scholarly journals Development of real-time PCR using Minor Groove Binding probe to monitor the biological control agent Candida oleophila (strain O)

2005 ◽  
Vol 60 (1) ◽  
pp. 73-82 ◽  
Author(s):  
Sébastien Massart ◽  
Deborah De Clercq ◽  
Michel Salmon ◽  
Catherine Dickburt ◽  
M. Haissam Jijakli
2003 ◽  
Vol 69 (8) ◽  
pp. 4788-4793 ◽  
Author(s):  
S. D. Atkins ◽  
I. M. Clark ◽  
D. Sosnowska ◽  
P. R. Hirsch ◽  
B. R. Kerry

ABSTRACT Potato cyst nematodes (PCN) are serious pests in commercial potato production, causing yield losses valued at approximately $300 million in the European Community. The nematophagous fungus Plectosphaerella cucumerina has demonstrated its potential as a biological control agent against PCN populations by reducing field populations by up to 60% in trials. The use of biological control agents in the field requires the development of specific techniques to monitor the release, population size, spread or decline, and pathogenicity against its host. A range of methods have therefore been developed to monitor P. cucumerina. A species-specific PCR primer set (PcCF1-PcCR1) was designed that was able to detect the presence of P. cucumerina in soil, root, and nematode samples. PCR was combined with a bait method to identify P. cucumerina from infected nematode eggs, confirming the parasitic ability of the fungus. A selective medium was adapted to isolate the fungus from root and soil samples and was used to quantify the fungus from field sites. A second P. cucumerina-specific primer set (PcRTF1-PcRTR1) and a Taqman probe (PcRTP1) were designed for real-time PCR quantification of the fungus and provided a very sensitive means of detecting the fungus from soil. PCR, bait, and culture methods were combined to investigate the presence and abundance of P. cucumerina from two field sites in the United Kingdom where PCN populations were naturally declining. All methods enabled differences in the activity of P. cucumerina to be detected, and the results demonstrated the importance of using a combination of methods to investigate population size and activity of fungi.


2011 ◽  
Vol 91 (2) ◽  
pp. 243-245 ◽  
Author(s):  
Elena Galletti ◽  
Paolo Bonilauri ◽  
Lia Bardasi ◽  
Maria Cristina Fontana ◽  
Mattia Ramini ◽  
...  

2011 ◽  
Vol 322 (1) ◽  
pp. 34-40 ◽  
Author(s):  
Veronique Edel-Hermann ◽  
Sébastien Aimé ◽  
Christelle Cordier ◽  
Chantal Olivain ◽  
Christian Steinberg ◽  
...  

2007 ◽  
Vol 361 (1) ◽  
pp. 55-64 ◽  
Author(s):  
Jacob D. Durtschi ◽  
Jeffery Stevenson ◽  
Weston Hymas ◽  
Karl V. Voelkerding

2006 ◽  
Vol 72 (4) ◽  
pp. 2421-2427 ◽  
Author(s):  
Marta Pujol ◽  
Esther Badosa ◽  
Charles Manceau ◽  
Emilio Montesinos

ABSTRACT The colonization of apple blossoms and leaves by Pseudomonas fluorescens EPS62e was monitored in greenhouse and field trials using cultivable cell counting and real-time PCR. The real-time PCR provided a specific quantitative method for the detection of strain EPS62e. The detection level was around 102 cells g (fresh weight)−1 and the standard curve was linear within a 5-log range. EPS62e actively colonized flowers reaching values from 107 to 108 cells per blossom. In apple flowers, no significant differences were observed between population levels obtained by real-time PCR and plating, suggesting that viable but nonculturable (VBNC) cells and residual nondegraded DNA were not present. In contrast, on apple leaves, where cultivable populations of EPS62e decreased with time, significant differences were observed between real-time PCR and plating. These differences indicate the presence of VBNC cells or nondegraded DNA after cell death. Therefore, the EPS62e population was under optimal conditions during the colonization of flowers but it was stressed and poorly survived on leaves. It was concluded that for monitoring this biological control agent, the combined use of cultivable cell count and real-time PCR is necessary.


2012 ◽  
Vol 85 (2) ◽  
pp. 370-377 ◽  
Author(s):  
Zhifeng Li ◽  
Lunbiao Cui ◽  
Minghao Zhou ◽  
Xian Qi ◽  
Changjun Bao ◽  
...  

2019 ◽  
Vol 265 ◽  
pp. 9-14 ◽  
Author(s):  
David A. Sutton ◽  
David P. Allen ◽  
Chad M. Fuller ◽  
Jo Mayers ◽  
Benjamin C. Mollett ◽  
...  

2012 ◽  
Vol 181 (2) ◽  
pp. 148-154 ◽  
Author(s):  
Tao Yun ◽  
Zheng Ni ◽  
Jionggang Hua ◽  
Weicheng Ye ◽  
Liu Chen ◽  
...  

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