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. 2011;6(10):e26445.
doi: 10.1371/journal.pone.0026445. Epub 2011 Oct 26.

Molecular diversity of fungal phylotypes co-amplified alongside nematodes from coastal and deep-sea marine environments

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Molecular diversity of fungal phylotypes co-amplified alongside nematodes from coastal and deep-sea marine environments

Punyasloke Bhadury et al. PLoS One. 2011.

Abstract

Nematodes and fungi are both ubiquitous in marine environments, yet few studies have investigated relationships between these two groups. Microbial species share many well-documented interactions with both free-living and parasitic nematode species, and limited data from previous studies have suggested ecological associations between fungi and nematodes in benthic marine habitats. This study aimed to further document the taxonomy and distribution of fungal taxa often co-amplified from nematode specimens. A total of 15 fungal 18S rRNA phylotypes were isolated from nematode specimens representing both deep-sea and shallow water habitats; all fungal isolates displayed high pairwise sequence identities with published data in Genbank (99-100%) and unpublished high-throughput 454 environmental datasets (>95%). BLAST matches indicate marine fungal sequences amplified in this study broadly represent taxa within the phyla Ascomycota and Basidiomycota, and several phylotypes showed robust groupings with known taxa in phylogenetic topologies. In addition, some fungal phylotypes appeared to be present in disparate geographic habitats, suggesting cosmopolitan distributions or closely related species complexes in at least some marine fungi. The present study was only able to isolate fungal DNA from a restricted set of nematode taxa; further work is needed to fully investigate the taxonomic scope and function of nematode-fungal interactions.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Maximum likelihood tree with bootstrap values constructed using fungal 18S rRNA sequences generated from this study and corresponding BLAST matches with highly identity scores recovered from GenBank and EMBL as well as published cultured fungal 18S rRNA sequences.
Bootstrap values for nodes greater than 50% are shown in the tree. The scale bar indicates 0.05 substitution per site.

References

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