Induction of resistance in tomato against buckeye rot (Phytophthora nicotianae var. parasitica)

2021 ◽  
Vol 101 (1) ◽  
pp. 31
Author(s):  
Adikshita Sharma ◽  
B. P. Shridhar ◽  
Amit Sharma ◽  
Monica Sharma
Diabetes ◽  
1992 ◽  
Vol 41 (12) ◽  
pp. 1533-1539 ◽  
Author(s):  
G. de la Rubia ◽  
F. J. Oliver ◽  
T. Inoguchi ◽  
G. L. King

2007 ◽  
Vol 97 (8) ◽  
pp. 958-963 ◽  
Author(s):  
G. C. Colburn ◽  
J. H. Graham

Phytophthora root rot of citrus in Florida is caused by Phytophthora nicotianae and P. palmivora. A naturally occurring isolate of P. nicotianae (Pn117) was characterized as hypovirulent on citrus roots. Pn117 infected and colonized fibrous roots, but caused significantly less disease than the virulent isolates P. nicotianae Pn198 and P. palmivora Pp99. Coincident inoculation of rootstock seedlings of Cleopatra mandarin (Citrus reticulata) or Swingle citrumelo (C. paradisi × Poncirus trifoliata) with the hypovirulent Pn117 and the virulent isolates Pn198 and Pp99 did not reduce the severity of disease caused by the virulent Phytophthora spp. When either rootstock was inoculated with the hypovirulent Pn117 for 3 days prior to inoculation with virulent isolates, preinoculated seedlings had significantly less disease and greater root weight compared with seedlings inoculated with the virulent isolates alone. Recovery of the different colony types of Phytophthora spp. from roots of sweet orange (C. sinensis) or Swingle citrumelo was evaluated on semiselective medium after sequential inoculations with the hypovirulent Pn117 and virulent Pp99. Pn117 was isolated from roots at the same level as the Pp99 at 3 days post inoculation. Preinoculation of Pn117 for 3 days followed by inoculation with Pp99 resulted in greater recovery of the hypovirulent isolate and lower recovery of the virulent compared with coincident inoculation.


Agronomy ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 656
Author(s):  
Jing Jin ◽  
Rui Shi ◽  
Ramsey Steven Lewis ◽  
Howard David Shew

Phytophthora nicotianae is a devastating oomycete plant pathogen with a wide host range. On tobacco, it causes black shank, a disease that can result in severe economic losses. Deployment of host resistance is one of the most effective means of controlling tobacco black shank, but adaptation to complete and partial resistance by P. nicotianae can limit the long-term effectiveness of the resistance. The molecular basis of adaptation to partial resistance is largely unknown. RNAseq was performed on two isolates of P. nicotianae (adapted to either the susceptible tobacco genotype Hicks or the partially resistant genotype K 326 Wz/Wz) to identify differentially expressed genes (DEGs) during their pathogenic interactions with K 326 Wz/Wz and Hicks. Approximately 69% of the up-regulated DEGs were associated with pathogenicity in the K 326 Wz/Wz-adapted isolate when sampled following infection of its adapted host K 326 Wz/Wz. Thirty-one percent of the up-regulated DEGs were associated with pathogenicity in the Hicks-adapted isolate on K 326 Wz/Wz. A broad spectrum of over-represented gene ontology (GO) terms were assigned to down-regulated genes in the Hicks-adapted isolate. In the host, a series of GO terms involved in nuclear biosynthesis processes were assigned to the down-regulated genes in K 326 Wz/Wz inoculated with K 326 Wz/Wz-adapted isolate. This study enhances our understanding of the molecular mechanisms of P. nicotianae adaptation to partial resistance in tobacco by elucidating how the pathogen recruits pathogenicity-associated genes that impact host biological activities.


2006 ◽  
Vol 115 (2) ◽  
pp. 263-267 ◽  
Author(s):  
A.-M. Kasselaki ◽  
M. W. Shaw ◽  
N. E. Malathrakis ◽  
J. Haralambous

2011 ◽  
Vol 115 (4-5) ◽  
pp. 432-442 ◽  
Author(s):  
Marco Antonio Mammella ◽  
Santa Olga Cacciola ◽  
Frank Martin ◽  
Leonardo Schena

1999 ◽  
Vol 11 (3) ◽  
pp. 229-242 ◽  
Author(s):  
Y. Gautam ◽  
D. M. Cahill ◽  
A. R. Hardham

Author(s):  
G. M. Waterhouse

Abstract A description is provided for Phytophthora nicotianae var. nicotianae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On Nicotiana plumbaginifolia, N. tabaci, N. spp., and on Amaranthus sp., Commelina benghalensis, C. nudiflora, Lycopersicon esculentum, Ricinus communis, Solanum melongena; also on wound inoculated Buxus sp., Daucus carota, Hedera helix, Ipomoea batatas and Trema amboensis. DISEASE: Black shank of tobacco. GEOGRAPHICAL DISTRIBUTION: Africa (Malawi, Mauritius, Uganda); Asia (Ceylon, China, Formosa, India, Indonesia, Japan, Java, Malaya, Philippines, Sumatra); Central America & West Indies (Cuba, Jamaica, Puerto Rico, Santo Domingo, Trinidad); Europe (Bulgaria, Germany, Greece, Italy, Poland, Romania, U.S.S.R.); North America (U.S.A.); South America (Brazil, Colombia, Venezuela). TRANSMISSION: Soil-borne, persisting in soil for at least 4 years between tobacco crops, and not eliminated by a 3 year rotation or a 4 year fallow (41: 409; 39: 126). Tobacco leaves have been used to indicate disease potential in infested soil after serial dilution with sterile soil (42: 408). Spread in contaminated pond water used in overhead irrigation also suspected (43, 1413). Wind-borne spread up to 800 ft. has been recorded (39: 500).


Author(s):  
G. M. Waterhouse

Abstract A description is provided for Phytophthora nicotianae var. parasitica. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a very wide range of host plants comprising 58 families including: avocado, castor, Cinchona spp., citrus, cotton, eggplant, guava, lucerne, papaw, parsley, pineapple, Piper betle, rhubarb, sesame, strawberry, tomato. DISEASES: Damping-off of seedlings (tomato, castor, citrus, cotton); root rot (citrus, avocado, strawberry, lucerne); crown rot (parsley, rhubarb, strawberry, lucerne); brown stem rot of tobacco; stem canker and tip blight of Cinchona spp. ; leaf blight (castor, sesame, pineapple, Piper betle) and fruit rot (citrus, tomato, guava, papaw, eggplant). GEOGRAPHICAL DISTRIBUTION: Africa (Ethiopia, Mali, Madagascar, Mauritius, Morocco, Nigeria, Sierra Leone, Southern Rhodesia, Tanganyika); Asia (Burma, Ceylon, China, Formosa, India, Israel, Japan, Java, Malaya, Philippines); Australia & Oceania (Australia, Hawaii, Tasmania); Europe (Cyprus, France, Germany, Great Britain, Holland, Ireland, Italy, Poland, Portugal, U.S.S.R.); North America (Bermuda, Canada, Mexico, U.S.A.); Central America & West Indies (Costa Rica, Cuba, El Salvador, Guatemala, Jamaica, Montserrat, Puerto Rico, Trinidad);. South America (Argentina, Brazil, British Guiana, Colombia, Paraguay, Peru, Venezuela). TRANSMISSION: Soil-borne, spreading rapidly after heavy rain or where soil remains moist or water-logged (40: 470). Also recorded in drainage water in India and in reservoirs and canals supplying citrus groves in U.S.A. (23: 45; 39: 24). A method for determining a disease potential index in soil using lemon fruit has been described (38: 4). Also present in testas of seeds from diseased citrus fruit which may infect nursery seedbeds (37: 165).


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