کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3406778 | 1223593 | 2012 | 4 صفحه PDF | دانلود رایگان |

An assay was developed for the detection of Pineapple mealybug wilt associated virus-2 (PMWaV-2), an important factor in the etiology of mealybug wilt of pineapple. The assay combines reverse transcription of RNA isolated from pineapple with a specific and very sensitive, single, closed-tube nested polymerase chain reaction (PCR) to amplify a segment of the coat protein gene of the PMWaV-2. The outer primers were designed to anneal at higher temperatures than the nested primers to prevent primer competition in consecutive amplification reactions. To reduce potential competition further, the outer primers were used at one-thousandth the concentration of the nested primers. The specificity and sensitivity of this assay are much greater than PCR using only a single primer-pair. A TaqMan® probe was also designed for use in quantitative PCR to detect and quantify the PCR amplification products directly in a single-tube assay. The advantages of the single-tube assays using both conventional and quantitative PCR are reduced handling time and prevention of cross contamination compared to regular nested PCR in which the reactions are carried out in two separate tubes.
► A highly sensitive nested PCR assay performed in a single closed tube for detection of viruses in plants was developed.
► The specificity and sensitivity of this assay are much greater than PCR using only a single primer-pair.
► The assay combines reverse transcription of RNA with a specific and very sensitive, single, close-tube nested PCR.
► Higher annealing temperature and limiting amounts of the outer primers versus the inner primers is the basis of this assay.
► The single tube assay was quantitative by the inclusion of Taqman® probe.
Journal: Journal of Virological Methods - Volume 183, Issue 2, August 2012, Pages 215–218