2001
DOI: 10.1017/s0953756200003725
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Analysis of partial Glomales SSU rRNA gene sequences: implications for primer design and phylogeny

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Cited by 127 publications
(71 citation statements)
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References 48 publications
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“…The fact that the isolated Leptosphaeria sp. contained sequences very closely matching those of T1 and T3 (9,20) makes it very likely that the previously reported sequences T1 and T3 also came from a fungus in the Leptosphaeria genus living inside healthy S. castanea spores rather than as contaminants on the surface of the spores as previously suggested (24). The further observation of fungal hyphae inside S. castanea spores with a morphology similar to that of the isolated Leptosphaeria sp.…”
supporting
confidence: 79%
See 1 more Smart Citation
“…The fact that the isolated Leptosphaeria sp. contained sequences very closely matching those of T1 and T3 (9,20) makes it very likely that the previously reported sequences T1 and T3 also came from a fungus in the Leptosphaeria genus living inside healthy S. castanea spores rather than as contaminants on the surface of the spores as previously suggested (24). The further observation of fungal hyphae inside S. castanea spores with a morphology similar to that of the isolated Leptosphaeria sp.…”
supporting
confidence: 79%
“…The question therefore arises as to what is the true origin of these sequences. Other researchers have suggested that these sequences are the result of fungal contaminants on the AMF spore wall (24). Three possibilities were suggested by Redecker et al (20): (i) that these sequences were from contaminating fungi on the surface of the AMF spores, (ii) that they were sequences from ascomycetes which were living inside S. castanea spores, and (iii) that they originated from the S. castanea genome.…”
mentioning
confidence: 99%
“…So far, to our knowledge there have been no studies combining molecular genetic variation with variation in quantitative genetic traits (QGTs) in an AMF field population. This lack of data is surprising, given that a remarkably high amount of genetic variability exists in an AMF species and within individual spores (6)(7)(8)(9)(10). AMF are coenocytic, with many nuclei coexisting in a common cytoplasm, and one species of AMF has recently been shown to be multigenomic, harboring genetically different nuclei (11).…”
mentioning
confidence: 99%
“…Nevertheless, an advantage for the use of primer pair AM1/NS31 is the relatively large amounts of DNA sequence information derived from this primer pair available. A subsequent study (Zhang et al, 2010) was aimed the variable V3-V4 region of the 18S rDNA of AMF gene, by using nested PCR in three steps: (1) first round PCR, using primers GeoA2 and Geo11 (Schwarzott and Schüssler, 2001); (2) second round, using primers above-mentioned AM1/ NS31-GC; and (3) third round using NS31-GC/Glol. In that study, the AMF community from rhizosphere of two shrubs species was investigated and the species richness ranged from 17 to 25 AMF species.…”
Section: Wwwintechopencommentioning
confidence: 99%