Citrus canker is a disease of citrus and closely related species, caused by the bacterium Xanthomonas citri subsp. citri. This disease, previously exotic to Australia, was detected on a single farm [infested premise-1, (IP1). IP is the terminology used in official biosecurity protocols to describe a locality at which an exotic plant pest has been confirmed or is presumed to exist. IP are numbered sequentially as they are detected] in Emerald, Queensland in July 2004. During the following 10 months the disease was subsequently detected on two other farms (IP2 and IP3) within the same area and studies indicated the disease first occurred on IP1 and spread to IP2 and IP3. The oldest, naturally infected plant tissue observed on any of these farms indicated the disease was present on IP1 for several months before detection and established on IP2 and IP3 during the second quarter (i.e. autumn) 2004. Transect studies on some IP1 blocks showed disease incidences ranged between 52 and 100% (trees infected). This contrasted to very low disease incidence, less than 4% of trees within a block, on IP2 and IP3. The mechanisms proposed for disease spread within blocks include weatherassisted dispersal of the bacterium (e.g. wind-driven rain) and movement of contaminated farm equipment, in particular by pivot irrigator towers via mechanical damage in combination with abundant water. Spread between blocks on IP2 was attributed to movement of contaminated farm equipment and/or people. Epidemiology results suggest: (i) successive surveillance rounds increase the likelihood of disease detection; (ii) surveillance sensitivity is affected by tree size; and (iii) individual destruction zones (for the purpose of eradication) could be determined using disease incidence and severity data rather than a predefined set area.
Tobacco streak virus (genus Ilarvirus) is recorded on sunflower (Helianthus annuus), cotton (Gossypium hirsutum), chickpea (Cicer arietinum) and mung bean (Vigna radiata) in Australia for the first time. (a) (c) CSIRO PUBLISHING www.publish.csiro.au/journals/apdn
When sap of asymptomatic or mealybug wilt-affected pineapple plants of the Smooth Cayenne group was negatively stained and examined in an electron microscope, clostero-like virus particles were occasionally seen. However, numerous clostero-like virus particles and occasionally some bacilliform particles were seen in partially purified preparations from both asymptomatic and wilted pineapple leaves. An antiserum, made by injecting partially purified preparations of clostero-like particles into a rabbit, trapped and decorated the clostero-like particles. Using this antiserum, the clostero-like particles (c. 1700 -1900x12 nm) were found in almost all plants tested of Smooth Cayenne selections C10, C13, C30 and F-180, the hybrid cv. 53-116 and a selection of the rough leaf Queen group. The particles were more readily trapped from extracts of roots of hybrid cv. 53-116 and Smooth Cayenne selection C10 than from leaves, crowns and fruits. They were not detected in seedlings of a cross between a Queen selection and the Smooth Cayenne selection C10. The clostero-like particles are similar to those reported to occur in pineapple plants in Hawaii and South Africa. This is the first report of their occurrence in Australia. Trapping and decoration tests of particles in pineapples in quarantine from Brazil, France, Malaysia and Taiwan indicated that a similar clostero-like virus occurs in all these countries. The bacilliform particles measured about 133x33 nm. They were trapped and decorated by the Queensland pineapple virus antiserum and also by an antiserum to sugarcane bacilliform badnavirus. They were detected occasionally in various smooth leaf and rough leaf pineapples in north and south Queensland and northern New South Wales. However, in one commercial planting of Smooth Cayenne selection C10 in south Queensland, bacilliform particles were trapped from 29/47 plants. This is the first report of a small bacilliform virus, probably belonging to the badnavirus group, occurring in pineapple plants. The relationship of the clostero-like and bacilliform viruses to yield loss and mealybug wilt in pineapples is unknown.
A previously undescribed sub-group 2 rhabdovirus was isolated in Queensland from Datura stramonium with symptoms of vein yellowing, leaf distortion and reduced leaf size. Particles accumulated in the perinuclear space of infected cells of D. stramonium and measured 77 x 166 nm in preparations from sap. The virus was named datura yellow vein virus (DYVV) and was graft-transmitted to several hosts in the Solanaceae including Lycopersicon esculentum, Nicotiana tabacum and Solanum melongena, but not to Capsicum annuum or Solanum tuberosum. DYVV was not transmitted by mechanical inoculation and no insect vector was found. Purified particles of DYVV contained four structural proteins with molecular weights of about 78, 47, 41 and 36 kd. The 78 kd protein bound the lectin concanavalin A, thus identifying it as the viral glycoprotein. DYVV was serologically distinct from 1 1 other rhabdoviruses belonging to both subgroups, including potato chlorotic stunt, potato yellow dwarf (2 isolates) and tomato vein yellowing viruses. The glycoprotein only of DYVV cross-reacted with a polyclonal antiserum to sonchus yellow net virus.
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