Hardenbergia mosaic virus: Crossing the barrier between native and introduced plant species

2014 ◽  
Vol 184 ◽  
pp. 87-92 ◽  
Author(s):  
M.A. Kehoe ◽  
B.A. Coutts ◽  
B.J. Buirchell ◽  
R.A.C. Jones
Plant Disease ◽  
2006 ◽  
Vol 90 (6) ◽  
pp. 833-833 ◽  
Author(s):  
C. A. Baker ◽  
L. Breman ◽  
L. Jones

In the fall of 1998, the Division of Plant Industry (DPI) received vegetative propagations of Scutellaria longifolia (skullcap) with symptoms of foliar mosaic, chlorotic/necrotic ringspots, and wavy line patterns from a nursery in Manatee County. Flexuous particles approximately 500 nm long were found with electron microscopy. The plants tested positive for Papaya mosaic virus (PaMV) in an enzyme-linked immunosorbent assay (ELISA) test with antiserum to PaMV (Agdia, Elkhart, IN). However, in immunodiffusion tests (antiserum from D. Purcifull, University of Florida), this virus gave a reaction of partial identity indicating it was related but not identical to PaMV (1). The original infected plants were kept in a greenhouse. In January 2005, a specimen of Crossandra infundibuliformis (firecracker plant) with mosaic symptoms was submitted to the DPI from a nursery in Alachua County. Inclusions found with light microscopy and particles found with electron microscopy indicated that this plant was infected with a potexvirus. This was confirmed by reverse transcription-polymerase chain reaction (RT-PCR) with primers designed to detect members of the virus family Potexviridae (3). These plants reacted positive to PaMV antiserum in ELISA and gave a reaction of partial identity to PaMV in immunodiffusion. A specimen of Portulaca grandiflora (moss rose) with distorted leaves found at a local retail store was also tested and gave the same results. Leaves from each of the three plant species were rubbed onto a set of indicator plants using Carborundum and potassium phosphate buffer. Total RNA was extracted from symptomatic indicator plants of Nicotiana benthamiana. RT-PCR (3) was performed, and PCR products were sequenced directly. Sequences of approximately 700 bp were obtained for all three plant species and showed 98% identity with each other. BLAST search results showed that these sequences were 93% identical to an Alternanthera mosaic virus (AltMV) sequence at the nucleotide level but only 76% identical to PaMV. The amino acid sequences were 98 and 82% identical to AltMV and PaMV, respectively. The PCR products of the virus from Scutellaria sp. were cloned, resequenced, and the sequence was entered into the GenBank (Accession No. DQ393785). The bioassay results matched those found for AltMV in Australia (2) and the northeastern United States (4), except that the Florida viruses infected Datura stramonium and Digitalis purpurea (foxglove). The virus associated with the symptoms of these three plants appears to be AltMV and not PaMV. AltMV has been found in ornamental plants in Australia, Italy, and the United States (Pennsylvania, Maryland, and now Florida). Since this virus is known to infect several plants asymptomatically and can be easily confused with PaMV serologically, it is likely that the distribution of this virus is much wider than is known at this time. References: (1) L. L. Breman. Plant Pathology Circular No. 396. Fla. Dept. Agric. Consum. Serv. DPI, 1999. (2) A. D. W. Geering and J. E. Thomas. Arch Virol 144:577, 1999. (3) A. Gibbs et al. J Virol Methods 74:67, 1998. (4) J. Hammond et al. Arch Virol. 151:477, 2006.


Plant Disease ◽  
2010 ◽  
Vol 94 (9) ◽  
pp. 1125-1131 ◽  
Author(s):  
Dallas L. Seifers ◽  
T. J. Martin ◽  
J. P. Fellers

Triticum mosaic virus (TriMV) is a newly discovered virus isolated from wheat (Triticum aestivum). This study was conducted to determine an experimental host range for TriMV and identify species that could serve as differential hosts for isolating TriMV from Wheat streak mosaic virus (WSMV). Plants tested were mechanically inoculated with the 06-123 isolate of TriMV or the Sidney 81 isolate of WSMV. Some plants were analyzed by enzyme-linked immunosorbent assay (ELISA) using antibodies of TriMV and WSMV. Plants infected with TriMV always produced mosaic symptoms and only extracts of symptomatic plants reacted with antibodies of TriMV. Maize is not a host for TriMV but barley, oat, rye, and triticale are hosts of TriMV. Certain barley and triticale accessions are hosts for TriMV but not WSMV. These plants can be used in combination with maize to separate WSMV and TriMV in plants infected by both viruses. We also showed that 8 wild grass species were susceptible to TriMV and 25 were not. All of the grasses susceptible to infection with TriMV have been reported as susceptible to infection with WSMV. Because of their growth habits, these plant species would be less desirable for use as differential hosts than maize, barley, and triticale.


2016 ◽  
Author(s):  
S. Ambrós ◽  
F. Martínez ◽  
P. Ivars ◽  
C. Hernández ◽  
F. de la Iglesia ◽  
...  

AbstractTomato is known to be a natural and experimental reservoir host for many plant viruses. In the last few years a new tobamovirus species, Tomato mottle mosaic virus (ToMMV), has been described infecting tomato and pepper plants in several countries worldwide. Upon observation of symptoms in tomato plants growing in a greenhouse in Valencia, Spain, we aimed to ascertain the etiology of the disease. Using standard molecular techniques, we first detected a positive sense single-stranded RNA virus as the probable causal agent. Next, we amplified, cloned and sequenced a ~3 kb fragment of its RNA genome which allowed us to identify the virus as a new ToMMV isolate. Through extensive assays on distinct plant species, we validated Koch’s postulates and investigated the host range of the ToMMV isolate. Several plant species were locally and/or systemically infected by the virus, some of which had not been previously reported as ToMMV hosts despite they are commonly used in research greenhouses. Finally, two reliable molecular diagnostic techniques were developed and used to assess the presence of ToMMV in different plants species. We discuss the possibility that, given the high sequence homology between ToMMV and Tomato mosaic virus, the former may have been mistakenly diagnosed as the latter by serological methods.


1969 ◽  
Vol 57 (1) ◽  
pp. 56-64
Author(s):  
J. Enrique Pérez ◽  
Julio Bird

A mosaic virus of Vigna hosei (Craib) Back is described. The virus was transmitted by mechanical means to several varieties or selections of Phaseolus vulgaris and to Cassia occidentalis and P. lathyroides. It was transmitted to seven different plant species by means of Aphis craccivora. It resembled somewhat the mosaic virus of V. repens on the basis of symptoms produced on several bean varieties and selections.


Oryx ◽  
1993 ◽  
Vol 27 (1) ◽  
pp. 22-26 ◽  
Author(s):  
Justin Gerlach

The Seychelles are the only high oceanic islands of granitic origin and their native vegetation is thus of considerable botanical interest. In the nineteenth and early twentieth centuries widespread clearance for coconut and cinnamon plantations resulted in native forest being confined mainly to montane areas. Cinnamon has proved to be very invasive in natural forest and a number of other introduced plant species have also been recognized as problematic for some time. Recent studies have revealed that two more introduced plant species - Memecylon floribunda and Clidemia hirta - are significant new threats to native vegetation on Mahe and Silhouette, respectively.


1992 ◽  
Vol 43 (3) ◽  
pp. 465 ◽  
Author(s):  
WS Wahyuni ◽  
RIB Francki

The symptoms and host ranges of 16 strains of cucumber mosaic virus (CMV) from both Subgroup I and II were compared on selected pasture and grain legumes. None infected either Arachis hypogea or Glycine max, although 13 other plant species were infected. The observation that success of inoculation varied with the time of year, may limit the usefulness of the biological differentiation of strains. No hosts tested distinguished Subgroup I or II isolates. The distribution of symptoms and virus in Medicago spp. was uneven and the virus was first detected in some cultivars 6-12 weeks after inoculation, indicating that any test for resistance to CMV in these species would have to be prolonged. Most cultivars of lupin tested were severely affected by several strains of CMV, which caused necrosis and death under conditions which excluded other pathogens.


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