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PCR‐based detection of Colletotrichum acutatum on strawberry

SREENIVASAPRASAD, S., SHARADA, K., BROWN, A. E., MILLS, P. R.·1996·Plant Pathology

Abstract

An oligonucleotide primer ( Ca Int 2) was synthesized from the variable internal transcribed spacer (ITS) 1 region of ribosomal DNA (rDNA) from Colletotrichum acutatum . PCR with primers Ca Int2 and ITS4 (from a conserved sequence of the rDNA) amplified a 490 bp fragment from several isolates of C. acutatum but not from other members of the genus Colletotrichum . Amplification of this fragment was achieved from 100 fg of fungal DNA. These primers amplified a fragment of the same size from DNA extracted from strawberry tissues infected by C. acutatum . Southern hybridization analysis confirmed the 490 bp fragment from C. acutatum DNA and infected strawberry to be identical. The species‐specific primer ( Ca Int2) developed in this work could be used for the accurate identification of C. acutatum and its detection on other host plants.

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Crossref · 10.1046/j.1365-3059.1996.d01-3.x

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Metadata

Authors
SREENIVASAPRASAD, S., SHARADA, K., BROWN, A. E., & MILLS, P. R.
Venue
Plant Pathology
Publisher
Wiley
Published
1996-08
Volume
45
Issue
4
Pages
650-655
ISSN
  • 0032-0862 (ISSN-L)
  • 1365-3059
OpenAlex
W2135437376
Cited by
161
References
0
FWCI
1.39
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: PCR‐based detection of Colletotrichum acutatum on strawberry. https://app.cochat.ai/papers/10.1046/j.1365-3059.1996.d01-3.x
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SREENIVASAPRASAD, S., SHARADA, K., BROWN, A. E., & MILLS, P. R. (1996). PCR‐based detection of Colletotrichum acutatum on strawberry. Plant Pathology. https://doi.org/10.1046/j.1365-3059.1996.d01-3.x

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