Four strains of sugarcane mosaic virus infecting cereals and other grasses in Australia

1973 ◽  
Vol 24 (4) ◽  
pp. 465 ◽  
Author(s):  
DS Teakle ◽  
NE Grylls

Viruses of the sugar-cane mosaic virus (SCMV)-type were isolated from 23 naturally infected species of Gramineae in Queensland, New South Wales, or the Northern Territory. The virus isolates were placed in four groups or strains on the basis of host reactions. Each strain was named after an important perennial host, viz. (1) Johnson grass (Sorgltum halepense), (2) sugar-cane (Saccharum officinaruin), (3) sabi grass (Urochloa mosambicensis), and (4) Queensland blue couch grass (Digitaria didactyla). The strains could be distinguished on the basis of mosaic or necrotic reactions in Yates NK220Y and Atlas sorghums, on abi!ity to cause systemic infection of Johnson grass or sugar-cane, or local infection of French bean (Phaseolus vulgaris cv. Bountiful). This ability of the sabi grass strain to infect a dicotyledonous host is previously unreported for any strain of SCMV . All four virus strains had a normal particle length of 736�17 nm, but the variability in particle length was greater for the sugar-cane and Queensland blue couch grass strains than for the other two. The Johnson grass strain was only distantly serologicaliy related to the sugar-cane, sabi grass, and Queensland blue couch strains, but the latter three were very closely related amongst themselves. Five aphid species, Aphis craccivora, A. gossypii, Macrosiphum euphorbiae, Rhopalosiphum maidis, and R. padi mere shown to transmit at least one strain of SCMV. A. craccicora and R. maidis were each able to transit all four strains. The Johnson grass strain of SCMV is the major strain infecting maize and sorghum crops in Australia. It was probably the cause of the maize ringspot mottle disease first observed in 1948 and of the mosaic and necrotic diseases of Sorghum almum first observed in 1960. These early records and its distinctive host reactions and serological properties make it unlikely that it is z recent introduction to Australia.

1972 ◽  
Vol 25 (4) ◽  
pp. 873
Author(s):  
DS Teakle ◽  
RF Moore

A "Jolmson grass" strain of sugar-cane mosaic virus commonly infects crops of sorghum in New South Wales and Queensland. Infected sorghum plants show one of two types of systemic reaction, either a systemic necrosis or a systemic mosaic. Type of reaction is controlled by a single dominant gene, the N gene. The N-genotypes condition the necrotic reaction, while nn conditions the mosaic reaction (Teakle et al. 1970).


1981 ◽  
Vol 32 (5) ◽  
pp. 741 ◽  
Author(s):  
DM Persley ◽  
IF Martin ◽  
RS Greber

Maize inbred lines, derived from both Australian and exotic sources, and used in a breeding programme at Kairi, Qld, were screened for resistance to a Johnson grass strain of sugarcane mosaic virus (SCMV-Jg). There was a good correlation between ratings made following manual inoculation in a glasshouse and those following exposure to natural field infection. Seven lines were highly resistant in both glasshouse and field ratings. A further nine lines showed an intermediate level of resistance following manual inoculation and developed from 0 to 7 % infection under field conditions when a susceptible line developed 99 % infection. Data obtained following the manual inoculation of plants in segregating generations of crosses between resistant KL 57 and susceptible KL 9 were consistent with resistance being controlled by a single dominant gene. Six lines (Pa 405, CI 44, Tx 601, Oh 07, Oh 7B, 38-11) that were used as sources of resistance to maize dwarf mosaic virus, strain A (MDMV-A) in the U.S.A. developed natural infection levels of less than 15% with SCMV-Jg. Only Pa 405 was highly resistant to manual inoculation. Four of 11 SCMV-Jg resistant lines were also highly resistant to manual inoculations with the sugarcane, Sabi grass and Queensland blue couch grass strains.


2008 ◽  
Vol 98 (11) ◽  
pp. 1233-1241 ◽  
Author(s):  
F. E. Gildow ◽  
D. A. Shah ◽  
W. M. Sackett ◽  
T. Butzler ◽  
B. A. Nault ◽  
...  

Cucumber mosaic virus (CMV) is a major component of the virus complex that has become more pronounced in snap bean in the midwestern and northeastern United States since 2001. Multiple-vector-transfer tests were done to estimate the CMV transmission efficiencies (p) of the main aphid species identified in commercial snap bean fields in New York and Pennsylvania. The four most efficient vectors (p > 0.05) were Aphis gossypii, A. glycines, Acyrthosiphon pisum, and Therioaphis trifolii, which were all significant species in the migratory aphid populations in snap bean. Moderately efficient vectors (0.01 < p < 0.04) were A. spiraecola, A. craccivora, Macrosiphum euphorbiae, and Rhopalosiphum maidis. Poor vectors (p < 0.01) included A. fabae, Nearctaphis bakeri, and Myzus persicae. Only one species, Sitobion avenae, failed to transmit CMV in replicated tests. Estimates of p were consistent between different clones of the same aphid species and among three different field isolates of CMV tested. Single-vector-transfer test results for a subset of the species supported those obtained via the multiple-vector-transfer approach. Our results are consistent with the notion that A. glycines is a major vector of recent CMV epidemics in snap bean, but that species is only one of several that are involved.


1968 ◽  
Vol 19 (5) ◽  
pp. 767 ◽  
Author(s):  
RH Taylor ◽  
RD Pares

Two isolates of maize dwarf mosaic virus originating from maize (MDMV(M)) and Johnson grass (MDMV(J)) were distantly related to an Australian and a Californian strain of sugar-cane mosaic virus (SMV). MDMV(M) was shown to be distantly related serologically to a Californian strain but not to an Ohio strain of MDMV; MDMV(J) was not shown to be related serologically to either the Californian or the Ohio strain of MDMV. MDMV(M), MDMV(J), and the Australian SMV produced similar symptoms on sweet corn (Zea mays var. saccharata (Sturtev)), which under glasshouse conditions included an initial necrotic phase not previously described for MDMV. The three isolates showed different characteristics when purified from sweet corn by an identical procedure. The yields of MDMV(M) and MDMV(J) were higher than that of SMV, and these two isolates produced strong zones in density gradients whereas SMV produced a very weak zone. The normal length of MDMV(M) was 773 ± 6.35 mµ and that of MDMV(J) 778 ± 6.35 mµ and the particles of both were uniform. By contrast the particles of SMV were very uneven in length; the most common length was 650–750 mµ, but many longer and shorter particles were observed.


1974 ◽  
Vol 25 (1) ◽  
pp. 99 ◽  
Author(s):  
LJ Penrose

Sugarcane mosaic virus is widely distributed in New South Wales. It was isolated from 10 species of plants. Twenty-seven native and introduced grass species were susceptible to SCMV by mechanical inoculation. Seventeen new hosts of SCMV were recorded. Of 20 virus isolates from eight host species, only one—from sugarcane—failed to infect Johnson grass. The principal reservoir for sugarcane mosaic virus was Johnson grass.


2017 ◽  
Vol 38 (SI 2 - 6th Conf EFPP 2002) ◽  
pp. 542-544
Author(s):  
R. Pokorný ◽  
M. Porubová

Under greenhouse conditions 12 maize hybrids derived from crosses of four resistant lines with several lines of different level of susceptibility were evaluated for resistance to Czech isolate of Sugarcane mosaic virus (SCMV). These hybrids were not fully resistant to isolate of SCMV, but the symptoms on their newly growing leaves usually developed 1 to 3 weeks later in comparison with particular susceptible line, the course of infection was significantly slower and rate of infection lower. As for mechanisms of resistance, the presence of SCMV was detected by ELISA in inoculated leaves both of resistant and susceptible lines, but virus was detected 7 days later in resistant line. Systemic infection developed only in susceptible lines. These results indicate restriction of viral long distance movement in the resistant line.


2021 ◽  
Vol 3 (1) ◽  
Author(s):  
Zhi-Yong Yan ◽  
Xiao-Jie Xu ◽  
Le Fang ◽  
Chao Geng ◽  
Yan-Ping Tian ◽  
...  

AbstractCoat protein (CP) is required for potyviruses to move and establish a systemic infection in plants. π-stackings formed by aromatic residues play critical roles in maintaining protein stability and functions. As we know, many aromatic residues located in the core region of potyvirus CPs are conserved. However, their roles in potyvirus infection remain largely unknown. Here, through analysis of the three-dimensional model of the tobacco vein banding mosaic virus (TVBMV; genus Potyvirus) CP, 16 aromatic residues were predicated to form π-stackings. The results of transient expression experiments demonstrated that deletion of any of these 16 aromatic residues reduced CP accumulation. Infectivity assays showed that deletion of any of these aromatic residues in the TVBMV infectious clone abolished cell-to-cell movement and reduced replication of the virus. Substitution of Y105 and Y147 individually with non-aromatic residues alanine or glycine reduced CP accumulation, virus replication, and abolished the ability of TVBMV to move intercellularly, while substitution of these two residues individually with aromatic residues phenylalanine or tryptophan, had no or little effect on CP accumulation and TVBMV systemic movement and replication. Similar results were obtained from the CP mutants of watermelon mosaic virus (WMV, genus Potyvirus). Taken together, our results demonstrate that multiple aromatic residues in CP are involved in potyvirus movement by forming π-stackings to maintain CP accumulation.


Plant Methods ◽  
2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Decai Tuo ◽  
Peng Zhou ◽  
Pu Yan ◽  
Hongguang Cui ◽  
Yang Liu ◽  
...  

Abstract Background Cassava is an important crop for food security and industry in the least-developed and developing countries. The completion of the cassava genome sequence and identification of large numbers of candidate genes by next-generation sequencing provide extensive resources for cassava molecular breeding and increase the need for rapid and efficient gene function analysis systems in cassava. Several plant virus-induced gene silencing (VIGS) systems have been developed as reverse genetic tools for rapid gene function analysis in cassava. However, these VIGS vectors could cause severe viral symptoms or inefficient gene silencing. Results In this study, we constructed agroinfection-compatible infectious cDNA clones of cassava common mosaic virus isolate CM (CsCMV-CM, genus Potexvirus, family Alphaflexiviridae) that causes systemic infection with mild symptoms in cassava. CsCMV-CM was then modified to a viral vector carrying the Nimble cloning frame, which facilitates the rapid and high-throughput cloning of silencing fragments into the viral genome. The CsCMV-based vector successfully silenced phytoene desaturase (PDS) and magnesium chelatase subunit I (ChlI) in different cassava varieties and Nicotiana benthamiana. The silencing of the ChlI gene could persist for more than two months. Conclusions This CsCMV-based VIGS system provides a new tool for rapid and efficient gene function studies in cassava.


Author(s):  
Roberto Alers-Velazquez ◽  
Sushant Khandekar ◽  
Clare Muller ◽  
Jennifer Boldt ◽  
Scott Leisner

AbstractLower temperatures delayed development of systemic symptoms by Cauliflower mosaic virus (CaMV) in two different plant hosts. However, lower temperature exposure increased CaMV nucleic acid levels in leaves of systemically-infected turnips. Furthermore, lower temperature altered the formation of aggregates formed by the CaMV major inclusion body (IB) protein, P6. Finally, lower temperature altered the architecture of the actin cytoskeleton. These data may suggest that lower temperatures alter the actin cytoskeleton, facilitating the formation of larger IBs that hold on to their internal virions more strongly than small ones, impairing virus particle release and causing a delay in systemic infection.


2002 ◽  
Vol 15 (10) ◽  
pp. 1050-1057 ◽  
Author(s):  
Yongzhong Li ◽  
Scott M. Leisner

The Cauliflower mosaic virus (CaMV) gene VI product (P6) is a multifunctional protein essential for viral propagation. It is likely that at least some of these functions require P6 self-association. The work described here was performed to confirm that P6 self-associates and to identify domains involved in this interaction. Yeast two-hybrid analyses indicated that full-length P6 self-associates and that this interaction is specific. Additional analyses indicated that at least four independent domains bind to full-length P6. When a central domain (termed domain D3) was removed, these interactions were abolished. However, this deleted P6 was able to bind to the full-length wild-type protein and to isolated domain D3. Viruses lacking domain D3 were incapable of producing a systemic infection. Isolated domain D3 was capable of binding to at least two of the other domains but was unable to self-associate. This suggests that domain D3 facilitates P6 self-association by binding to the other domains but not itself. The presence of multiple domains involved in P6 self-association may help explain the ability of this protein to form the intracellular inclusions characteristic of caulimoviruses.


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