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Inoculum 63(3) - Mycological Society of America

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ular soil horizons, the isotopic composition <strong>of</strong> macr<strong>of</strong>ungal fruiting bodies might<br />

be a useful tool for tracing lead origin. Our preliminary data from a case study in<br />

Agaricus bernardii have supported this hypothesis. Furthermore, the isotopic<br />

composition <strong>of</strong> lead in saprotrophic macr<strong>of</strong>ungi (Agaricus campestris, A.<br />

bernardii, A. xanthodermus and Leucoagaricus leucothites) <strong>of</strong> various origins has<br />

reflected more or less the expected pollution sources.<br />

Brewer, Marin T and Ashley N Turner. Department <strong>of</strong> Plant Pathology, University<br />

<strong>of</strong> Georgia, Athens, GA 30602. Genetic diversity and reproductive isolation<br />

in Didymella bryoniae, a fungal pathogen <strong>of</strong> cucurbits<br />

We are interested in determining the center <strong>of</strong> diversity, as well as historical<br />

and ongoing migration patterns in the cucurbit pathogen Didymella bryoniae.<br />

This fungus causes gummy stem blight and black rot <strong>of</strong> cucurbits everywhere they<br />

are grown, yet relatively little is known about how it is dispersed. Previous studies<br />

with dominant markers have indicated that this species is diverse and contains<br />

at least two distinct genetic groups. We sequenced four nuclear regions, including<br />

calmodulin (CAL), beta-tubulin (TUB2), chitin synthase 1 (CHS-1), and the internal<br />

transcribed spacer <strong>of</strong> the rDNA (ITS) <strong>of</strong> thirty-four isolates from diverse cucurbit<br />

hosts across the United States (US). Isolates from both genetic groups were<br />

represented in our sample. A total <strong>of</strong> 1415 bp were sequenced, resulting in 41<br />

polymorphic sites and 13 unique haplotypes. A haplotype network constructed<br />

with TCS demonstrated that there are two distinct genetic groups, which is consistent<br />

with previous studies. However, a single isolate collected from a greenhouse<br />

in California was quite distinct from both groups. There is no association<br />

with genetic group and host species <strong>of</strong> origin, which is not surprising because earlier<br />

studies indicated that host specialization is not evident with D. bryoniae. Geographic<br />

associations were detected, however, as one <strong>of</strong> the groups was present<br />

only in the northeastern US whereas the other group was found throughout the<br />

US. There are no detectable morphological differences between the two genetic<br />

groups indicating that these groups represent cryptic species that are reproductively<br />

isolated. Studies on a worldwide collection <strong>of</strong> isolates are currently underway.<br />

Coalescent analyses on this collection will be aimed at understanding migration<br />

patterns, geographic origin, and approximate age <strong>of</strong> the divergence <strong>of</strong> the<br />

genetic groups to elucidate the evolutionary processes contributing to the observed<br />

patterns <strong>of</strong> diversity.<br />

Broders, Kirk 1 , Andre Boraks 1 , Laura Barbison 2 , John Brown 2 , and Greg<br />

Boland 2 . 1 Department <strong>of</strong> Biological Sciences, University <strong>of</strong> New Hampshire,<br />

Durham, NH 03824, 2 School <strong>of</strong> Environmental Sciences, University <strong>of</strong> Guelph,<br />

Guelph, ON N1G 2W1. Invasion biology <strong>of</strong> the butternut canker fungus<br />

Ophiognomonia clavigignenti-juglandacearum<br />

Butternut canker caused by the fungal pathogen Ophiognomonia<br />

clavigignenti-juglandacearum (Oc-j) remains the primary cause for range-wide<br />

mortality <strong>of</strong> butternut trees. The disease was first reported in Wisconsin in 1967,<br />

however the fungus may have been present for several years prior. Several questions<br />

still remain largely unanswered regarding the invasion by Oc-j. These questions<br />

include; how many times was the fungus introduced; where was it introduced;<br />

were more virulent strains introduced; and how was it able to spread so<br />

rapidly within the native butternut population. Therefore, our objective was to<br />

evaluate the invasion biology <strong>of</strong> this fungus including investigations into the ecology,<br />

epidemiology, and population structure <strong>of</strong> Oc-j in North <strong>America</strong>. To complete<br />

these objective flowers, developing seeds, and mature seeds <strong>of</strong> butternut,<br />

heartnut and black walnut were assessed as potential vectors <strong>of</strong> Oc-j; Sixteen isolates<br />

were evaluated for virulence on butternut, heartnut, and black walnut; and<br />

100 isolates <strong>of</strong> Oc-j from across North <strong>America</strong> were used to analyze the population<br />

structure <strong>of</strong> the fungus. Bayesian analyses based on 16 SNP markers revealed<br />

that the Oc-j population in North <strong>America</strong>n is composed <strong>of</strong> four genetically distinct<br />

clonal lineages, suggesting multiple introductions <strong>of</strong> Oc-j, through successive<br />

or simultaneous introductions <strong>of</strong> isolates having differentiated genetic backgrounds.<br />

Isolates <strong>of</strong> Oc-j recovered from heartnut and black walnut caused larger<br />

lesions on all three Juglans species compared to isolates originally recovered from<br />

butternut. Four <strong>of</strong> the five isolates, which caused the largest lesions on butternut<br />

belonged to a single genetic cluster. The pathogenicity data in combination with<br />

geographic and population structure data indicate this fungus was introduced into<br />

North <strong>America</strong> on multiple occasions, and a more virulent clonal lineage was recently<br />

introduced into Minnesota and Wisconsin and subsequently spread<br />

throughout the rest <strong>of</strong> the butternut canker population in North <strong>America</strong>.<br />

Buchanan, Peter K and Peter R Johnston. Landcare Research, Private Bag<br />

92170, Auckland 1142, New Zealand. Conservation <strong>of</strong> Fungi - threat status <strong>of</strong><br />

fungi in New Zealand and globally<br />

Fungi have been included in threat status assessments <strong>of</strong> New Zealand’s<br />

biota since 2002. Assessments have mainly addressed macr<strong>of</strong>ungi, as well as obligate<br />

species <strong>of</strong> fungi on threatened plants. The initial inclusion <strong>of</strong> fungi, and subsequent<br />

need for reassessment <strong>of</strong> threat status, has generated new research initiatives<br />

and raised awareness <strong>of</strong> fungal conservation. Aspects <strong>of</strong> fungal biology such<br />

12 <strong>Inoculum</strong> <strong>63</strong>(3), June 2012<br />

as ephemeral reproductive stages add difficulty to threat status assessments. Examples<br />

are presented <strong>of</strong> fungal species listed in the highest (Nationally Critical)<br />

and other threat categories. Over 1,000 species <strong>of</strong> fungi are listed as Data Deficient<br />

due to inadequate distribution data. Fungi have been included in a prioritization<br />

exercise spanning all New Zealand’s threatened taxa that are in decline, to<br />

evaluate methodology, feasibility, and cost <strong>of</strong> long-term recovery plans. Using<br />

molecular techniques, new records <strong>of</strong> ectomycorrhizal fungi listed as Data Deficient<br />

have been discovered by comparing environmental sampling <strong>of</strong> ectomycorrhizas<br />

with DNA sourced from herbarium specimens. Responding to increasing<br />

global awareness <strong>of</strong> the need for fungal conservation, the International <strong>Society</strong> for<br />

Conservation <strong>of</strong> Fungi was formed in 2010, and five Fungal Specialist Groups<br />

have been established under IUCN.<br />

Burchhardt, Kathleen M and Marc A Cubeta. North Carolina State University,<br />

Department <strong>of</strong> Plant Pathology, Raleigh, NC 27695. Population dynamics <strong>of</strong><br />

Monilinia vaccinii-corymbosi in blueberry fields throughout the United<br />

States<br />

Mummy berry disease <strong>of</strong> blueberry (Vaccinium spp.) is caused by the ascomycete<br />

Monilinia vaccinii-corymbosi (Mvc). The fungus produces asexual and<br />

sexual spores that infect blueberry shoots and fruit. While spore dispersal and sexual<br />

reproduction can contribute to the spread and evolution <strong>of</strong> fungal populations,<br />

little is known about the population dynamics <strong>of</strong> Mvc. The primary objective <strong>of</strong><br />

this study was to utilize microsatellite-based genetic markers to examine intraspecific<br />

genetic diversity, population structure, and gene flow among populations<br />

<strong>of</strong> Mvc throughout blueberry growing regions <strong>of</strong> the United States. In this<br />

study, 438 isolates <strong>of</strong> Mvc sampled from 15 blueberry fields in New York, New<br />

Jersey, Massachusetts, Georgia, Mississippi, Oregon, Washington, Michigan, and<br />

North Carolina were screened with 10 polymorphic microsatellite markers. Results<br />

based on analyzing a geographically diverse subsample <strong>of</strong> 55 isolates from<br />

six fields indicate high intraspecific genetic diversity. Forty-eight private alleles<br />

were detected across the 10 loci, providing evidence for population differentiation<br />

and restricted gene flow among fields. Results from population genetic analyses<br />

<strong>of</strong> a more comprehensive dataset <strong>of</strong> 438 isolates will be presented.<br />

Burleigh, J Gordon 1 , Keith Crandall 2 , Karen Cranston 3 , Karl Gude 4 , David S<br />

Hibbett 5 , Mark Holder 6 , Laura A Katz 7 , Richard H Ree 7 , Stephen A Smith 7 ,<br />

Douglas E Soltis 7 , and Tiffani Williams 7 . 1 Department <strong>of</strong> Biology, University <strong>of</strong><br />

Florida, Gainesville, FL 32611, 2 Department <strong>of</strong> Biology, Brigham Young University,<br />

Provo, UT 84602, 3 NESCENT, Durham, NC 27705, 4 College <strong>of</strong> Communication,<br />

5<br />

Arts and Sciences, Michigan State University, E. Lansing<br />

6<br />

MI 45622,<br />

Biology Department, Clark University, Worcester MA 01610, Department <strong>of</strong><br />

Ecology<br />

7<br />

and Evolutionary Biology, University <strong>of</strong> Kansas, Lawrence KS 66045,<br />

and elsewhere. Open Tree <strong>of</strong> Life: Community driven synthesis <strong>of</strong> the Tree<br />

<strong>of</strong> Life<br />

Reconstructing the phylogeny <strong>of</strong> all species has been a grand challenge<br />

ever since Darwin. The scope <strong>of</strong> the problem is immense: current estimates <strong>of</strong> extant<br />

biodiversity range from 1.8 million to 8.7 million species, a large fraction <strong>of</strong><br />

which are Fungi. Much progress has recently been made in resolving the tree, and<br />

systematists continue to generate new phylogenetic knowledge at all depths <strong>of</strong> ancestry.<br />

Nevertheless, despite 150 years <strong>of</strong> effort, 55 AToL projects, and numerous<br />

other funded projects, we lack a comprehensive tree <strong>of</strong> life. Synthesis is currently<br />

inhibited by limits <strong>of</strong> available data, analytical power, and informatics infrastructure.<br />

Perhaps more importantly, it is also limited by a lack <strong>of</strong> compelling<br />

means and incentives for community participation. A comprehensive synthesis<br />

would yield great benefits across the life sciences, especially if it were self-sustaining,<br />

community-driven, and continually updated. We describe a recently funded<br />

project named “Open Tree <strong>of</strong> Life” that aims to establish a community-driven,<br />

continually updated estimate <strong>of</strong> the entire tree, and develop new s<strong>of</strong>tware tools<br />

and new methods for merging and sharing data. Open Tree <strong>of</strong> Life will: 1) within<br />

one year, compile the first comprehensive draft tree <strong>of</strong> life by synthesizing existing<br />

phylogenetic and taxonomic knowledge; 2) enable the community to improve,<br />

annotate, and expand this initial tree; 3) initiate a cultural transformation in<br />

systematics towards pervasive and ingrained practices <strong>of</strong> data sharing; and 4) develop<br />

novel methods for synthetic tree reconstruction. By engaging the systematics<br />

community, including mycologists, our overarching goal is to cultivate ongoing<br />

synthesis on a large scale, in a manner that will transform current cultural<br />

norms in the field.<br />

Bushley, Kathryn E and Joseph W Spatafora. Department <strong>of</strong> Botany and Plant<br />

Pathology, Oregon State University, Corvallis, OR 97330. Convergent and divergent<br />

evolution <strong>of</strong> nonribosomal peptide synthetases<br />

Nonribosomal peptide synthetases (NRPSs) are large multimodular enzymes<br />

which produce small bioactive peptides (NRPs) without the aid <strong>of</strong> ribosomes.<br />

While the function <strong>of</strong> many NRPs remains unknown, it is becoming clear<br />

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