4.3 Article

Quantification of endophyte Serendipita indica in Brassica napus roots by qPCR

期刊

CROP & PASTURE SCIENCE
卷 72, 期 12, 页码 985-993

出版社

CSIRO PUBLISHING
DOI: 10.1071/CP21265

关键词

absolute quantification; inoculation concentration; inoculum density; molecular detection; plant-endophyte interaction; plant growth promotion; real-time PCR; symbiosis

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The study utilized qPCR to investigate the impact of inoculum concentrations on the root colonisation density of the fungal endophyte S. indica in Brassica napus. The results showed significant effects of inoculum concentration on colonisation density, while the percent root colonisation remained consistent across all treatments.
Context. The fungal endophyte Serendipita indica enhances plant growth and plant resistance to biotic and abiotic stresses. Inoculum concentration greatly impacts the endophyte-plant interaction from mutualism to antagonism. Aims and methods. We used both microscopy and qPCR to examine the effect of inoculum concentrations on the extent (%) and density of Brassica napus L. root colonisation by S. indica. B. napus seeds were inoculated with the fungus at five different inoculum concentrations (1-10% w/w basis). Key results. Standard curves were constructed using the mean threshold cycle (Ct) and serially diluted gDNA ranging between 4.14 x 10(2) and 2.65 x 10(5) colony forming units (CFU). The result indicated a linear relationship between Ct and the log of input DNA. Variation in inoculum concentration significantly affected the root colonisation density by the fungus shown by qPCR. However, the percent root colonisation (PRC) measure was not affected and remained the same across all the treatments. Conclusions. Our findings show that the qPCR assay developed will determine the colonisation density whereas PRC gives a measure of the incidence of infected roots. Also, we suggest that the optimum quantity of inoculum is a key factor for a successful interaction that impacts the plant-S. indica interaction. Implications To our knowledge, this is the first study that quantitative qPCR has been used to investigate the correlation between inoculum quantities and the corresponding density of root colonisation in S. indica.

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