Virus symptomatology in accessions of the Medicago truncatula core collection and identification of virus resistance phenotypes

2011 ◽  
Vol 62 (8) ◽  
pp. 686 ◽  
Author(s):  
M. Saqib ◽  
B. E. Gadja ◽  
M. G. K. Jones ◽  
R. A. C. Jones

Plants of 212 accessions from the core collection of model legume species Medicago truncatula were inoculated with infective sap containing Alfalfa mosaic virus (AMV, isolate EW), Bean yellow mosaic virus (BYMV, isolate MI) or Cucumber mosaic virus (CMV, isolate SN-1). A diverse range of systemic symptoms were obtained that varied widely in severity depending on the combination of virus isolate and accession, or, especially with AMV, some accessions became infected but did not display symptoms. The delay between virus inoculation and symptom appearance normally varied from 1 to 4 weeks, but with CMV it took up to 8 weeks in two accessions. Five (AMV), 59 (BYMV) and 22 (CMV) core accessions remained uninfected systemically. Plants of most of these accessions, and some that died or gave susceptible phenotypes, were then inoculated with two additional isolates of AMV (eight accessions), or two distinct strains of BYMV (58 accessions) and CMV (21 accessions). Plants of accession 11715 remained uninfected by CMV isolates CP (CMV subgroup 1) and LW (CMV subgroup 2), but those of all other previously uninfected accessions became infected systemically by all three viruses. All accessions inoculated with AMV isolates Aq and Hu, and most inoculated with BYMV isolate LKoj1-NN (generalist strain), BYMV isolate LP-1 (lupin strain), and CMV isolates CP and LW developed typical susceptible phenotypes. However, systemic hypersensitive phenotypes developed with BYMV LKoj1-NN and LP-1 in plants of 4456, or with LKoj1-NN only in 774, 1526, 4327, 14829, 15268, 22922 and 25654; 15268 and 25654 had developed this phenotype previously with MI (generalist strain). Similarly, plants of 21362 developed this phenotype with CMV CP and LW, while plants of 1526, 2748 and 31443 developed it with CP; 2748, 21632 and 31443 had developed it previously with SN-1 (mixture of subgroups 1 and 2). Once the genetic bases of the BYMV and CMV resistances found in M. truncatula are understood, they may prove useful in future virus resistance breeding among crop and pasture legumes.

Plant Disease ◽  
2012 ◽  
Vol 96 (9) ◽  
pp. 1384-1384 ◽  
Author(s):  
R. A. C. Jones ◽  
D. Real ◽  
S. J. Vincent ◽  
B. E. Gajda ◽  
B. A. Coutts

Tedera (Bituminaria bituminosa (L.) C.H. Stirton vars albomarginata and crassiuscula) is being established as a perennial pasture legume in southwest Australia because of its drought tolerance and ability to persist well during the dry summer and autumn period. Calico (bright yellow mosaic) leaf symptoms occurred on occasional tedera plants growing in genetic evaluation plots containing spaced plants at Newdegate in 2007 and Buntine in 2010. Alfalfa mosaic virus (AlMV) infection was suspected as it often causes calico in infected plants (1,2) and infects perennial pasture legumes in local pastures (1,3). Because AlMV frequently infects Medicago sativa (alfalfa) in Australia and its seed stocks are commonly infected (1,3), M. sativa buffer rows were likely sources for spread by aphids to healthy tedera plants. When leaf samples from plants with typical calico symptoms from Newdegate (2007) and Buntine (2010) were tested by ELISA using poyclonal antisera to AlMV, Bean yellow mosaic virus (BYMV) and Cucumber mosaic virus (CMV), only AlMV was detected. When leaf samples from 864 asymptomatic spaced plants belonging to 34 tedera accessions growing at Newdegate and Mount Barker in 2010 were tested by ELISA, no AlMV, BYMV, or CMV were detected, despite presence of M. sativa buffer rows. A culture of AlMV isolate EW was maintained by serial planting of infected seed of M. polymorpha L. (burr medic) and selecting seed-infected seedlings (1,3). Ten plants each of 61 accessions from the local tedera breeding program were grown at 20°C in an insect-proof air conditioned glasshouse. They were inoculated by rubbing leaves with infective sap containing AlMV-EW or healthy sap (five plants each) using Celite abrasive. Inoculations were always done two to three times to the same plants. When both inoculated and tip leaf samples from each plant were tested by ELISA, AlMV was detected in 52 of 305 AlMV-inoculated plants belonging to 36 of 61 accessions. Inoculated leaves developed local necrotic or chlorotic spots or blotches, or symptomless infection. Systemic invasion was detected in 20 plants from 12 accessions. Koch's postulates were fulfilled in 12 plants from nine accessions (1 to 2 of 5 plants each), obvious calico symptoms developing in uninoculated leaves, and AlMV being detected in symptomatic samples by ELISA, inoculation of sap to diagnostic indicator hosts (2) and RT-PCR with AlMV CP gene primers. Direct RT-PCR products were sequenced and lodged in GenBank. When complete nucleotide CP sequences (666 nt) of two isolates from symptomatic tedera samples and two from alfalfa (Aq-JX112758, Hu-JX112759) were compared with that of AlMV-EW, those from tedera and EW were identical (JX112757) but had 99.1 to 99.2% identities to the alfalfa isolates. JX112757 had 99.4% identity with Italian tomato isolate Y09110. Systemically infected tedera foliage sometimes also developed vein clearing, mosaic, necrotic spotting, leaf deformation, leaf downcurling, or chlorosis. Later-formed leaves sometimes recovered, but plant growth was often stunted. No infection was detected in the 305 plants inoculated with healthy sap. To our knowledge, this is the first report of AlMV infecting tedera in Australia or elsewhere. References: (1) B. A. Coutts and R. A. C. Jones. Ann. Appl. Biol. 140:37, 2002. (2) E. M. J. Jaspars and L. Bos. Association of Applied Biologists, Descriptions of Plant Viruses No. 229, 1980. (3) R. A. C. Jones. Aust. J. Agric. Res. 55:757, 2004.


1992 ◽  
Vol 43 (5) ◽  
pp. 1229 ◽  
Author(s):  
RAC Jones

Trials were done in 1988-90 to examine the effects of infection with three non persistently aphid-transmitted viruses on the productivity of manually inoculated spaced plants of annual pasture legumes growing in plots. Alfalfa mosaic virus (AMV) decreased herbage and root production (dry weights) of three subterranean clover (Trifolium subterraneum L.) cultivars by 20-49%. Cucumber mosaic virus (CMV) decreased herbage and root production of a murex medic (Medicago murex Wild.) cultivar by 78-90% and of two burr medic (M. polymorpha L.) cultivars by 56-82%. A mild isolate of bean yellow mosaic virus (BYMV) decreased herbage and root production of a subterranean clover cultivar by 31-40%, but with a severe isolate the corresponding losses were 60-63010 in the same cultivar and 79-80% in another. The severe BYMV isolate caused losses in herbage and root production of 38-61% in two burr medic cultivars. Seed yield losses recorded due to infection of subterranean clover were 71% with AMV and 58-76% with BYMV (severe isolate); both viruses decreased seed size as well as seed yield. CMV decreased seed yield by 94% in a burr medic cultivar; it also decreased seed size.


2021 ◽  
Vol 282 ◽  
pp. 110025
Author(s):  
Daniele Viana da Costa ◽  
Claudia Lougon de Almeida Paiva ◽  
Cíntia dos Santos Bento ◽  
Cláudia Pombo Sudré ◽  
Thâmara Figueiredo Menezes Cavalcanti ◽  
...  

2014 ◽  
Vol 13 (4) ◽  
pp. 9229-9243 ◽  
Author(s):  
M.M. Moulin ◽  
R. Rodrigues ◽  
S.F.F. Ribeiro ◽  
L.S.A. Gonçalves ◽  
C.S. Bento ◽  
...  

Genetika ◽  
2015 ◽  
Vol 47 (2) ◽  
pp. 651-663 ◽  
Author(s):  
Dragana Milosevic ◽  
Ivana Stankovic ◽  
Aleksandra Bulajic ◽  
Maja Ignjatov ◽  
Zorica Nikolic ◽  
...  

During 2009 and 2010, a survey was conducted in pepper crops to detect the possible presence of Pepper mild mottle virus (PMMoV) in Serbia. A total of 239 pepper samples from 39 crops at 26 localities were collected and analyzed for the presence of PMMoV, Cucumber mosaic virus (CMV), Potato virus Y (PVY), and Alfalfa mosaic virus (AMV), using DAS-ELISA test. Although it was detected in a small percentage, PMMoV could pose a threat to pepper production in Serbia due to its rapid seed-borne spread. Presence of PMMoV was confirmed by serological and biological detection, followed by conventional reverse transcription RT-PCR, using primers specific for the RNA-dependent RNA polymerase (RdRp) and the coat protein (CP) genes. Molecular identification confirmed that the Serbian isolates belong to PMMoV pathotypes P1,2 which do not break the resistance gene L3. Reconstructed phylogenetic tree confirmed the allocation of the Serbian isolates together with the majority of PMMoV isolates which belong to pathotypes P1,2. This study represents the first serological and molecular characterization of PMMoV infection of pepper in Serbia, and provides important data on the population structure. The obtained data could have great influence on pepper production in Serbia as well as future pepper resistance breeding in the country.


2019 ◽  
Vol 139 (1) ◽  
pp. 93-106 ◽  
Author(s):  
Fuminori Kobayashi ◽  
Hisayo Kojima ◽  
Tsuyoshi Tanaka ◽  
Mika Saito ◽  
Chikako Kiribuchi‐Otobe ◽  
...  

Euphytica ◽  
2016 ◽  
Vol 211 (1) ◽  
pp. 91-101 ◽  
Author(s):  
Jin Xiao ◽  
Xueluan Chen ◽  
Zhitian Xu ◽  
Jiao Guo ◽  
Zhenzhen Wu ◽  
...  

2016 ◽  
Vol 76 (1) ◽  
pp. 104
Author(s):  
K. K. Panigrahi ◽  
T. R. Das ◽  
B. Baisakh ◽  
A. Mohanty ◽  
J. Pradhan

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