2001
DOI: 10.1007/bf02772897
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Angiosperm DNA contamination by endophytic fungi: Detection and methods of avoidance

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Cited by 28 publications
(13 citation statements)
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“…Storage of some of the specimens for many years in herbaria did not compromise DNA extraction or the quality of AFLP profiles. We have also demonstrated the utility in this organism of using ITS-2 PCR to screen for fungal contamination, a method reviewed and advocated by Saar et al (32) for angiosperm DNA. Our use of this PCR screen resulted in the exclusion of five contaminated individuals but also provided the useful information that G. laevigata does not harbor obligate endophytic fungi of appreciable quantity to interfere with future molecular studies.…”
Section: Discussionmentioning
confidence: 80%
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“…Storage of some of the specimens for many years in herbaria did not compromise DNA extraction or the quality of AFLP profiles. We have also demonstrated the utility in this organism of using ITS-2 PCR to screen for fungal contamination, a method reviewed and advocated by Saar et al (32) for angiosperm DNA. Our use of this PCR screen resulted in the exclusion of five contaminated individuals but also provided the useful information that G. laevigata does not harbor obligate endophytic fungi of appreciable quantity to interfere with future molecular studies.…”
Section: Discussionmentioning
confidence: 80%
“…The ITS-2 region was amplified with the primers ITS4 and ITS3 (32). We labeled the ITS3 primer with the blue fluorophore 6-FAM on the 5Ј end.…”
Section: Distribution Of Samplesmentioning
confidence: 99%
“…Therefore, it should not be surprising then that E+ plant tissues have been found to exhibit different chemical profiles from E-plant tissues (Petrini et al 1992, Saikkonen et al 1998, Yue et al 2000, 2001; L. C. Mejia, T. Gianfagna, and E. A. Herre, unpublished manuscript). Even genetic content that has been attributed to being of plant origin sometimes turns out to be derived from the fungi (Camacho et al 1997, Chiang et al 2001, Saar et al 2001.…”
Section: Discussionmentioning
confidence: 99%
“…Instead, we designed a single species-specific primer that could be paired with the universal ITS5m primer (Saar et al 2001) in all PCR reactions. By doing this, we reduced the amount of unique sequence necessary for positive species identification to about 20 bp.…”
Section: Species Specific Primer Designmentioning
confidence: 99%