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1.
Mol Phylogenet Evol ; 197: 108103, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38754710

ABSTRACT

Parasitism is the most common lifestyle on Earth and has emerged many times independently across the eukaryotic tree of life. It is frequently found among chytrids (Chytridiomycota), which are early-branching unicellular fungi that feed osmotrophically via rhizoids as saprotrophs or parasites. Chytrids are abundant in most aquatic and terrestrial environments and fulfil important ecosystem functions. As parasites, they can have significant impacts on host populations. They cause global amphibian declines and influence the Earth's carbon cycle by terminating algal blooms. To date, the evolution of parasitism within the chytrid phylum remains unclear due to the low phylogenetic resolution of rRNA genes for the early diversification of fungi, and because few parasitic lineages have been cultured and genomic data for parasites is scarce. Here, we combine transcriptomics, culture-independent single-cell genomics and a phylogenomic approach to overcome these limitations. We newly sequenced 29 parasitic taxa and combined these with existing data to provide a robust backbone topology for the diversification of Chytridiomycota. Our analyses reveal multiple independent lifestyle transitions between parasitism and saprotrophy among chytrids and multiple host shifts by parasites. Based on these results and the parasitic lifestyle of other early-branching holomycotan lineages, we hypothesise that the chytrid last common ancestor was a parasite of phytoplankton.


Subject(s)
Chytridiomycota , Phylogeny , Phytoplankton , Chytridiomycota/genetics , Chytridiomycota/classification , Phytoplankton/genetics , Phytoplankton/classification , Genomics
2.
Mol Plant Microbe Interact ; 32(11): 1536-1546, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31246152

ABSTRACT

Synchytrium endobioticum is an obligate biotrophic fungus of division Chytridiomycota. It causes potato wart disease, has a worldwide quarantine status and is included on the Health and Human Services and United States Department of Agriculture Select Agent list. S. endobioticum isolates are grouped in pathotypes based on their ability to evade host resistance in a set of differential potato varieties. Thus far, 39 pathotypes are reported. A single dominant gene (Sen1) governs pathotype 1 (D1) resistance and we anticipated that the underlying molecular model would involve a pathogen effector (AvrSen1) that is recognized by the host. The S. endobioticum-specific secretome of 14 isolates representing six different pathotypes was screened for effectors specifically present in pathotype 1 (D1) isolates but absent in others. We identified a single AvrSen1 candidate. Expression of this candidate in potato Sen1 plants showed a specific hypersensitive response (HR), which cosegregated with the Sen1 resistance in potato populations. No HR was obtained with truncated genes found in pathotypes that evaded recognition by Sen1. These findings established that our candidate gene was indeed Avrsen1. The S. endobioticum AvrSen1 is a single-copy gene and encodes a 376-amino-acid protein without predicted function or functional domains, and is the first effector gene identified in Chytridiomycota, an extremely diverse yet underrepresented basal lineage of fungi.


Subject(s)
Chytridiomycota , Genes, Fungal , Solanum tuberosum , Chytridiomycota/classification , Chytridiomycota/genetics , Chytridiomycota/immunology , Genes, Fungal/immunology , Plant Diseases/immunology , Plant Diseases/microbiology , Solanum tuberosum/immunology , Solanum tuberosum/microbiology
3.
Emerg Infect Dis ; 25(7): 1416-1418, 2019 07.
Article in English | MEDLINE | ID: mdl-31211934

ABSTRACT

The distribution of the chytrid fungus Batrachochytrium salamandrivorans continues to expand in Europe. During 2014-2018, we collected 1,135 samples from salamanders and newts in 6 countries in Europe. We identified 5 cases of B. salamandrivorans in a wild population in Spain but none in central Europe or the Balkan Peninsula.


Subject(s)
Animal Diseases/microbiology , Chytridiomycota , Mycoses/veterinary , Urodela/microbiology , Animal Diseases/diagnosis , Animals , Chytridiomycota/classification , Chytridiomycota/genetics , Chytridiomycota/isolation & purification , Polymerase Chain Reaction
4.
J Eukaryot Microbiol ; 66(4): 582-591, 2019 07.
Article in English | MEDLINE | ID: mdl-30460733

ABSTRACT

Molecular phylogenetic analysis of 18S rRNA gene sequences of nearly any species of Chytridiomycota has typically challenged traditional classification and triggered taxonomic revision. This has often led to the establishment of new taxa which, normally, appears well supported by zoospore ultrastructure, which provides diagnostic characters. To construct a meaningful and comprehensive classification of Chytridiomycota, the combination of molecular phylogenies and morphological studies of traditionally defined chytrid species is needed. In this work, we have studied morphological and ultrastructural features based on light and transmission electron microscopy as well as molecular phylogenetic analysis of a parasite (strain X-124 CCPP ZIN RAS) morphologically similar to Rhizophydium granulosporum living on the yellow-green alga Tribonema gayanum. Phylogenetic analysis of the 18S rRNA gene sequence of this strain supports that it represents a new genus and species affiliated to the recently established order Gromochytriales. The ultrastructure of X-124 confirms its phylogenetic position sister to Gromochytrium and serves as the basis for the description of the new genus and species Apiochytrium granulosporum. The 18S rRNA gene of A. granulosporum contains a S943 group I intron that carries a homing endonuclease pseudogene.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/genetics , Chytridiomycota/ultrastructure , Microscopy , Microscopy, Electron, Transmission , Phylogeny , RNA, Fungal/analysis , RNA, Ribosomal, 18S/analysis
5.
Appl Environ Microbiol ; 84(23)2018 12 01.
Article in English | MEDLINE | ID: mdl-30266725

ABSTRACT

Parasitic Chytridiomycota (chytrids) are ecologically significant in various aquatic ecosystems, notably through their roles in controlling bloom-forming phytoplankton populations and in facilitating the transfer of nutrients from inedible algae to higher trophic levels. The diversity and study of these obligate parasites, while critical to understand the interactions between pathogens and their hosts in the environment, have been hindered by challenges inherent to their isolation and stable long-term maintenance under laboratory conditions. Here, we isolated an obligate chytrid parasite (CCAP 4086/1) on the freshwater bloom-forming diatom Asterionella formosa and characterized its infectious cycle under controlled conditions. Phylogenetic analyses based on 18S, 5.8S, and 28S ribosomal DNAs (rDNAs) revealed that this strain belongs to the recently described clade SW-I within the Lobulomycetales. All morphological features observed agree with the description of the known Asterionella parasite Zygorhizidium affluens Canter. We thus provide a phylogenetic placement for this chytrid and present a robust and simple assay that assesses both the infection success and the viability of the host. We also validate a cryopreservation method for stable and cost-effective long-term storage and demonstrate its recovery after thawing. All the above-mentioned tools establish a new gold standard for the isolation and long-term preservation of parasitic aquatic chytrids, thus opening new perspectives to investigate the diversity of these organisms and their physiology in a controlled laboratory environment.IMPORTANCE Despite their ecological relevance, parasitic aquatic chytrids are understudied, especially due to the challenges associated with their isolation and maintenance in culture. Here we isolated and established a culture of a chytrid parasite infecting the bloom-forming freshwater diatom Asterionella formosa The chytrid morphology suggests that it corresponds to the Asterionella parasite known as Zygorhizidium affluens The phylogenetic reconstruction in the present study supports the hypothesis that our Z. affluens isolate belongs to the order Lobulomycetales and clusters within the novel clade SW-I. We also validate a cryopreservation method for stable and cost-effective long-term storage of parasitic chytrids of phytoplankton. The establishment of a monoclonal pathosystem in culture and its successful cryopreservation opens the way to further investigate this ecologically relevant parasitic interaction.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Cryopreservation/methods , Diatoms/microbiology , Chytridiomycota/genetics , Chytridiomycota/pathogenicity , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Phylogeny , RNA, Ribosomal, 28S/genetics , Taiwan , Virulence
6.
J Eukaryot Microbiol ; 65(6): 870-881, 2018 11.
Article in English | MEDLINE | ID: mdl-29752884

ABSTRACT

Chytrids are zoosporic fungi that play an important, but yet understudied, ecological role in aquatic ecosystems. Many chytrid species have been morphologically described as parasites on phytoplankton. However, the majority of them have rarely been isolated and lack DNA sequence data. In this study we isolated and cultivated three parasitic chytrids, infecting a common volvocacean host species, Yamagishiella unicocca. To identify the chytrids, we characterized morphology and life cycle, and analyzed phylogenetic relationships based on 18S and 28S rDNA genes. Host range and specificity of the chytrids was determined by cross-infection assays with host strains, characterized by rbcL and ITS markers. We were able to confirm the identity of two chytrid strains as Endocoenobium eudorinae Ingold and Dangeardia mamillata Schröder and described the third chytrid strain as Algomyces stechlinensis gen. et sp. nov. The three chytrids were assigned to novel and phylogenetically distant clades within the phylum Chytridiomycota, each exhibiting different host specificities. By integrating morphological and molecular data of both the parasitic chytrids and their respective host species, we unveiled cryptic host-parasite associations. This study highlights that a high prevalence of (pseudo)cryptic diversity requires molecular characterization of both phytoplankton host and parasitic chytrid to accurately identify and compare host range and specificity, and to study phytoplankton-chytrid interactions in general.


Subject(s)
Chlorophyceae/microbiology , Chytridiomycota/classification , Chytridiomycota/isolation & purification , Chytridiomycota/pathogenicity , Host Specificity , Phylogeny , Chytridiomycota/genetics , Cross Infection , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Germany , Host-Parasite Interactions , Lakes/microbiology , Life Cycle Stages , Phytoplankton/microbiology , RNA, Ribosomal, 18S/genetics , RNA, Ribosomal, 28S/genetics
7.
Microb Ecol ; 75(2): 505-514, 2018 Feb.
Article in English | MEDLINE | ID: mdl-28725944

ABSTRACT

In organisms with complex life histories, dramatic changes in microbial community structure may occur with host development and immune system maturation. Amphibian host susceptibility to diseases such as chytridiomycosis may be affected by the reorganization of skin microbial community structure that occurs during metamorphosis. We tracked changes in the bacterial communities inhabiting skin of Korean fire-bellied toads (Bombina orientalis) that we infected as tadpoles with different strains of Batrachochytrium dendrobatidis (Bd), the pathogenic fungus that causes chytridiomycosis. We found that B. orientalis undergoes a major change in skin bacterial community composition between 5 and 15 days following metamorphosis. Richness indices and phylogenetic diversity measures began to diverge earlier, between aquatic and terrestrial stages. Our results further reveal differences in skin bacterial community composition among infection groups, suggesting that the effect of Bd infection on skin microbiome composition may differ by Bd strain. Additional studies are needed to further investigate the structural and temporal dynamics of microbiome shifts during metamorphosis in wild and captive amphibian populations. Analyses of the ontogeny of microbiome shifts may contribute to an understanding of why amphibians vary in their susceptibility to chytridiomycosis.


Subject(s)
Anura/growth & development , Anura/microbiology , Bacteria/isolation & purification , Microbiota , Skin/microbiology , Animals , Bacteria/classification , Bacteria/genetics , Chytridiomycota/classification , Chytridiomycota/genetics , Chytridiomycota/isolation & purification , Metamorphosis, Biological , Mycoses/microbiology , Mycoses/veterinary , Phylogeny
8.
Environ Microbiol ; 19(10): 3802-3822, 2017 10.
Article in English | MEDLINE | ID: mdl-28618196

ABSTRACT

Chytridiomycota, often referred to as chytrids, can be virulent parasites with the potential to inflict mass mortalities on hosts, causing e.g. changes in phytoplankton size distributions and succession, and the delay or suppression of bloom events. Molecular environmental surveys have revealed an unexpectedly large diversity of chytrids across a wide range of aquatic ecosystems worldwide. As a result, scientific interest towards fungal parasites of phytoplankton has been gaining momentum in the past few years. Yet, we still know little about the ecology of chytrids, their life cycles, phylogeny, host specificity and range. Information on the contribution of chytrids to trophic interactions, as well as co-evolutionary feedbacks of fungal parasitism on host populations is also limited. This paper synthesizes ideas stressing the multifaceted biological relevance of phytoplankton chytridiomycosis, resulting from discussions among an international team of chytrid researchers. It presents our view on the most pressing research needs for promoting the integration of chytrid fungi into aquatic ecology.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/pathogenicity , Mycoses/microbiology , Phytoplankton/microbiology , Animals , Biological Evolution , Ecology , Ecosystem , Environmental Microbiology , Food Chain , Host Specificity , Phylogeny
9.
Environ Microbiol ; 19(11): 4447-4459, 2017 11.
Article in English | MEDLINE | ID: mdl-28805294

ABSTRACT

Despite increasing concerns about microplastic (MP) pollution in aquatic ecosystems, there is insufficient knowledge on how MP affect fungal communities. In this study, we explored the diversity and community composition of fungi attached to polyethylene (PE) and polystyrene (PS) particles incubated in different aquatic systems in north-east Germany: the Baltic Sea, the River Warnow and a wastewater treatment plant. Based on next generation 18S rRNA gene sequencing, 347 different operational taxonomic units assigned to 81 fungal taxa were identified on PE and PS. The MP-associated communities were distinct from fungal communities in the surrounding water and on the natural substrate wood. They also differed significantly among sampling locations, pointing towards a substrate and location specific fungal colonization. Members of Chytridiomycota, Cryptomycota and Ascomycota dominated the fungal assemblages, suggesting that both parasitic and saprophytic fungi thrive in MP biofilms. Thus, considering the worldwide increasing accumulation of plastic particles as well as the substantial vector potential of MP, especially these fungal taxa might benefit from MP pollution in the aquatic environment with yet unknown impacts on their worldwide distribution, as well as biodiversity and food web dynamics at large.


Subject(s)
Ascomycota/drug effects , Chytridiomycota/drug effects , Polyethylene/pharmacology , Polystyrenes/pharmacology , Water Pollutants, Chemical/pharmacology , Ascomycota/classification , Ascomycota/growth & development , Biodiversity , Chytridiomycota/classification , Chytridiomycota/growth & development , Ecosystem , RNA, Ribosomal, 18S/genetics , Rivers/chemistry , Wastewater/chemistry , Water Pollutants, Chemical/chemistry , Water Pollution, Chemical
10.
J Eukaryot Microbiol ; 64(3): 383-393, 2017 05.
Article in English | MEDLINE | ID: mdl-27714973

ABSTRACT

Chytrids are true fungi that reproduce with posteriorly uniflagellate zoospores. In the last decade, environmental DNA surveys revealed a large number of uncultured chytrids as well as undescribed order-level novel clades in Chytridiomycota. Although many species have been morphologically described, only some DNA sequence data of parasitic chytrids are available from the database. We herein discuss five cultures of parasitic chytrids on diatoms Aulacoseira spp. and Asterionella formosa. In order to identify the chytrids examined, thallus morphologies were observed using light microscopy. We also conducted a phylogenetic analysis using 18S, 5.8S, and 28S rDNA sequences to obtain their phylogenetic positions. Based on their morphological characteristics, two cultures parasitic on As. formosa were identified as Rhizophydium planktonicum and Zygorhizidium planktonicum. The other three cultures infecting Aulacoseira spp. (two on Aulacoseira ambigua and the other on Aulacoseira granulata) were regarded as Zygorhizidium aff. melosirae. The results of the molecular phylogenetic analysis revealed that R. planktonicum belonged to the known order Chytridiales, while the two species of Zygorhizidium were placed in a novel clade that was previously reported as an undescribed clade composed of only the environmental sequences of uncultured chytrids.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Diatoms/parasitology , Fungi/classification , Fungi/isolation & purification , Phylogeny , Base Sequence , Chytridiomycota/cytology , Chytridiomycota/genetics , Classification , DNA, Fungal/genetics , DNA, Fungal/isolation & purification , DNA, Ribosomal/genetics , Fungi/cytology , Fungi/genetics , Japan , Microscopy , RNA, Ribosomal, 28S/genetics , RNA, Ribosomal, 5.8S/genetics , Species Specificity , Taiwan
11.
J Phycol ; 53(3): 720-724, 2017 06.
Article in English | MEDLINE | ID: mdl-28295358

ABSTRACT

Unusual microfossils that occurred associated with fungal spores in the Lower Devonian (~410 mya) Windyfield chert from Scotland were composed of a narrow stipe (2.5-9 µm long) to which was attached an obovoid or elongate drop-shaped cell up to 14 µm long; a basal attachment pad was present in several specimens. The fossils were strikingly similar morphologically to certain present-day unicellular freshwater Tribophyceae and Chlorophyceae, but affinities to the fungal phylum Chytridiomycota also cannot be ruled out. This discovery adds to the inventory of distinctive microbial morphologies in the early non-marine paleoecosystems.


Subject(s)
Chlorophyta/classification , Chytridiomycota/classification , Fossils , Microalgae/classification , Stramenopiles/classification , Chlorophyta/cytology , Chytridiomycota/cytology , Microalgae/cytology , Scotland , Stramenopiles/cytology
12.
Microb Ecol ; 72(1): 197-206, 2016 07.
Article in English | MEDLINE | ID: mdl-26992401

ABSTRACT

Tall fescue (Schedonorus arundinaceus) is a widespread grass that can form a symbiotic relationship with a shoot-specific fungal endophyte (Epichloë coenophiala). While the effects of fungal endophyte infection on fescue physiology and ecology have been relatively well studied, less attention has been given to how this relationship may impact the soil microbial community. We used high-throughput DNA sequencing and phospholipid fatty acid analysis to determine the structure and biomass of microbial communities in both bulk and rhizosphere soils from tall fescue stands that were either uninfected with E. coenophiala or were infected with the common toxic strain or one of several novel strains of the endophyte. We found that rhizosphere and bulk soils harbored distinct microbial communities. Endophyte presence, regardless of strain, significantly influenced soil fungal communities, but endophyte effects were less pronounced in prokaryotic communities. E. coenophiala presence did not change total fungal biomass but caused a shift in soil and rhizosphere fungal community composition, increasing the relative abundance of taxa within the Glomeromycota phylum and decreasing the relative abundance of genera in the Ascomycota phylum, including Lecanicillium, Volutella, Lipomyces, Pochonia, and Rhizoctonia. Our data suggests that tripartite interactions exist between the shoot endophyte E. coenophiala, tall fescue, and soil fungi that may have important implications for the functioning of soils, such as carbon storage, in fescue-dominated grasslands.


Subject(s)
Endophytes/classification , Epichloe/classification , Festuca/microbiology , Soil Microbiology , Archaea/classification , Archaea/isolation & purification , Archaea/metabolism , Bacteria/classification , Bacteria/isolation & purification , Bacteria/metabolism , Chytridiomycota/classification , Chytridiomycota/isolation & purification , Chytridiomycota/metabolism , Endophytes/isolation & purification , Endophytes/metabolism , Epichloe/isolation & purification , Epichloe/metabolism , High-Throughput Nucleotide Sequencing , Soil/chemistry , Symbiosis
13.
Mycologia ; 108(2): 303-12, 2016.
Article in English | MEDLINE | ID: mdl-26740543

ABSTRACT

Litter layers in the Lower Devonian (~ 410 Ma) Rhynie chert were inhabited by a wide variety of saprotrophic fungi, however, only a few of these organisms have been described formally. A new microfungus, Trewinomyces annulifer gen. et sp. nov., occurs as tufts on decaying land plant axes from the Rhynie chert. The fungus consists of an intramatrical rhizoidal system and an erect extramatrical hypha (stalk) that bears a single, terminal sporangium. One or two successive rings often are present in the stalk immediately below the sporangium base. Overall morphology of T. annulifer resembles the extant genera Macrochytrium (Chytridiomycota) and Blastocladiella (Blastocladiomycota). However, the rhizoids are septate or pseudoseptate, a feature not known in extant zoosporic fungi, and thus render the systematic affinities of T. annulifer unresolved. Trewinomyces annulifer offers a rare view of the morphology of a distinctive Early Devonian saprotrophic microfungus.


Subject(s)
Blastocladiomycota/cytology , Chytridiomycota/cytology , Fossils , Blastocladiomycota/classification , Chytridiomycota/classification , Species Specificity
14.
Mycologia ; 108(4): 731-43, 2016.
Article in English | MEDLINE | ID: mdl-27582565

ABSTRACT

Only a few chytrid fungi have been reported as parasites of dinoflagellates. Among these reports, chytrids are periodically observed growing on the dinoflagellate, Peridinium gatunense, in Lake Kinneret (Sea of Galilee), Israel. Because of the distinctive roles of parasitic chytrid fungi in decreasing phytoplankton populations and in transforming inedible algae into chytrid biomass which zooplankton grazers can eat, characterizing dinoflagellate parasites contributes to our understanding of the sustainability of this important water resource. An undescribed chytrid parasite of P. gatunense from Lake Kinneret has recently been brought into pure culture (KLL_TL-060613), facilitating exploration of its infection process. To evaluate the ability of this chytrid to affect host populations, we determined the effect of: (1) temperature and light (or dark) on prevalence of infection and (2) host growth phase and parasite:host ratio on percentage of infection. The greatest amplification in host infection occurred in cultures grown in the dark at 25 C. The percentage of host cells infected increased as the availability of host cells compared to parasite cells increased. These results demonstrate that environmental factors influence the chytrid's potential to affect Peridinium gatunense populations. Because this chytrid had not been described taxonomically, we characterized its thallus morphology, development, zoospore ultrastructure and phylogenetic relationships. Zoospore ultrastructure was compatible with the Group II type zoospore characteristic of the family Chytridiaceae in the Chytridiales. Consistent with this observation, phylogenetic analyses of nuc 28S rDNA D1-D3 domains (28S) placed the chytrid in a clade among described taxa in the Chytridiaceae. Because thallus morphology was distinct from these other taxa, as well as other described parasites of dinoflagellates, this chytrid is described as a new genus and species, Dinochytrium kinnereticum.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Dinoflagellida/microbiology , Chytridiomycota/genetics , Chytridiomycota/physiology , Cluster Analysis , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Host-Parasite Interactions , Israel , Light , Microscopy , Phylogeny , RNA, Ribosomal, 28S/genetics , Sequence Analysis, DNA , Temperature
15.
Mycologia ; 108(4): 744-52, 2016.
Article in English | MEDLINE | ID: mdl-27582566

ABSTRACT

Zoospore ultrastructural characters combined with molecular phylogenetic hypotheses have been used to revise the taxonomy of zoosporic true fungi. An example is the reclassification of Rhizophlyctis rosea-like fungal strains into four new families and three new genera within the order Rhizophlyctidales. One genus was Borealophlyctis, which included a Canadian isolate, DAOMC 229843. A recent survey of chytrid diversity in Alabama (USA) yielded additional strains (WJD 170, WJD 171) in the Borealophlyctis lineage. With light and transmission-electron microscopy we examined strains DAOMC 229843, WJD 170 and WJD 171. We also analyzed partial nuc 28S rDNA D1-D3 domains (28S) and nuc rDNA region encompassing the internal transcribed spacers 1 and 2 and 5.8S (ITS) sequences to determine the phylogenetic placement of the strains within Rhizophlyctidales. Based on molecular divergence and morphological differences from the type Borealophlyctis paxensis, we recognize DAOMC 229843, WJD 170 and WJD 171 as representatives of the new species Borealophlyctis nickersoniae.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Alabama , Canada , Chytridiomycota/cytology , Chytridiomycota/genetics , Cluster Analysis , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Microscopy , Molecular Sequence Data , Phylogeny , RNA, Ribosomal, 28S/genetics , RNA, Ribosomal, 5.8S/genetics , Sequence Analysis, DNA
16.
Dis Aquat Organ ; 112(3): 251-5, 2015 Jan 15.
Article in English | MEDLINE | ID: mdl-25590776

ABSTRACT

We investigated the distribution of Batrachochytrium dendrobatidis (Bd) fungal infections in amphibians of the Western Ghats mountain range in India, based on data from 497 samples. Eight individuals were positive, with genomic equivalents ranging from 2 to 785 zoospores. A single widespread Bd strain identical to the haplotype endemic to Asia was isolated. Our findings suggest that chytridiomycosis is widespread among the endemic and threatened amphibians of the entire stretch of the Western Ghats. An ecological niche-based prediction model based on all Bd-positive reports from the Western Ghats to date suggested a higher probability of infection in the central Western Ghats of Karnataka and northern Kerala states, which host a rich diversity of endemic and threatened amphibians.


Subject(s)
Amphibians , Chytridiomycota/genetics , DNA, Fungal/genetics , Mycoses/veterinary , Animals , Chytridiomycota/classification , Chytridiomycota/isolation & purification , India/epidemiology , Molecular Sequence Data , Mycoses/epidemiology , Mycoses/microbiology , Polymerase Chain Reaction , Sequence Analysis, DNA
17.
Mycologia ; 107(4): 808-30, 2015.
Article in English | MEDLINE | ID: mdl-25911694

ABSTRACT

Many chytrid phylogenies contain lineages representing a lone taxon or a few organisms. One such lineage in recent molecular phylogenies of Rhizophydiales contained two marine chytrids, Rhizophydium littoreum and Rhizophydium aestuarii. To better understand the relationship between these organisms, we increased sampling such that the R. littoreum/R. aestuarii lineage included 10 strains of interest. To place this lineage in Rhizophydiales, we constructed a molecular phylogeny from partial nuc 28S rDNA D1-D3 domains (28S) of these and 80 additional strains in Rhizophydiales and examined thallus morphology and zoospore ultrastructure of our strains of interest. We also analyzed sequences of the nuc rDNA region encompassing the internal transcribed spacers 1 and 2, along with the 5.8S rDNA (ITS) of our 10 strains of interest to assess sequence similarity and phylogenetic placement of strains within the lineage. The 10 strains grouped together in three well supported clades: (i) Rhizophydium littoreum+Phlyctochytrium mangrovei, (ii) three strains of Rhizophydium aestuarii and (iii) five previously unidentified strains. Light microscopic observations revealed four distinct thallus morphologies, and zoospore ultrastructural analyses revealed four distinct constellations of ultrastructural features. On the bases of morphological, ultrastructural and molecular evidence we place these strains in the new family Halomycetaceae and four new genera (Halomyces, Paludomyces, Ulkenomyces, Paranamyces) in Rhizophydiales.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Chytridiomycota/genetics , Chytridiomycota/growth & development , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Molecular Sequence Data , Phylogeny , Spores, Fungal/classification , Spores, Fungal/genetics , Spores, Fungal/growth & development , Spores, Fungal/isolation & purification
18.
Mycologia ; 107(4): 710-28, 2015.
Article in English | MEDLINE | ID: mdl-25911696

ABSTRACT

The evolution of filamentous hyphae underlies an astounding diversity of fungal form and function. We studied the cellular structure and evolutionary origins of the filamentous form in the Monoblepharidomycetes (Chytridiomycota), an early-diverging fungal lineage that displays an exceptional range of body types, from crescent-shaped single cells to sprawling hyphae. To do so, we combined light and transmission electron microscopic analyses of hyphal cytoplasm with molecular phylogenetic reconstructions. Hyphae of Monoblepharidomycetes lack a complex aggregation of secretory vesicles at the hyphal apex (i.e. Spitzenkörper), have centrosomes as primary microtubule organizing centers and have stacked Golgi cisternae instead of tubular/fenestrated Golgi equivalents. The cytoplasmic distribution of actin in Monoblepharidomycetes is comparable to the arrangement observed previously in other filamentous fungi. To discern the origins of Monoblepharidomycetes hyphae, we inferred a phylogeny of the fungi based on 18S and 28S ribosomal DNA sequence data with maximum likelihood and Bayesian inference methods. We focused sampling on Monoblepharidomycetes to infer intergeneric relationships within the class and determined 78 new sequences. Analyses showed class Monoblepharidomycetes to be monophyletic and nested within Chytridiomycota. Hyphal Monoblepharidomycetes formed a clade sister to the genera without hyphae, Harpochytrium and Oedogoniomyces. A likelihood ancestral state reconstruction indicated that hyphae arose independently within the Monoblepharidomycetes lineage and in at least two other lineages. Cytological differences among monoblepharidalean and other fungal hyphae are consistent with these convergent origins.


Subject(s)
Chytridiomycota/cytology , Chytridiomycota/genetics , Phylogeny , Biological Evolution , Chytridiomycota/classification , Chytridiomycota/isolation & purification , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Fungal Proteins/genetics , Hyphae/classification , Hyphae/cytology , Hyphae/genetics , Hyphae/isolation & purification , Molecular Sequence Data
19.
Mycologia ; 107(2): 432-9, 2015.
Article in English | MEDLINE | ID: mdl-25572096

ABSTRACT

Chytriomyces is a complex genus in Chytridiales. The morphological concept of the genus expanded as new taxa were added, and studies of zoospore ultrastructure and molecular phylogenies have revealed the genus to be polyphyletic. One problematic taxon is C. spinosus Fay, a distinctive species characterized by whorls of spines on the zoosporangium and a large accumulation of vesicle material beneath the operculum. With light-, scanning-electron and transmission-electron microscopy, we examined a culture (WJD186) isolated from a muck sample collected from a temporary forest pond. We also analyzed the D1-D2 variable domains of the nuc 28S rDNA (28S) sequences to confirm the phylogenetic placement of the species relative to the type of Chytriomyces, C. hyalinus Karling. The morphology of culture WJD186 is consistent with features Fay described for C. spinosus, and the zoospore ultrastructure is consistent with the Group I-type zoospore characters of Chytriomycetaceae (Chytridiales). In our molecular phylogeny C. spinosus does not group with the type of Chytriomyces. Consequently, we erect a new genus in Chytriomycetaceae and present the new combination Fayochytriomyces spinosus.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Onions/microbiology , Chytridiomycota/genetics , Chytridiomycota/growth & development , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Molecular Sequence Data , Phylogeny , Spores, Fungal/classification , Spores, Fungal/genetics , Spores, Fungal/growth & development , Spores, Fungal/isolation & purification
20.
Mycologia ; 107(2): 419-31, 2015.
Article in English | MEDLINE | ID: mdl-25572098

ABSTRACT

A chytrid first discovered in Mediterranean sands and called Rhizophlyctis harderi was classified in the genus Rhizophlyctis based on its interbiotic vegetative thalli with multiple rhizoidal axes and resting thalli with tufts of rhizoid-like appendages. Developmental, electron microscopic and molecular analyses, however, have brought into question the proper placement of this chytrid. Because its original description was in German and not Latin, the name R. harderi is not validly published. We found that this chytrid produces three thallus forms that could place it in three different morpho-genera: Rhizophydium, Phlyctochytrium or Rhizophlyctis. The ultrastructural architecture of its zoospore is different from that of zoospores of Rhizophlyctis rosea, the type species for Rhizophlyctis, and shares zoospore ultrastructural characteristics with the Rhizophydiales. Zoospores of this chytrid exhibit a distinctive kinetosome-associated structure (KAS), a curved shield bridged to two of the kinetosomal triplets and a layered cap anterior to the kinetosome. Phylogenetic analyses of nuc rDNA also support the placement of this chytrid in the Rhizophydiales and not in the Rhizophlyctidales. Given its molecularly based phylogenetic placement and its distinctive zoospore architecture, we describe this chytrid in a new genus, Uebelmesseromyces, in the Rhizophydiales and erect Uebelmesseromycetaceae as a new family to accommodate it.


Subject(s)
Chytridiomycota/classification , Chytridiomycota/isolation & purification , Chytridiomycota/genetics , Chytridiomycota/growth & development , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Molecular Sequence Data , Phylogeny , Soil Microbiology , Spores, Fungal/classification , Spores, Fungal/genetics , Spores, Fungal/growth & development , Spores, Fungal/isolation & purification
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