06.04.2013 Views

Book of Abstracts (PDF) - International Mycological Association

Book of Abstracts (PDF) - International Mycological Association

Book of Abstracts (PDF) - International Mycological Association

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

IMC7 Main Congress Theme III: PATHOGENS AND NUISANCES, FOOD AND MEDICINE Posters<br />

864 - Simultaneous detection <strong>of</strong> GFP- and GUS-marked<br />

fungi <strong>of</strong> different formae speciales <strong>of</strong> Fusarium<br />

oxysporum on plant roots<br />

T. Nonomura * , Y. Matsuda & H. Toyoda<br />

Laboratory <strong>of</strong> Plant Pathology and Biotechnology, Faculty<br />

<strong>of</strong> Agriculture, Kinki University, 3327-204 Nakamachi<br />

Nara 631-8505, Japan. - E-mail:<br />

nonomura@nara.kindai.ac.jp<br />

In our attempt to visualize infection behavior <strong>of</strong> the fungal<br />

wilt pathogens inoculated onto plant roots, the fungi were<br />

genetically marked with two reporter genes. F. oxysporum<br />

f. sp. lycopersici (FOL) and F. o. f. sp. melonis (FOM)<br />

were transformed with the green fluorescence protein gene<br />

(GFP) and the β-glucuronidase gene (GUS), respectively.<br />

In the present study, we focused mainly on the attachment<br />

and subsequent hyphal elongation by microconidia<br />

inoculated onto roots <strong>of</strong> tomato and melon seedling. In<br />

addition, we attempted to directly distinguish different<br />

formae speciales <strong>of</strong> F. oxysporum onto the same plant roots<br />

by expression <strong>of</strong> different marker genes. Microconidia <strong>of</strong><br />

GFP-marked FOL (KFOL-001) and GUS-marked FOM<br />

(KFOM-002) were inoculated onto roots <strong>of</strong> cotyledonal<br />

seedlings, and inoculated roots were first observed under a<br />

fluorescence microscope to detect KFOL-001 and then<br />

stained with X-gluc (substrate for GUS assay) to detect<br />

KFOM-002 under a light microscope. Consequently, both<br />

transformed pathogens could be clearly distinguished at the<br />

same site <strong>of</strong> inoculation. These results suggest that dual<br />

transformation <strong>of</strong> F. oxysporum is useful for analyzing<br />

behavior <strong>of</strong> nonpathogenic F. oxysporum challengeinoculated<br />

with pathogenic F. oxysporum.<br />

865 - Biscogniauxia and Daldinia; latent pathogens <strong>of</strong><br />

deciduous trees<br />

L.K. Nugent * , G.P. Sharples & A.J.S. Whalley<br />

School <strong>of</strong> Biomoleculr Sciences, Liverpool John Moores<br />

University, Byrom Street, Liverpool L3 3AF, U.K. - E-mail:<br />

beslnuge@livjm.ac.uk<br />

Biscogniauxia Kuntze and Daldinia Ces. and De Not. are<br />

two wood inhabiting xylariaceous genera. Biscogniauxia<br />

species are frequently linked with canker diseases in<br />

stressed hosts e.g. B. mediterranea causes coal canker in<br />

Quercus suber (cork oak) and B. nummularia canker in<br />

Fagus (beech) while D. concentrica (Bolt. ex. Fr.) causes<br />

calico wood in Fraxinus (ash). Studies on ascospore<br />

germination and development <strong>of</strong> the anamorphs in culture<br />

in response to host extracts is presented. Biscogniauxia<br />

nummularia and Daldinia concentrica. have been isolated<br />

from their respective host leaves and branches and there are<br />

frequency <strong>of</strong> isolation maybe linked to ascospore<br />

production. The presence <strong>of</strong> Daldinia in leaves and in<br />

wood has been investigated microscopically, chemically<br />

and by molecular techniques, in addition to traditional<br />

isolation techniques following surface sterilisation. The<br />

260<br />

<strong>Book</strong> <strong>of</strong> <strong>Abstracts</strong><br />

presence <strong>of</strong> latent pathogens and their relationship to stress<br />

<strong>of</strong> the host is presented. Experimentation on conditions<br />

leading to the latent invasion and subsequent development<br />

<strong>of</strong> teliomorphs are being undertaken in both field and<br />

laboratory.<br />

866 - Establishment <strong>of</strong> the first Karnal Bunt testing<br />

laboratory in South Africa<br />

O.M. O'Brien, I.H. Rong * & E.J. van der Linde<br />

ARC-Plant Protection Research Institute, Private Bag<br />

X134, Pretoria 0001, South Africa.<br />

The fungal wheat disease Tilletia indica, commonly known<br />

as Karnal Bunt (KB), was detected in a limited area <strong>of</strong> one<br />

<strong>of</strong> South Africa's wheat producing regions during 1999.<br />

Aimed at managing T. indica, a national survey to<br />

determine the occurrence <strong>of</strong> the disease was initiated by the<br />

Directorate Plant, Health and Quality, National Department<br />

<strong>of</strong> Agriculture. To this end, the Mycology Unit, ARC-Plant<br />

Protection Research Institute, Pretoria was tasked with<br />

setting up a laboratory for the analyses <strong>of</strong> seed and grain<br />

samples. Due consideration was given to the geographical<br />

distance <strong>of</strong> the laboratory from the main wheat producing<br />

areas <strong>of</strong> the country. The KB protocol, as recommended by<br />

the USDA/APHIS, was followed with some adaptations.<br />

Analyses were conducted for two consecutive years,<br />

providing valuable experience in managing a quarantine<br />

analytical facility <strong>of</strong> this nature. Protocols and procedures<br />

representing different phases <strong>of</strong> the process were devised<br />

for each workstation. These phases included: reception and<br />

registering <strong>of</strong> samples, sub-sampling, washing and sieving,<br />

centrifuging and preparing <strong>of</strong> microscope slides, detection<br />

<strong>of</strong> T. indica, data processing and reporting, and waste<br />

management. Laboratory procedures, problems<br />

encountered and the development <strong>of</strong> novel techniques, as<br />

well as the management and maintenance <strong>of</strong> the quarantine<br />

facility, are discussed.<br />

867 - Aflatoxins in the weaning food <strong>of</strong> Kenyan children<br />

S.A. Okoth<br />

Botany Department, University <strong>of</strong> Nairobi, P. O. Box<br />

30197, Nairobi, Kenya. - E-mail: dorisokoth@yahoo.com<br />

Cereal grains run a high risk <strong>of</strong> mycotoxin contamination<br />

yet they form the basis <strong>of</strong> gruels used in weaning children<br />

in Kenya. To these grains (maize, sorghum, millet)<br />

supplements such as cassava, groundnuts, beans, and fish<br />

are added and ground together, depending on the means<br />

and education <strong>of</strong> the parents. Among the mycotoxins,<br />

aflatoxins have been implicated in human diseases,<br />

including kwashiorkor. Sampling for aflatoxin<br />

contamination was done in Kisumu District, Kenya, an area<br />

with high relative humidity and temperatures, high<br />

incidence <strong>of</strong> kwashiorkor and the highest prevalence <strong>of</strong><br />

absolute poverty, 63%, in the country. A total <strong>of</strong> 180

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

Saved successfully!

Ooh no, something went wrong!