Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 7 de 7
Filter
Add more filters










Database
Language
Publication year range
1.
Fungal Biol ; 122(6): 457-464, 2018 06.
Article in English | MEDLINE | ID: mdl-29801789

ABSTRACT

The entomopathogenic fungus Beauveria bassiana is able to grow on insect cuticle hydrocarbons, inducing alkane assimilation pathways and concomitantly increasing virulence against insect hosts. In this study, we describe some physiological and molecular processes implicated in growth, nutritional stress response, and cellular alterations found in alkane-grown fungi. The fungal cytology was investigated using light and transmission electron microscopy while the surface topography was examined using atomic force microscopy. Additionally, the expression pattern of several genes associated with oxidative stress, peroxisome biogenesis, and hydrophobicity were analysed by qPCR. We found a novel type of growth in alkane-cultured B. bassiana similar to mycelial pellets described in other alkane-free fungi, which were able to produce viable conidia and to be pathogenic against larvae of the beetles Tenebrio molitor and Tribolium castaneum. Mycelial pellets were formed by hyphae cumulates with high peroxidase activity, exhibiting peroxisome proliferation and an apparent surface thickening. Alkane-grown conidia appeared to be more hydrophobic and cell surfaces displayed different topography than glucose-grown cells. We also found a significant induction in several genes encoding for peroxins, catalases, superoxide dismutases, and hydrophobins. These results show that both morphological and metabolic changes are triggered in mycelial pellets derived from alkane-grown B. bassiana.


Subject(s)
Alkanes/metabolism , Beauveria/growth & development , Beauveria/pathogenicity , Entomophthorales/growth & development , Entomophthorales/pathogenicity , Oxidative Stress , Animals , Beauveria/metabolism , Cell Membrane/ultrastructure , Cell Proliferation , Entomophthorales/metabolism , Hyphae/metabolism , Insecta/microbiology , Larva/microbiology , Peroxisomes/physiology , Spores, Fungal/metabolism , Virulence
2.
Fungal Biol ; 122(6): 538-545, 2018 06.
Article in English | MEDLINE | ID: mdl-29801798

ABSTRACT

Entomopathogenic fungi of the order Hypocreales infect their insect hosts mainly by penetrating through the cuticle and colonize them by proliferating throughout the body cavity. In order to ensure a successful infection, fungi first produce a variety of degrading enzymes that help to breach the insect cuticle, and then secrete toxic secondary metabolites that facilitate fungal invasion of the hemolymph. In response, insect hosts activate their innate immune system by triggering both cellular and humoral immune reactions. As fungi are exposed to stress in both cuticle and hemolymph, several mechanisms are activated not only to deal with this situation but also to mimic host epitopes and evade the insect's immune response. In this review, several components involved in the molecular interaction between insects and fungal pathogens are described including chemical, metabolomics, and dual transcriptomics approaches; with emphasis in the involvement of cuticle surface components in (pre-) infection processes, and fungal secondary metabolite (non-ribosomally synthesized peptides and polyketides) analysis. Some of the mechanisms involved in such interaction are also discussed.


Subject(s)
Beauveria/metabolism , Entomophthorales/metabolism , Host-Pathogen Interactions/immunology , Hypocreales/metabolism , Insecta/metabolism , Metarhizium/metabolism , Secondary Metabolism , Animals , Beauveria/genetics , Beauveria/immunology , Beauveria/pathogenicity , Biological Coevolution , Entomophthorales/genetics , Entomophthorales/immunology , Entomophthorales/pathogenicity , Hemolymph , Hypocreales/genetics , Hypocreales/immunology , Hypocreales/pathogenicity , Insecta/genetics , Insecta/immunology , Insecta/microbiology , Metarhizium/genetics , Metarhizium/immunology , Metarhizium/pathogenicity , Sequence Analysis, RNA/methods
3.
Appl Microbiol Biotechnol ; 100(7): 3301-11, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26637423

ABSTRACT

Biofilm formation in drinking water distribution systems (DWDS) is influenced by the source water, the supply infrastructure and the operation of the system. A holistic approach was used to advance knowledge on the development of mixed species biofilms in situ, by using biofilm sampling devices installed in chlorinated networks. Key physico-chemical parameters and conventional microbial indicators for drinking water quality were analysed. Biofilm coverage on pipes was evaluated by scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM). The microbial community structure, bacteria and fungi, of water and biofilms was assessed using pyrosequencing. Conventional wisdom leads to an expectation for less microbial diversity in groundwater supplied systems. However, the analysis of bulk water showed higher microbial diversity in groundwater site samples compared with the surface water site. Conversely, higher diversity and richness were detected in biofilms from the surface water site. The average biofilm coverage was similar among sites. Disinfection residual and other key variables were similar between the two sites, other than nitrates, alkalinity and the hydraulic conditions which were extremely low at the groundwater site. Thus, the unexpected result of an exceptionally low diversity with few dominant genera (Pseudomonas and Basidiobolus) in groundwater biofilm samples, despite the more diverse community in the bulk water, is attributed to the low-flow hydraulic conditions. This finding evidences that the local environmental conditions are shaping biofilm formation, composition and amount, and hence managing these is critical for the best operation of DWDS to safeguard water quality.


Subject(s)
Biofilms/growth & development , Drinking Water/microbiology , Entomophthorales/genetics , Pseudomonas/genetics , Water Microbiology , Water Quality , Alkalies/chemistry , Biodiversity , Entomophthorales/growth & development , Entomophthorales/metabolism , Halogenation , High-Throughput Nucleotide Sequencing , Humans , Microbial Consortia/genetics , Nitrates/chemistry , Pseudomonas/growth & development , Pseudomonas/metabolism , Water Supply
4.
J Basic Microbiol ; 52(5): 539-48, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22359366

ABSTRACT

The influence of concentration of medium components such as colloidal chitin, lactose, malt extract, yeast extract, and peptone on the chitinase production from Basidiobolous ranarum at the flask level were studied by using statistical tool Central Composite Design (CCD) and analysed by Response Surface Methodology (RSM). The results revealed that colloidal chitin, malt extract and peptone had significant effect (P < 0.01) on the chitinase production at their individual levels. The polynomial equation of the model developed incorporates 3 linear, 3 quadratic and 5 interactive terms. Maximum chitinase production of 3.47 U ml(-1) was achieved with 1.5% colloidal chitin, 0.125% lactose, 0.025% malt extract and 0.075% peptone. After optimization, chitinase activity was increased by 7.71 fold. A second order polynomial equation was found to be useful for the development of efficient bioprocess for chitinase production. To screen the biotechnological potential of this enzyme, degradation of fungal mycelia by ammonium sulphate precipitate of the same was studied for several pathogenic fungi-in vitro which showed promising results particularly against Rhizoctonia solani and Fusarium solani. This study provides the first evidence showing the effectiveness of RSM for the development of a robust statistical model for the chitinase production by Basidiobolus and for its application in the biocontrol of phytopathogenic fungi.


Subject(s)
Antifungal Agents/metabolism , Antifungal Agents/pharmacology , Chitinases/metabolism , Chitinases/pharmacology , Entomophthorales/growth & development , Entomophthorales/metabolism , Culture Media/chemistry , Fusarium/drug effects , Mycelium/drug effects , Rhizoctonia/drug effects
5.
Clin Microbiol Infect ; 15 Suppl 5: 26-32, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19754753

ABSTRACT

Iron is an essential element for cell growth and development, contributing to DNA synthesis and regulating the G(1)-phase to S-phase transition. Moreover, iron is important for the virulence of the majority of microorganisms, and the function of the genes regulating iron uptake is coupled with the manifestations of the virulence phenotype. All fungi elaborate specific uptake mechanisms to sequester iron, and most commonly produce small molecules with high affinity for iron, the siderophores. The importance of iron appears to be particularly high for Zygomycetes, which grow abundantly in iron-rich media, and all the known predisposing factors for zygomycosis have, as a common feature, the increased availability of free iron. Among the known iron chelators, deferoxamine supports the growth of Zygomycetes because it acts as xenosiderophore, delivering iron to iron-uptaking molecules of these species. Conversely, the newer iron chelators deferiprone and deferasirox do not exhibit similar activity, apparently because they share higher affinity constants for iron and, as a result, deprive the fungi of iron, inhibiting their growth. This activity has been documented in various culture systems and in many animal models of zygomycosis, and therefore suggests that these drugs might be used as adjuvant treatment for systemic zygomycosis. There are few case reports in which the newer iron chelators have been used as antifungals, and their possible benefit must be verified in a prospective randomized trial.


Subject(s)
Antifungal Agents/metabolism , Chelating Agents/metabolism , Entomophthorales/metabolism , Iron/metabolism , Mucorales/metabolism , Zygomycosis/microbiology , Antifungal Agents/therapeutic use , Chelating Agents/therapeutic use , Entomophthorales/pathogenicity , Mucorales/pathogenicity , Virulence , Zygomycosis/drug therapy
6.
Mycol Res ; 111(Pt 12): 1437-49, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18035528

ABSTRACT

This study of the putative saprotrophs of Conidiobolus and Basidiobolus aids the understanding of their ecological roles in litter, and their relationship with the entomogenous fungi of the Entomophthorales. A total of 47 isolates (ten spp.) were screened for their ability to utilise pure compounds, arthropod cadavers, and plant leaf fragments as substrates. Isolates co-occurred in a larch plantation (Larix sp.) or were from adjacent habitats. Of the 21 isolates (nine spp.) tested on potential prime carbon sources, none could utilise common plant structural polymers. Conidiobolus adiaeretus, C. iuxtagenitus, and B. ranarum from litter and some soil isolates of C. heterosporus, C. pumilus, and C. firmipilleus could use starches and glycogen. In marked contrast, all could utilise animal chitin, gelatine, casein, N-acetyl glucosamine, and trehalose. The lipids tributyrin and sunflower oil also supported growth. Conidia on cadavers usually led to high levels of colonisation as was the case for 30 isolates (ten species). Collembola were more frequently and rapidly colonised than mites. Cadavers of many other arthropods were also internally colonised. The ability to utilise cadavers of diverse arthropods indicates that trophic competition between co-occurring test species may be minimal. Niche differentiation may depend more on non-trophic features of their life history. Negative correlation of performance with the presence of naturally occurring, non-test fungi suggests competition with (or antibiosis from) at least some of the other fungi. In washed or unwashed plant fragments of larch litter (F-layer) only occasional local growth and resting spore formation occurred. Extra nutrients did not facilitate colonisation. Alternative forms of repetitional conidia showed a strong association with plant fragments but not with cadavers.


Subject(s)
Biodegradation, Environmental , Conidiobolus/metabolism , Ecosystem , Entomophthorales/metabolism , Larix , Plant Leaves/metabolism , Animals , Arthropods/metabolism , Cadaver , Carbon/metabolism , Spores, Fungal
7.
Folia Microbiol (Praha) ; 44(4): 397-400, 1999.
Article in English | MEDLINE | ID: mdl-10983235

ABSTRACT

Primary cell wall is synthesized in the growth zone of hyphal apex in fungi and rigidified during maturation along the newly formed hypha. Cross-linking of cell-wall components and self-assembly of individual polysaccharide chains into microfibrils are supposed to be involved in the rigidification process. We determined the relative chitin content in the cell wall of hyphal tips and distal walls of three fungal species and demonstrated a general increase in relative chitin content in mature cell walls. Thus, this increase can be supposed to raise cell-wall rigidity as the principal role of chitin in the determination of cell-wall rigidity is beyond doubt.


Subject(s)
Chitin/metabolism , Coprinus/metabolism , Entomophthorales/metabolism , Neurospora crassa/metabolism , Cell Wall/metabolism , Coprinus/growth & development , Entomophthorales/growth & development , Neurospora crassa/growth & development , Species Specificity
SELECTION OF CITATIONS
SEARCH DETAIL
...