1992
DOI: 10.1016/0378-1097(92)90145-e
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Detection and differentiation of Colletotrichum gloeosporioides isolates using PCR

Abstract: An oligonucleotide primer (CgInt), synthesised from the variable internally transcribed spacer (ITS) 1 region of ribosomal DNA (rDNA) of Collectotrichum gloeosporioides was used for PCR with primer ITS4 (from a conserved sequence of the rDNA) to amplify a 450-bp fragment from the 25 C. gloeosporioides isolates tested. This specific fragment was amplified from as little as 10 fg of fungal DNA. A similar sized fragment was amplified from DNA extracted from C. gloeosporioides-infected tomato tissue. RAPD analysis… Show more

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Cited by 75 publications
(95 citation statements)
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“…Later, it was identified via PCR with a specific primer (CgInt) in accordance with methodology described by Mills et al (1992).…”
Section: S R G Moraes Et Almentioning
confidence: 99%
“…Later, it was identified via PCR with a specific primer (CgInt) in accordance with methodology described by Mills et al (1992).…”
Section: S R G Moraes Et Almentioning
confidence: 99%
“…Bridge and Arora 1994; Edel, 1998 [6]; Levesque et al, 1994 [7]; White et al, 1990; [8]; Mills et al;1992 [9]; The ITS regions were looked at, because of the ready availability of the comparative sequences and also because of the success obtained with this approach in other plant pathogenic fungi. The other consideration was, Ganoderma on oil palm occurs as dikaryotic mycelium and basidiocarps that give rise to monokaryotic basidiospores.…”
Section: Ganoderma Boninense (Pat)mentioning
confidence: 99%
“…PCR amplification was used to identify isolates as C. gloeosporioides or C. acutatum using species-specific primers (18,27,13). The methodology used for PCR analysis was described by Adaskaveg & Hartin (1).…”
Section: Inoculum Productionmentioning
confidence: 99%