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INTRODUCTION<br />

Variability in pathogenicity of Quambalaria pitereka on spotted gums<br />

G.S. Pegg{ XE "Pegg, G.S." } A , A.J. Carnegie B , M.J. Wingfield C , A. Drenth A<br />

A<br />

Tree <strong>Pathology</strong> Centre, The University of Queensland/Primary Industries and Fisheries, Queensland, Australia, 4068<br />

B<br />

Forest Resources Research, NSW Department of Primary Industries, New South Wales, Australia, 2119<br />

C<br />

Forestry and Agricultural Biotechnology Institute, University of Pretoria, South Africa, 0002<br />

Quambalaria shoot blight (QSB) is a serious disease affecting the<br />

expanding eucalypt plantation estate in subtropical and tropical<br />

eastern Australia (1,2). Quambalaria pitereka has been isolated<br />

from foliage, stems and woody tissue of species in the genera<br />

Corymbia, Blakella and Angophora in Australia (1,2,3).<br />

Quambalaria pitereka affects the new flush of Corymbia foliage<br />

causing spotting, necrosis and distortion of expanding leaves and<br />

green stems.<br />

The aim of this investigation was to identify if variation in<br />

pathogenicity levels existed between isolates of Q. pitereka<br />

collected from a range of species and regions in NSW and<br />

Queensland.<br />

MATERIALS AND METHODS<br />

Isolates of Q. pitereka were collected from spotted gum<br />

plantations and Corymbia species trials in north Queensland<br />

(NQ), south east Queensland (SEQ) and northern New South<br />

Wales (NSW). Isolates used were: Q107 from C. torelliana (NQ),<br />

Q147 from C. citriodora (NQ), Q151, Q152 from C. variegata<br />

(SEQ) and Q191, Q200 from C. variegata (NSW).<br />

Spotted gum seedlings (1/2 sibling Woondum provenance) and<br />

cuttings were grown in steam sterilised soil mix and fertilised<br />

with slow release Osmocote ® (Native Trees) as required and<br />

irrigated twice a day for 10 minutes each using overhead<br />

sprinklers. Glasshouse temperatures were maintained at 25–<br />

28°C during the day and 20–22°C overnight. Seedlings were<br />

grown for three months prior to inoculation with Q. pitereka.<br />

QSB Score (x/100)<br />

35<br />

30<br />

25<br />

20<br />

15<br />

10<br />

5<br />

0<br />

Q107 Q147 Q151 Q152 Q191 Q200<br />

Quambalaria pitereka isolate<br />

Figure 1. Comparison of pathogenicity of a range of isolates of<br />

Q. pitereka on spotted gum, Woondum provenance.<br />

DISCUSSION<br />

Variability in pathogenicity between isolates of Q. pitereka has<br />

not previously been studied. This preliminary study using isolates<br />

from a range of regions identifies only a small degree of<br />

variability. More extensive studies are needed to investigate the<br />

significance of pathogen virulence on disease development,<br />

especially in relation to selecting for disease resistance. Further<br />

studies are required to investigate Q. pitereka population<br />

genetics and potential variability in isolate virulence.<br />

ACKNOWLEDGEMENTS<br />

We thank Queensland Primary Industries Innovation and<br />

Biosecurity Program Investment, Forest <strong>Plant</strong>ations Queensland,<br />

Integrated Tree Cropping, Forest Enterprises Australia and<br />

Forests NSW for providing the necessary funding for this<br />

research.<br />

Session 2A—Forest pathology/native<br />

Isolates of Q. pitereka were obtained from single lesions and<br />

grown on Potato Dextrose Agar (PDA) for 2 to 3 weeks in the<br />

dark at 25°C. A spore suspension (1x10 6 spores/ml) was obtained<br />

by washing plates with sterile distilled water (SDW) to which two<br />

drops of Tween 20 had been added prior to inoculation.<br />

Seedlings were inoculated using a fine mist spray (2.9 kPa<br />

pressure) generated by a compressor driven spray gun (Iwata<br />

Studio series 1/6 hp; Gravity spray gun RG3, Portland, USA), to<br />

the upper and lower leaf surfaces of the seedlings until runoff<br />

was achieved. All seedling trees were covered with plastic bags<br />

immediately after inoculation to maintain high humidity levels<br />

and to increase the period of leaf wetness. Bags were removed<br />

after 48 hours and plants watered using overhead irrigation<br />

systems twice a day for a period of 10 minutes. Sub‐samples of<br />

the spore suspension applied to the trees were placed onto PDA<br />

and incubated at 25°C for 48 hours to ensure that the spores<br />

were viable.<br />

REFERENCES<br />

1. Carnegie AJ, 2007a. Forest health condition in New South Wales,<br />

Australia, 1996–2005. I. Fungi recorded from eucalypt plantations<br />

during forest health surveys. <strong>Australasian</strong> <strong>Plant</strong> <strong>Pathology</strong> 36, 213–<br />

24.<br />

2. Pegg GS, O’Dwyer C, Carnegie AJ, Wingfield MJ, Drenth A 2008.<br />

Quambalaria species associated with plantation and native<br />

eucalypts in Australia. <strong>Plant</strong> <strong>Pathology</strong> 57, 702–14.<br />

3. Simpson JA, 2000. Quambalaria, a new genus of eucalypt<br />

pathogens. <strong>Australasian</strong> Mycologist 19, 57–62.<br />

Each treatment was replicated six times with a single inoculation<br />

per tree and assessed for disease incidence and severity 14 days<br />

later. A QSB score was then calculated to compare levels of<br />

pathogenicity between isolates. A comparison between isolates<br />

was done using ANOVA (Stat<strong>View</strong>®).<br />

RESULTS<br />

Significant variability in pathogenicity was observed between<br />

isolates. Isolate Q152 was significantly more virulent than all<br />

other isolates.<br />

APPS 2009 | PLANT HEALTH MANAGEMENT: AN INTEGRATED APPROACH 35

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