09.04.2013 Views

March 2008 - Mycological Society of America

March 2008 - Mycological Society of America

March 2008 - Mycological Society of America

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

communities <strong>of</strong> a particular parasitoid wasp, Comperia merceti (Hymenoptera:<br />

Encyrtidae), and the cockroach it parasitizes, Supella longipalpa<br />

(Blattaria: Blattellidae), are examined using both molecular- and<br />

culture-based methods. From LSU cloning data there is evidence <strong>of</strong><br />

two fungi in the wasps (basidiomycete relatives), and three fungi in the<br />

cockroaches. Two <strong>of</strong> the cockroach fungal symbionts are identical to<br />

the basidiomycete relatives recovered from wasps and there is an additional<br />

lecanoromycete relative. Using general 16S primers, Blattabacterium<br />

and Wolbachia are also recovered from the cockroaches. Culturing<br />

efforts reveal that only one <strong>of</strong> the basidiomycete-like fungi from<br />

the wasps is cultivable and an additional (possibly nitrogen fixing) bacterium<br />

is cultivable from the cockroaches. The characterization <strong>of</strong> the<br />

microbial associates in this system lays the foundation for understanding<br />

symbiont contributions to these wasps and cockroaches. This research<br />

reveals cryptic fungal diversity in an understudied niche, insect<br />

hosts, as well as demonstrates the role that fungi could have in shaping<br />

the evolution <strong>of</strong> host-parasitoid interactions. Poster<br />

Gillevet, Patrick, M., Sikaroodi, M. and Torzilli, Albert, P.* Department<br />

<strong>of</strong> Environmental Science and Policy, George Mason University,<br />

Fairfax, VA 22030, USA. atorzill@gmu.edu. Analysing salt-marsh<br />

fungal community diversity: community ARISA fingerprinting vs.<br />

community clone sequencing. Fungi are important decomposers in<br />

the detrital-based food webs <strong>of</strong> temperate salt-marsh ecosystems.<br />

Knowing the composition <strong>of</strong> salt-marsh fungal communities is essential<br />

for understanding how detritus processing is affected by changes in<br />

community dynamics. Previous results from our laboratory have<br />

shown that different salt-marsh plants harbor distinct fungal communities<br />

as judged by automated ribosomal intergenic spacer analysis<br />

(ARISA) <strong>of</strong> fungal DNA amplified from the different plant hosts.<br />

ARISA fingerprinting data provide non-taxon-specific snapshots <strong>of</strong><br />

community structure where each peak in a community pr<strong>of</strong>ile represents<br />

an operational taxonomic unit (OTU) <strong>of</strong> a given amplicon size. In<br />

order to associate specific taxa with community OTUs we cloned, fingerprinted,<br />

and sequenced the fungal community DNA from each plant<br />

in order to match the size and sequence <strong>of</strong> specific clones with the community<br />

OTU sizes. BLAST results indicated that a given OTU amplicon<br />

may represent more than one species, confirming earlier observations.<br />

Also, the ability to assign a specific taxon to a community<br />

amplicon by matching amplicon sizes was limited by the extent <strong>of</strong><br />

species coverage in the BLAST database. Furthermore, differences in<br />

the relative abundances between community fingerprint amplicons and<br />

comparable clone abundances suggested significant biases during the<br />

cloning process. Nonetheless, the cloning and sequencing data did confirm<br />

the conclusion from fingerprinting that plant (substrate) type is an<br />

important factor in determining fungal community composition. Poster<br />

Goldmann, Lauren* and Weir, Alex. Department <strong>of</strong> Environmental &<br />

Forest Biology, SUNY College <strong>of</strong> Environmental Science & Forestry,<br />

241 Illick Hall, 1 Forestry Drive, Syracuse, NY 13210, USA. lmgold01@syr.edu.<br />

Laboulbeniales from western Russia. As a part <strong>of</strong><br />

the SUNY-ESF Moscow State University Exchange Program we had<br />

the opportunity in summer 2006 to collect Laboulbeniales fungi at the<br />

Zvenigorod Biological Station, some 50km west <strong>of</strong> Moscow, and at the<br />

White Sea Biological Station near Poiakonda. The most recent literature<br />

<strong>of</strong> the Laboulbeniales <strong>of</strong> the western portion <strong>of</strong> Russia is that by Hulden<br />

(1983), who records 41 species. Our collections have added an additional<br />

10 species, including 3 new genera for the region; Aphanandromyces,<br />

Euzodiomyces, and Rhadinomyces. Of particular interest was<br />

our observation <strong>of</strong> very high levels <strong>of</strong> infection at both these sites with<br />

15% <strong>of</strong> collected beetles infected at Zvenigorod, and 14% at the White<br />

Sea. These figures are much higher than those recorded by Hulden (1%)<br />

and may be related to the range <strong>of</strong> microhabitats sampled. Poster<br />

Gonzalez, Maria C. 1 * and Enriquez, Diana. 21 Departamento de Botanica<br />

AP 70-233, Instituto de Biologia, Universidad Nacional Autonoma<br />

de Mexico, Ciudad de Mexico DF 04510, Mexico, 2 Instituto de<br />

Oceanologia, Agencia del Medio Ambiente, Ministerio de Ciencia, Tecnologia<br />

y Medio Ambiente de Cuba (CITMA), La Habana, Cuba.<br />

18 Inoculum 59(2), <strong>March</strong> <strong>2008</strong><br />

mcgv@ibiologia.unam.mx. Micr<strong>of</strong>ungi diversity in the coastal sand<br />

beach environment <strong>of</strong> Mexico and Cuba. The marine interstitial micr<strong>of</strong>ungi<br />

living in sandy sediments between the tide lines <strong>of</strong> the beaches<br />

are important ecologically because they are major decomposers <strong>of</strong> the<br />

vegetable organic matter that enter this marine ecosystem. In this particular<br />

environment, named endopsammon, the microbial production is<br />

dominated by eumycotes, mainly by ascomycetes. Arenicolous micr<strong>of</strong>ungi<br />

have a distinctive physiology, morphology, and adaptation to the<br />

endopsammophilous medium. The characteristics that the arenicolous<br />

species exhibit are: carbonaceous ascocarps attached to sand grains with<br />

a subiculum, papilla with an ostiole opening close to the subiculum, a<br />

pseudoparenchyma <strong>of</strong> thin walled cells with pit-like thickenings, deliquescent<br />

asci without an apical structure, and appendaged ascospores.<br />

The genus Corollospora is considered as one <strong>of</strong> the most diverse genera<br />

adapted to arenicolous habitats and is distributed widely from tropical to<br />

temperate regions. During the past decade, a surge has taken place in the<br />

investigation <strong>of</strong> the Mexican and Cuban arenicolous micr<strong>of</strong>ungi biodiversity.<br />

At present, these countries have an active interest in describing,<br />

preserving, and using the biodiversity <strong>of</strong> marine fungi. The advances in<br />

recording the distribution <strong>of</strong> species from several beaches <strong>of</strong> Mexico<br />

and Cuba are presented. Symposium Presentation<br />

Gross, Stephanie*, Suh, Sung-Oui and Blackwell, Meredith. Department<br />

<strong>of</strong> Biological Sciences, Louisiana State University, Baton Rouge,<br />

Louisiana 70803, USA. sgross2@lsu.edu. Diet and its effect on the<br />

abundance <strong>of</strong> endosymbiotic gut yeast found in a wood-boring beetle<br />

Odontotaenius disjunctus: Passalidae. Pichia stipitis, a xylose fermenting<br />

and assimilating yeast, has consistently been isolated from the<br />

gut <strong>of</strong> over 400 adult, wood-boring beetles (Odontotaenius disjunctus:<br />

Passalidae). We examined the affect <strong>of</strong> beetle diet on gut yeasts by varying<br />

nutrients provided for the host beetles. Beetles were provided only<br />

autoclaved water and starved for 6 da and then were fed different diets,<br />

(e.g., decayed wood, sterilized decayed wood, and artificial diet containing<br />

polysaccharides and other nutritional resources). Beetles were<br />

dissected periodically and yeast colony counts were made on selective<br />

agar media. Colonies on each plate were identified based on morphology,<br />

and some were confirmed as P. stipitis by use <strong>of</strong> specific primers.<br />

After 6 da starvation, the abundance <strong>of</strong> P. stipitis in the gut decreased<br />

substantially when compared to pre-starvation numbers. However, 5 da<br />

after reintroduction <strong>of</strong> food, yeast numbers in the gut increased to approximately<br />

pre-starvation levels. We observed no significant difference<br />

in colony numbers between beetles fed unsterilized and sterilized wood,<br />

but beetles fed certain diets sometimes had low levels <strong>of</strong> yeasts compared<br />

to those fed wood. From this study, we concluded that within the<br />

O. disjunctus gut environment P. stipitis is dependent on nutrients provided<br />

by the insect diet. Contributed Presentation<br />

Guardia Valle, Laia 1 and Cafaro, Matias J. 2 * 1 Unitat Botanica Dep.<br />

BABVE F. Ciences, Universitat Autonoma de Barcelona, 08193 Bellaterra,<br />

Spain, 2 Department <strong>of</strong> Biology, University <strong>of</strong> Puerto Rico –<br />

Mayaguez, PR 00681. matcaf@gmail.com. First observation <strong>of</strong> zygospores<br />

in Asellariales (Trichomycetes). The ecological group <strong>of</strong><br />

gut endosymbionts trichomycetes (sensu lato) includes two fungal orders,<br />

Harpellales and Asellariales, and two protistan orders, Amoebidiales<br />

and Eccrinales. Asellariales inhabit the digestive tract <strong>of</strong> aquatic,<br />

terrestrial and marine isopods as well as springtails (Collembola). They<br />

have branched and septated thalli and reproduce asexually by<br />

arthrospore-like cells. No sexual reproduction has been reported until<br />

now. In a recent survey <strong>of</strong> islands in the Carribean, a new unnamed<br />

species <strong>of</strong> Asellaria has been found in terrestrial isopods in Puerto Rico<br />

and Dominican Republic. Conjugating tubes and zygospores were observed<br />

in this Asellaria sp. Zygospores are spherical and hyaline in contrast<br />

to the ones in Harpellales, which are conical or biconical. Asellariales<br />

zygospores share characteristics with those <strong>of</strong> Dimargaritales and<br />

Kickxellales as well as their septal pore structure, which is present in<br />

all three orders plus the Harpellales, thus giving morphological support<br />

to this monophyletic group, recently established through DNA analyses.<br />

The spherical shape <strong>of</strong> Asellaria zygospores reveals a possible ter-<br />

Continued on following page

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!