Identification of new resistant sources for bacterial blight in pomegranate

被引:10
作者
Priya, B. Tanuja [1 ,3 ]
Murthy, B. N. S. [1 ]
Gopalakrishnan, C. [2 ]
Artal, Rashmi B. [2 ]
Jagannath, S. [3 ]
机构
[1] IIHR, Div Fruit Sci, Bengaluru 560089, India
[2] IIHR, Div Plant Pathol, Bengaluru 560089, India
[3] Univ Hort Sci, Div Fruit Sci, Coll Hort, Bengaluru, India
关键词
Pomegranate; Bacterial blight; Xanthomonas axonopodis pv. punicae; Resistant source; Germplasm; USDA; India; AXONOPODIS PV. PUNICAE; ANTIOXIDANT CAPACITY; XANTHOMONAS; STRAINS; STOMATA;
D O I
10.1007/s10658-016-0947-1
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Bacterial blight is a highly devastating disease caused by Xanthomonas axonopodis pv. punicae, recording 60 to 80 percent yield-loss of pomegranate in India. In the present investigation, a total of 209 genotypes including 105 exotic types from USDA, 66 wild types and 38 cultivated types from India were screened and categorized into fifteen clusters using cluster and principal component analysis. Genotypes of cluster 15, viz. 108 B and 99 A from USDA and 318734, Daru-18 and IIHR-30 from India, were found to be resistant to bacterial blight while genotypes of cluster 9 were highly susceptible. Two genotypes, each from cluster 15 (318734) and 9 (Ruby), were compared for biochemical and histological parameters to understand the defense mechanism. Significantly, higher accumulation of defense related metabolites, viz. total phenol, flavonoid and antioxidant contents, were observed in resistant genotype (318734). Fewer numbers of stomatal pores that served as portals of entry for plant pathogens were recorded in this genotype. Resistance observed in genotype 318734 might be due to an incompatible interaction between host and pathogen compared to other genotypes. This is the first report of putative resistance sources in pomegranate against Xanthomonas axonopodis pv. punicae.
引用
收藏
页码:609 / 624
页数:16
相关论文
共 49 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]  
[Anonymous], 2014, AREA PRODUCTION
[3]  
Ashry N. A., 2011, World Journal of Agricultural Sciences, V7, P78
[4]  
Benagi VI, 2009, 2 ITNS POM MIN INCL, P53, DOI [10.17660/ActaHortic.2011.890.66, DOI 10.17660/ACTAHORTIC.2011.890.66]
[5]   The ferric reducing ability of plasma (FRAP) as a measure of ''antioxidant power'': The FRAP assay [J].
Benzie, IFF ;
Strain, JJ .
ANALYTICAL BIOCHEMISTRY, 1996, 239 (01) :70-76
[6]   Comparison of leaf disk, greenhouse, and field screening procedures for evaluation of grape seedlings for downy mildew resistance [J].
Brown, MV ;
Moore, JN ;
Fenn, P ;
McNew, RW .
HORTSCIENCE, 1999, 34 (02) :331-333
[7]  
Chand Ramesh, 1993, International Journal of Tropical Plant Diseases, V11, P85
[8]   Contribution of individual polyphenolics to total antioxidant capacity of plums [J].
Chun, OK ;
Kim, DO ;
Moon, HY ;
Kang, HG ;
Lee, CY .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (25) :7240-7245
[9]   Impact of 16S rRNA gene sequence analysis for identification of bacteria on clinical microbiology and infectious diseases [J].
Clarridge, JE .
CLINICAL MICROBIOLOGY REVIEWS, 2004, 17 (04) :840-+
[10]  
Ensikat H.J., 2010, MICROSCOPY SCI TECHN, P248