Occurrence of cucumber green mottle mosaic virus in Western Australia

Author(s):  
Monica A. Kehoe ◽  
Craig Webster ◽  
Cuiping Wang ◽  
Roger A. C. Jones ◽  
Brenda A. Coutts
2005 ◽  
Vol 54 (4) ◽  
pp. 563-563 ◽  
Author(s):  
M. Saqib ◽  
R. A. C. Jones ◽  
B. Cayford ◽  
M. G. K. Jones

1982 ◽  
Vol 1 (4) ◽  
pp. 491-496 ◽  
Author(s):  
G.D. McLean ◽  
J.R. Burt ◽  
D.W. Thomas ◽  
A.N. Sproul

Author(s):  

Abstract A new distribution map is provided for Dahlia mosaic virus Brierly. Hosts: on Dahlia spp. Information is given on the geographical distribution in AFRICA, Madagascar, Malawi, South Africa, Tanzania (Wallace) Zambia, Zimbabwe, ASIA, China, Taiwan, AUSTRALASIA, Australia, Western Australia, Tasmania, EUROPE, Belgium, Britain (Dennis & Foister; Moore), Czechoslovakia, Denmark, France, Germany, Greece, Italy, Romania, Sweden, NORTH AMERICA, Canada, USA, SOUTH AMERICA, Argentina, Brazil (Minas Gerais).


Plant Disease ◽  
2014 ◽  
Vol 98 (2) ◽  
pp. 285-285 ◽  
Author(s):  
B. A. Coutts ◽  
B. A. Cox ◽  
G. J. Thomas ◽  
R. A. C. Jones

In eastern Australia, there have been several as yet unconfirmed reports of Wheat mosaic virus (WMoV) infecting wheat (3). WMoV, previously known as High plains virus (HPV), is transmitted by the wheat curl mite (WCM, Aceria tosichella). It is often found in mixed infections with Wheat streak mosaic virus (WSMV), also transmitted by WCM (2,3). WSMV was first identified in Australia in 2003 (3). In October 2012, stunted wheat plants with severe yellow leaf streaking were common in a field experiment near Corrigin in Western Australia consisting of nine wheat cultivars. These symptoms were also common in two commercial crops of wheat cv. Mace near Kulin. Leaf samples (one per plant) from each location were tested by ELISA using specific antiserum to WMoV (syn. HPV 17200, Agdia, Elkhart, IN). At the field experiment, 20 leaf samples were collected at random from each wheat plot (4 replicates) and tested individually by ELISA. WMoV incidence was 5% for cv. Yipti, 16% for cvs Emu Rock, Wyalkatchem and Mace, 22% for cvs. Corack, Fortune, Calingiri, and Magenta, and 55% for cv. Cobra. From the two commercial wheat crops, 100 leaf samples were collected at random from each and tested by ELISA. WMoV incidence was 2 and 4%. In addition, 50 leaf samples of Hordeum leporinum (barley grass) and 20 of Lolium rigidum (annual ryegrass) were collected and tested by ELISA. WMoV incidence was 2% in H. leporinum, but 0% in L. rigidum. Infected H. leporinum plants were symptomless. Symptomatic wheat leaf samples from both sites were tested by RT-PCR using WMoV specific primers designed from its RNA3 sequence (1). The PCR products (339 bp) were sequenced and lodged in GenBank (Accession Nos KC337341 and KC337342). WMoV isolates from Corrigin (WA-CG12) and Kulin (WA-KU12) had identical sequences. When the nucleic acid sequences of WA-CG12 and WA-KU12 were compared with those of the three other WMoV isolates on GenBank, they had 100% nucleotide sequence identity with a Nebraska isolate (U60141), and 99.7% identity to two United States sweet corn isolates (AY836524 and AY836525). Ten symptomatic wheat plants were collected from each location, transplanted into pots and leaf samples tested individually for WMoV and WSMV (07048, Loewe, Germany) by ELISA. All were infected with both viruses and infested with WCM. WCM-infested glumes (>10 WCM/glume) were placed on the leaf sheaths of 60 wheat plants cv. Calingiri (35 with WA-CG12 and 25 with WA-KU12) and 13 sweet corn plants cv. Snow Gold (WA-CG12 only). In addition, 20 wheat and 10 sweet corn plants were left without infested glumes to be uninoculated controls. All 60 WCM-inoculated wheat plants became stunted with severe leaf streaking. When leaf samples from each plant were tested by ELISA 18 to 30 days later, both viruses were detected. WMoV was detected in all 13 WCM-inoculated sweet corn plants and WSMV in two of them. Plants with WMoV alone initially had short chlorotic leaf streaks that subsequently combined, causing broad streaks. These are typical WMoV symptoms for sweet corn (1). No symptoms developed and no virus was detected in any of the uninoculated wheat or sweet corn control plants. The WMoV nucleotide sequence obtained from an infected sweet corn plant was identical to those of WA-CG12 and WA-KU12. To our knowledge, this is the first confirmed report of WMoV presence in Australia. References: (1) B. S. M. Lebas et al. Plant Dis. 89:1103, 2005. (2) D. Navia et al. Exp. Appl. Acarol. 59:95, 2013. (3) J. M. Skare et al. Virology 347:343, 2006.


1994 ◽  
Vol 45 (1) ◽  
pp. 183 ◽  
Author(s):  
SJ McKirdy ◽  
BA Coutts ◽  
RAC Jones

In 1990, infection with bean yellow mosaic virus (BYMV) was widespread in subterranean clover (Trifolium subterraneum) pastures in the south-west of Western Australia. When 100 leaves were sampled at random per pasture, the virus was detected by ELISA in 23 of 87 pastures and incidences of infection ranged from 1 to 64%. BYMV was present in all seven districts surveyed, but highest incidences of infection occurred in the Busselton district. In smaller surveys in 1989 and 1992, incidences of infection in pastures were higher than in 1990, and ranged up to 90%. In 1992, when petals from 1703 samples of 59 species of perennial native legumes from 117 sites were tested by ELISA, only 1% were found infected with BYMV. The infected samples came from 5/7 districts surveyed. Species found infected were Kennedia prostrata, K. coccinea, Hovea elliptica and H. pungens. Representative isolates of BYMV from subterranean clover and native legumes did not infect white clover systemically confirming that clover yellow vein virus (CYVV) was not involved. It was concluded that BYMV infection was present in many subterranean clover pastures, but normally at low incidences, except in epidemic years such as 1992. Also, perennial native legumes are unlikely to act as major reservoirs for reinfection of annual pastures each year. In areas of Australia with Mediterranean climates where perennial pastures are absent, persistence of the virus over summer is therefore by some other method than infection of perennials.


2005 ◽  
Vol 56 (8) ◽  
pp. 847 ◽  
Author(s):  
B. A. Coutts ◽  
R. A. C. Jones

During 2003–04, a survey was done to determine the incidence and distribution of virus diseases infecting cucurbit crops growing in the field at Kununurra, Broome, and Carnarvon in north-western Australia, Perth in south-western Australia, and Darwin and Katherine in the Northern Territory. Overall, 43 cucurbit-growing farms and 172 crops of susceptible cultivars were sampled. From each crop, shoot samples were collected from plants chosen at random and from symptomatic plants. Shoot samples were sometimes also collected from potential alternative virus hosts (cucurbit volunteer plants and weeds). All samples were tested by enzyme-linked immunosorbent assay (ELISA) using antibodies to Cucumber mosaic virus (CMV), Papaya ringspot virus-cucurbit strain (PRSV), Squash mosaic virus (SqMV), Watermelon mosaic virus (WMV), and Zucchini yellow mosaic virus (ZYMV). Samples from one-third of the crops were also tested by tissue blot immunosorbent assay (TBIA) using generic luteovirus antibodies. Overall, 72% of farms and 56% of crops sampled were virus-infected. The growing areas with the highest incidences of virus infection were Darwin and Carnarvon, and those with the lowest incidences were Katherine and Perth. For WA, overall 78% of farms and 56% of crops were virus-infected, and in the NT the corresponding figures were 55% of farms and 54% of crops. Overall virus incidences in individual crops sometimes reached 100% infection. Crops of cucumber, melon, pumpkin, squash, and zucchini were all infected, with squash and zucchini being the most severely affected. The most prevalent viruses were ZYMV and PRSV, each being detected in 5 and 4 of 6 cucurbit-growing areas, respectively, with infected crop incidences of <1–100%. SqMV was detected in 2 cucurbit-growing areas, sometimes reaching high incidences (<1–60%). WMV and CMV were found in 3 and 4 of 6 cucurbit-growing areas, respectively, but generally at low incidences in infected crops (<1–8%). Infection with luteovirus was found in 3 growing areas but only occurred in 16% of crops. Beet western yellows virus was detected once but at least one other luteovirus was also present. Infection of individual crops by more than 1 virus was common, with up to 4 viruses found within the same crop. Virus-resistant pumpkin cultivars (6 crops) had little infection when adjacent virus-susceptible cucurbit crops had high virus incidences. Viruses were detected in cucurbit volunteer plants and weeds, suggesting that they may act as important reservoirs for spread to nearby cucurbit crops. In general, established cucurbit-growing farms in close proximity to others and with poor crop hygiene suffered most from virus epidemics, whereas isolated farms with large-sized crops or that had only recently started growing cucurbits had less infection. The extent of infection revealed in this survey, and the financial losses to growers resulting from virus-induced yield losses and high fruit rejection rates, are cause for concern for the Australian cucurbit industry.


1995 ◽  
Vol 35 (6) ◽  
pp. 745
Author(s):  
HL Tapscott ◽  
WA Cowling

The growth and yield of 97 seedlots of Gungurm narrow-leafed lupins (Lupinus angustifolius L.) from Western Australia were assessed to identify geographical source or nutritional and physical parameters in the seed that can be used to predict the yield potential of a seedlot. Seedlots were obtained from the 1990 harvest on farms in the south-western cropping region of Western Australia, with up to 7 seedlots from each of 14 crop variety recommendation areas. Each seed lot was assessed for seed size (mean 144 mg), germination percentage (mean 87%), cucumber mosaic virus seed infection (mean 0.11%), and several seed nutrients. Seedlots were sown at 100 kg/ha (without adjusting for germination or seed size) at 4 sites in Western Australia in 1991. Plant density, shoot dry weight (at 6 weeks), and grain yield varied significantly among seedlots, with average grain yield ranging from 951 to 1478 kg/ha (l.s.d. = 240 kg/ha at P = 0.05). Seed size influenced (P<0.001) stand density (r = -0.33) and shoot dry weight (r = 0.58) but not grain yield (r = 0.09, n.s.). No seed nutrient was more than weakly associated with grain yield, nor was there an association of seedlot yield with geographical source of seed. High germination percentage and low cucumber mosaic virus infection were the main predictors of high grain yield in this experiment, but accounted for only 40% of the yield variance among seedlots.


Sign in / Sign up

Export Citation Format

Share Document