[Objectives]This study was conducted to clarify the pathogens causing suspected sugarcane leaf scald symptoms in sugarcane plants found in the Xinping sugarcane area of Yunnan in 2019.[Methods]The XAF1/XAR1 specific p...[Objectives]This study was conducted to clarify the pathogens causing suspected sugarcane leaf scald symptoms in sugarcane plants found in the Xinping sugarcane area of Yunnan in 2019.[Methods]The XAF1/XAR1 specific primers of Xanthomonas albilineans were used to detect 8 suspected samples from Xinping County,Yunnan Province.[Results]The specific band 600 bp in size was detected.The sequencing results showed that the sequences detected were all 608 bp,and were 100%identical.The BLAST search results showed that the obtained sequence was 100%identical to the nucleotide sequence of X.albilineans GPE PC73 strain(GenBank accession number:FP565176)from France,and they were located in the same branch of the phylogenetic tree.According to the field symptom diagnosis and molecular identification results,the sugarcane disease in Xinping,Yunnan was confirmed to be the quarantine disease sugarcane leaf scald caused by X.allbilineasn.[Conclusions]The pathogens were identified by molecular biological identification methods,providing a scientific basis for the prevention and control of leaf scald disease in the future.展开更多
Leaf discs of five cultivars of sugarcane exhibiting different degree of susceptibility to leaf scald were used to measure β-1,3 glucanase activity before and after experimental infection with Xanthomonas albilineans...Leaf discs of five cultivars of sugarcane exhibiting different degree of susceptibility to leaf scald were used to measure β-1,3 glucanase activity before and after experimental infection with Xanthomonas albilineans. Leaf discs were permeabilized with iso-propanol to facilitate the uptake of the enzyme substrate by intact tissues and to improve the enzyme assay. Bacterial infection significantly enhances β-1,3 glucanase activity of sensitive cultivars whereas significantly decreased that of the resistant one. Low concentrations of salicylate increase the hydrolase activity whereas jasmonic acid do not act as an elicitor of the enzyme and β-1,3 glucanase, such as laminarin, significantly inhibits the production of β-1,3 glucanase. Thus, the enzyme must be considered as a sensitivity factor induced by the pathogen.展开更多
基金Special Fund for Construction of Sugar Crop Research System(CARS-170303)Yunling Industrial Technology Leading Talent Training Project:Sugarcane Pest Control(2018LJRC56)Special Fund for the Construction of Modern Agricultural Industry Technology System in Yunnan Province.
文摘[Objectives]This study was conducted to clarify the pathogens causing suspected sugarcane leaf scald symptoms in sugarcane plants found in the Xinping sugarcane area of Yunnan in 2019.[Methods]The XAF1/XAR1 specific primers of Xanthomonas albilineans were used to detect 8 suspected samples from Xinping County,Yunnan Province.[Results]The specific band 600 bp in size was detected.The sequencing results showed that the sequences detected were all 608 bp,and were 100%identical.The BLAST search results showed that the obtained sequence was 100%identical to the nucleotide sequence of X.albilineans GPE PC73 strain(GenBank accession number:FP565176)from France,and they were located in the same branch of the phylogenetic tree.According to the field symptom diagnosis and molecular identification results,the sugarcane disease in Xinping,Yunnan was confirmed to be the quarantine disease sugarcane leaf scald caused by X.allbilineasn.[Conclusions]The pathogens were identified by molecular biological identification methods,providing a scientific basis for the prevention and control of leaf scald disease in the future.
文摘Leaf discs of five cultivars of sugarcane exhibiting different degree of susceptibility to leaf scald were used to measure β-1,3 glucanase activity before and after experimental infection with Xanthomonas albilineans. Leaf discs were permeabilized with iso-propanol to facilitate the uptake of the enzyme substrate by intact tissues and to improve the enzyme assay. Bacterial infection significantly enhances β-1,3 glucanase activity of sensitive cultivars whereas significantly decreased that of the resistant one. Low concentrations of salicylate increase the hydrolase activity whereas jasmonic acid do not act as an elicitor of the enzyme and β-1,3 glucanase, such as laminarin, significantly inhibits the production of β-1,3 glucanase. Thus, the enzyme must be considered as a sensitivity factor induced by the pathogen.
