Beginnings of Heterospory and Recalling Paleozoic Ancestors?

Abstract The extant plant genus Isoetes (Isoetaceae; lycophyte, quillwort) is important from an evolutionary point of view. Species of this heterosporous genus are small herbs (up to 50 centimeters) and exhibit some morphological, anatomical and embryological features of their Paleozoic arborescent lycopsid ancestors. The species Isoetes pantii produces three kinds of microspores (monolete, alete and trilete) and two types of trilete megaspores in one and the same heterosporangium. We attempt to associate these unusual functional megaspores with various Paleozoic spores described mainly from Devonian barinophytaleans such as Omniastrobus dawsonii, Barinophyton richardsonii, B. citrulliforme and Protobarinophyton pennsylvanicum. These have two kinds of spores in a sporangium and provide the first palynological evidence of heterospory at 405 Ma. The germination of microspores and megaspores and production of gametophytes within the heterosporangia of I. pantii corresponds with that of some of its Paleozoic ancestors. Retention of megaspores within heterosporangia and their germination in situ offers evidence that I. pantii exhibits the probable route of evolution of the seed habit. These observations support the hypothesis that a typical heterosporangium was the cradle for the evolution of heterospory.

Development and Evaluation of Antibacterial Microsphere using Ionotropic Gelation Method

Nisin is a bacteriocin produced through Group N streptococci consisting of Lactobacillus lactis[1], Nisin is lively most effective in opposition to Gram-positive micro organism and is considered as a bacteriocin due to the fact it is a polypeptide with inhibitory action against intently associated species. Its action has not been completely elucidated. The Gram negative organisms are insusceptible through distinctive feature of the outer membrane performing as a permeability barrier and it seems that cytoplasmic membrane disruption is the main goal in non-sporulating Gram-positive micro organism [1] even though peptidoglycan synthesis is inhibited [121] Nisin does not activate bacterial spores however, it enhances the thermal sensitivity of spores & in outgrowth of surviving no with heat . It does not prevent germination however germinated spores are sensitive to the bacteriocin [2]. Other bacteriocins are known, which includes subtilin [3]. This also inhibits outgrowth and enhances heat methods against a few kinds of spores [4]. Its mechanism of action and also the premise for differing responses of spores, and of germinating and outgrowing spores, stay speculative. Tylosin may be a macrolide made through actinomycete fradiae[5]. it's not sporicidal; it will increase the sensitivity of spores to heat and notably to ionising .

Identification of causal agent of wilt of common sage (Salvia officinalis L.)

Summary Introduction: Common sage is cultivated in Europe and North America. It has strong antiviral, antibacterial and antifungal properties. This plant can be infected by different pathogenic fungi species, such as Alternaria alternata, Fusarium spp. (F. culmorum, F. equiseti, F. oxysporum), Phomopsis sclarea and Botrytis cinerea. Those species are the most frequently isolated fungi from sage stem base. Objective: The aim of this study was to identify the causal agent of common sage wilt disease. Methods: Studies were carried out in 2018–2020. 23 fungal isolates were identified based on their morphology and with use of PCR technique. Length and width of 100 conidia growing on SNA medium were measured after 7 days. Koch’s postulates were checked and the development of one fungus isolate (no. 13) was compared on seven media: the CMA, MEA, OA, PCA, SNA, PDA and Czapek medium. Sequences of the second largest subunit of RNA polymerase II (RPB2) were used to identify the pathogen. Results: The fungus formed 3 kinds of spores: thin-walled, hyaline, slightly folded at the base, mostly 4-cell macroconidia, oblong, hyaline one- or two-cell microconidia and oval thick-walled chlamydospores. The Koch’s postulates were fulfilled. The fungus formed the most abundant aerial mycelium on the Czapek medium, and the least on the CMA medium. On the SNA medium, the mycelium grew into the medium and the aerial mycelium was not formed. The obtained RPB2 nucleotide sequence was 100% similar to the Fusarium oxysporum sequence deposited in GenBank (NCBI). Conclusions: The results of this research can be used in further studies on the biological diversity of this species.

RNA-seq between asexual archeospores and meiosis-related conchospores in Neopyropia yezoensis using Smart-seq2.

In the life cycle of Neopyropia yezoensis, a potential model system for marine macroalgae, both asexual archeospores and meiosis-related conchospores develop into thalli (gametophyte). To understand this special life phenomenon in macroalgae, we picked out the two kinds of spores (10-30 cells in each sample) and conducted RNA-seq using Smart-seq2. Comparative analysis showed that light capture and carbon fixation associated differentially expressed genes (DEGs) were upregulated in archeospores, thus indicating that archeospores are in a state of rapid vegetative growth. In conchospores, protein synthesis and degradation, especially molecular chaperone, associated DEGs were up-regulated, indicating that complex life activities might be occurring in conchospores. There were 68 genes related to DNA replication and repair expressed in conchospores, showing that active DNA replication might occur in conchospores. Moreover, we found that one conchospore specifically expressed DEG (py04595: DNA helicase) only in diploid stages (conchocelis, sporangial filament) and three archeospores specifically expressed DEGs only in haploid stages (thalli). These molecular level results indicated that conchospores were closer to diploid, and might be the meiotic mother cells of N.yezoensis. In addition, we found that the knotted-like homeobox gene (PyKNOX), which might relate to the transition of gametophyte from sporophyte, was only expressed insporophyte generation but not expressed in conchospores, archeospores and thalli, indicating the morphogenesis of gametophyte sin N.yezoensis might require the inactivation of PyKNOX.

ISOLATION AND IDENTIFICATION OF PHYTOPATHOGENIC FUNGI FROM INFECTED PLANT PARTS

Objective: The present study deals with the isolation and identification of phytopathogenic fungi. The fungal isolates were Alternaria spp (Tomato early blight), Fusarium oxysporum (Fusarium wilt), Fusarium solani (daming off and root rot), Aspergillus flavus (Ear rot) and Collectotricumspp (Anthracnose).Methods: They were isolated from infected plant parts and were identified on the basis of colony morphology andlacto phenol cotton blue (LPCB) stains were used to identifymicroscopic examination of spore structures. Pure cultures of the isolates were sub cultured and transferred onto differential media; potato dextrose agar, malt extract agar, czapek yeast extract agar and czapek dox agar for species identification using macro morphological characteristicsThe morphological characteristics of these fungal elements showed various kinds of spores have been identified up to genus/species level.Results: This study proves rapid and less expensive techniques to validate a primary alarm of contamination.Conclusion: The fivefungus which were isolated from different plant parts were very effective in distruction of the plant and found that the producionwere reduced due to the infection. This rapid and less expensive techniques to validate a primary alarm of contamination.

Integration of Membrane Distillation with solar photo-Fenton for purification of water contaminated with Bacillus sp. and Clostridium sp. spores

Although Membrane Distillation (MD) has been extensively studied for desalination, it has other applications like removing all kinds of solutes from water and concentrating non-volatile substances. MD offers the possibility of producing a clean stream while concentrating valuable compounds from waste streams towards their recovery, or emerging contaminants and pathogens present in wastewater in order to facilitate their chemical elimination. This paper analyses the elimination of bacterial spores from contaminated water with MD and the role of MD in the subsequent treatment of the concentrate with photo-Fenton process. The experiments were performed at Plataforma Solar de Almería (PSA) using a plate and frame bench module with a Permeate Gap Membrane Distillation (PGMD) configuration. Tests were done for two different kinds of spores in two different water matrixes: distilled water with 3.5wt% of sea salts contaminated with spores of Bacillus subtilis (B. subtilis) and wastewater after a secondary treatment and still contaminated with Clostridium sp. spores. An analysis of the permeate was performed in all cases to determine its purity, as well as the concentrated stream and its further treatment in order to assess the benefits of using MD. Results showed a permeate free of spores in all the cases, demonstrating the viability of MD to treat biological contaminated wastewater for further use in agriculture. Moreover, the results obtained after treating the concentrate with photo-Fenton showed a shorter treatment time for the reduction of the spore concentration in the water than that when only photo-Fenton was used.

Uptake and levels of the antibiotic berberine in individual dormant and germinating Clostridium difficile and Bacillus cereus spores as measured by laser tweezers Raman spectroscopy.

Spores of Clostridium difficile and Bacillus cereus are major causes of nosocomial diarrhoea and foodborne disease. Our aim was to measure the dynamics of the uptake of the antibiotic berberine by individual germinating spores and the levels of berberine accumulated in germinated spores. Laser tweezers Raman spectroscopy (LTRS) and differential interference contrast microscopy were used to measure levels of berberine accumulated in single germinating spores and to monitor berberine uptake and germination of individual C. difficile and B. cereus spores. MIC values of berberine for C. difficile and B. cereus spores were 640 and 256 mg/L, respectively. Levels of berberine accumulated at the berberine MICs in individual germinated spores were heterogeneous, with values of 17.1 ± 5.4 and 12.7 ± 5.5 g/L for C. difficile and B. cereus spores, respectively. These values were 25-50-fold higher than the MIC values. However, berberine did not affect the germination of C. difficile and B. cereus spores, but did block germinated spores' outgrowth. Berberine uptake kinetics were similar for these two kinds of spores. After the addition of germinants, berberine began to enter germinating spores at the time (Tlag) when rapid release of the spore core's large depot of the 1:1 chelate of Ca(2+) with dipicolinic acid began, and the level of berberine taken up was maximal shortly after spore cortex lysis was completed (Tlysis). LTRS can be used to measure uptake and levels of berberine in single cells. High levels of berberine can enter spores of C. difficile and B. cereus soon after germination is initiated, thus inhibiting spore outgrowth and minimizing hazards posed by germinated spores.

A taxonomic study of o strain of Trichosporon beigelii (Küch. et Rabenh.) Vuillemin from the soil

The morphology and physiology of a strain of <i>Trichosporon</i> beigelii was studied. Several kinds of spores and conidial stalks were observed. The observations indicate morphological characteristics should be used as positive and negative criteria in Identification of species of <i>Trichosporon</i> and in distinguishing it from related genera.

Morphological and ultrastructural description of Pleistophora dammami sp. n. infecting the intestinal wall of Saurida undosquamis from the Arabian Gulf, Saudi Arabia

Pleistophora dammami sp. n. is described from Saurida undosquamis from the Arabian Gulf in Saudi Arabia. Infection appeared as whitish cysts in the intestinal wall. Cysts ranged in size from 1 to 4 mm. The prevalence of the infection across both fish sexes was 17.5% (24/420). Two kinds of spores were recognized, microspores and macrospores, and each were ovoid in shape. The microspores measured ~2.5 × 2.0 μm in size, while the macrospores measured ~6.0 × 3.0 μm. Ultrastructurally, the parasite did not form xenoma but it formed cysts surrounded by thick cyst wall. All stages of development as meronts, sporonts, sporoblast and spores occurred in the cytoplasm of the host cells within sporophorous vesicles. The stages of development occurred asynchronously and thus all stages were randomly distributed within the cysts. Meronts were elliptical and multinucleated, with unpaired nuclei which constantly divided giving rise to new sporonts. During the transition to sporonts, the border of the meronts increased in thickness to form dense discontinuous cell coat. Later, the sporont divided into sporoblast cells which gradually differentiated the typical organelles of the spores. In mature spores, the polar filament was arranged in 20-24 coils in two rows either side of the posterior vacuole. All ultrastructural and morphological criteria indicate that the described species belongs to the genus Pleistophora.

Cryptochlorophyllous Spores in Ferns: Nongreen Spores that Contain Chlorophyll

In terms of color, fern spores have traditionally been classified as either green or nongreen. This study reports a new kind of spore, here termed “cryptochlorophyllous.” Such spores contain chlorophyll but do not appear green when examined with either the naked eye or a light microscope. Epifluorescence microscopy was used to detect chlorophyll in cryptochlorophyllous spores. To test one aspect of the reliability of this method, we examined whether chlorophyll degradation over time would give false negative results. We found that in two species with green spores (Osmundastrum cinnamomeum and Terpsichore asplenifolia), fluorescence weakened with but could still be detected in specimens that were 110 yr old. We surveyed the spores of species in three fern genera under white light and with epifluorescence microscopy. Under white light, green spores were seen in 10 (26%) of 39 species of Elaphoglossum, two (17%) of 12 species of Lomariopsis, and seven (25%) of 28 species of Pleopeltis. When spores from the s...

Combined LM and SEM study of the Middle Miocene (Sarmatian) palynoflora from the Lavanttal Basin, Austria: Part I. Bryophyta, Lycopodiophyta, Pteridophyta, Ginkgophyta, and Gnetophyta

Preliminary studies of the palynoflora from the Lavanttal Basin show a relatively rich assemblage of pollen and spores. The palynoflora comprises at least 17 different kinds of spores, representing the Bryophyta (Sphagnum), Lycopodiophyta (Lycopodium, Selaginella), and the Pteridophyta (Dryopteris, Osmunda, Pteris), about 20 different pollen types of conifers assignable to Cupressaceae and Pinaceae, and 130–160 different kinds of angiosperm pollen. In this study, we describe all spores together with pollen from two seed plants, i.e. Ginkgo (Ginkgophyta) and Ephedra (Gnetophyta). The fossil spores and pollen grains are preserved in phosphoritic nodules. Absence of palynomorphs characteristic of marine settings and presence of numerous freshwater algae (diatoms, dinoflagellates, and different green algae) indicate freshwater environments. This is also supported by sedimentological observations suggestive of wetland surroundings, characterised by lakes, swamps, streams, rivers and floodplain areas. The taxa reported here all seem to represent part of azonal vegetation with plants growing in swamps, on hummocks, along border of lakes or streams, on levees, or on sandy patches of floodplains. Preliminary results suggest that the vegetation thrived under a relatively warm and humid climate.

Unresolved problems on the origin and early evolution of land plants.

The origin of land plants or embryophytes from the Charophyceae is generally accepted today by the botanists. In fact, numerous morphological, cytological, ultrastructural, biochemical and molecular characters are shared in these organisms. A fundamental problem is still constituted by the evolution of the sporophyte, i.e. the appearance of two different phase cycles (gametophyte/sporophyte alternance), although two theories ("antithetic" and "homologous") try to explain this evolutionary event.However, another phylogenetic dilemma is represented, in my opinion, either by the formation of bryophytes or by the transition from these first land plants to the pteridophytes, considering them at whole organism level. The bryophyte gametophyte is the most elaborate of the land plants. It presents several complex characters, principally the growth developmental form, the appearance of multicellular sex organs, antheridia and archegonia. Also the sporophyte shows a complicated structure that is not found in the other land plants or tracheophytes. The sporangium, in particular, exhibits some intricate morphological traits such as the peristome of true mosses for spore dispersion, the elaters of liverworts and the indeterminate growth in the hornworts. The pteridophytes are represented especially by their dominant sporophyte. This latter has the capacity to produce multiple sporangia and, in many cases, two kinds of spores which develop in male and female gametophyte (heterosporous pteridophytes). Another important characteristic of this sporophyte is its ability to become independent of the gametophyte. However, one of the most innovative character is the formation of true vascular elements (xylem and phloem). All these very large evolutionary jumps are discussed on the basis of the phyletic gradualistic neo-Darwinian theory and the punctuated equilibrium theory of Eldredge and Gould. In this context other genetic evolutionary mechanisms are also considered.Nevertheless, the origin of bryophytes and pteridophytes remain, at the moment, a mystery.

REN1 is required for development of microconidia and macroconidia, but not of chlamydospores, in the plant pathogenic fungus Fusarium oxysporum.

The filamentous fungus Fusarium oxysporum is a soil-borne facultative parasite that causes economically important losses in a wide variety of crops. F. oxysporum exhibits filamentous growth on agar media and undergoes asexual development producing three kinds of spores: microconidia, macroconidia, and chlamydospores. Ellipsoidal microconidia and falcate macroconidia are formed from phialides by basipetal division; globose chlamydospores with thick walls are formed acrogenously from hyphae or by the modification of hyphal cells. Here we describe rensa, a conidiation mutant of F. oxysporum, obtained by restriction-enzyme-mediated integration mutagenesis. Molecular analysis of rensa identified the affected gene, REN1, which encodes a protein with similarity to MedA of Aspergillus nidulans and Acr1 of Magnaporthe grisea. MedA and Acr1 are presumed transcription regulators involved in conidiogenesis in these fungi. The rensa mutant and REN1-targeted strains lack normal conidiophores and phialides and form rod-shaped, conidium-like cells directly from hyphae by acropetal division. These mutants, however, exhibit normal vegetative growth and chlamydospore formation. Nuclear localization of Ren1 was verified using strains expressing the Ren1-green fluorescent protein fusions. These data strongly suggest that REN1 encodes a transcription regulator required for the correct differentiation of conidiogenesis cells for development of microconidia and macroconidia in F. oxysporum.

Pathology and morphology of Ichthyophonus hoferi in naturally infected fishes off the Swedish west coast.

The pathology and morphology of Ichthyophonus hoferi was studied in naturally infected Atlantic herring Clupea harengus, in sprat Sprattus sprattus, and in flounder Pleuronectes flesus from the west coast of Sweden. The pathogen was found in all organs examined, with the intensity of infection varying in different organs of the different fish species. Two main phases in the life of infecting parasites were identified, 'active' and 'passive', the latter being able to switch to active. The active phase of the infection in herring was usually accompanied by a lean and slender appearance of the body, a drastic decrease in intestinal fat, emaciation of the somatic muscles, swelling of the visceral organs, poor quality of flesh texture and a distinctive off-odour. The most characteristic macroscopic sign of ichthyophonosis in herring and flounder was the occurrence of creamy white nodules on the heart. The infection causes a chronic systemic granulomatous inflammation. The nature of the granulomatous inflammation was host- and tissue-dependent. The pathogenicity of the parasite in its active form and the side effects of host defence cells were also reflected in dramatic tissue damage and loss of structure and function of the infected organs. Three kinds of spores were identified: 'un-developing spore', 'developing spore' and 'plasmodio-spore'. The formation and spread of 'plasmodia', from plasmodio-spores, as a secondary infection agent is documented. Transmission electron microscopy revealed I. hoferi to be multinucleated, containing different organelles and structures. These included a cell wall, an undulating cell membrane, a thin paramural endoplasm, an endoplasmic reticulum, polymorphic but usually spherical mitochondria with short tubulo-vesicular cristae, dictyosomes with plate-like cristernae, large electron-dense lipid droplets and electron-lucid vacuoles, probably containing glycogen.

The basidium of Tilletia and its evolution

An historical account is given of the basidium in Tilletia . Its basidiospores, and the kinds of spore resulting directly or indirectly from their germination, are considered and compared. It is suggested that the filamentous basidiospores of Tilletia and the blastospores, formed on the mycelium resulting from their germination, represent degenerate ballistospores, a view supported by a consideration of Ingoldiomyces hyalosporus in which the basidiospores are ballistospores. The situation in Tilletia spp. is compared with that in Urocystis violae the basidiospores of which, though readily set free into the air, are not ballistospores.

Characteristics of spores formed by surface and submerged cultures of Streptomyces albidoflavus SMF301

SUMMARY: Streptomyces albidoflavus SMF301 produced abundant spores in submerged cultures (submerged spores) as well as on solid media (aerial spores). The content of carbon, hydrogen, nitrogen, and phosphorus in submerged and aerial spores was similar; however, the contents of metal ions (K+, Na+, Ca2+ and Mg2+) were very different. Glutamic acid, alanine, and glycine, all known to be cell-wall components, were the major amino acids in both types of spores. However, cysteine was more abundant in submerged spores than in aerial spores. The major fatty acid in aerial spores was n-C18 (61.74%), whereas in submerged spores it was ai-C16 (33.68%). The contents of ai-C14, and ai-C17 in submerged spores were also very much higher than in aerial spores. Unsaturated fatty acids were found in both kinds of spores but not in mycelium; they were particularly abundant in submerged spores. The composition of menaquinones in the two kinds of spores also varied. The resistance of aerial spores to lysozyme digestion, mild acid treatment, heating and desiccation was higher than that of submerged spores, but the submerged spores were more resistant to sonication.

Differences in Dispersal Abilities of Haploid and Diploid Spores of Gracilaria verrucosa (Gracilariales, Rhodophyta)

In some red algae, the establishment of new fixed individuals is due to two kinds of spores : haploid spores producing gametophytes and diploid spores producing sporophytes. Spore dispersal abilities were studied in order to understand setlement patterns in algal populations. Spore dispersal depends principally on their survival and how long they remain viable whilst suspended in the water column. It has been suggested that there is a positive correlation between spore size and their sedimentation rate. In Gracilaria verrucosa haploid spores are smaller than diploid ones. Nevertheless when submitted to a slow controlled water current, spore size had no effect their dispersal. Conversely, under different light conditions, haploid spores have a better survival and remain free-floating longer than diploid ones; thus haploid spores could have better dispersal abilities than diploid ones

Some characteristics of aerial and submerged spores of Kitasatosporia setalba.

Kitasatosporia setalba KM-6054 forms two kinds of spores: aerial spores on an agar medium and submerged spores in a liquid medium. In this study, both kinds of spores were resistant to sonication, but sensitive to lysozyme digestion and moist heat. LL-2, 6-Diaminopimelic acid (A2pm), alanine, glutamic acid and glycine were detected as the main constituents in the cell walls of the aerial and submerged spores. The respective molar ratios were similar; 1.0:1.6:0.5:1.0 and 1.0:1.5:0.7:0.8. On the other hand, the vegetative mycelium on agar media and the filamentous mycelium in submerged cultures were sensitive to sonication and differed from the two kinds of spores in both amino acid composition and A2pm type.