2019
DOI: 10.1007/s42161-018-00228-9
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Molecular detection and identification of phytoplasmas in a novel 16SrI subgroup in sunflowers and cocklebur weeds

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Cited by 5 publications
(4 citation statements)
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“…Similarity coefficients derived from virtual RFLP analysis of 16S rRNA genes of strain PLH102-1 and other 16SrI subgroups were less than or equal to 0.97, the threshold for a new subgroup delineation [ 26 ]. Therefore, strain PLH102-1 was designated as a new subgroup 16SrI-AO ( Table 2 [ 10 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 ], some of previously reported 16SrI subgroups were reassigned due to duplication).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Similarity coefficients derived from virtual RFLP analysis of 16S rRNA genes of strain PLH102-1 and other 16SrI subgroups were less than or equal to 0.97, the threshold for a new subgroup delineation [ 26 ]. Therefore, strain PLH102-1 was designated as a new subgroup 16SrI-AO ( Table 2 [ 10 , 27 , 28 , 29 , 30 , 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 , 49 , 50 ], some of previously reported 16SrI subgroups were reassigned due to duplication).…”
Section: Resultsmentioning
confidence: 99%
“…( b ) This is a re-designation of a subgroup pattern (16SrI-AI) established by Perez-Lopez et al [ 40 ]. The reason for the re-designation is that the subgroup letter 16SrI-AI had been previously published by Zhang et al [ 47 ]. ( c ) This is re-designation of the subgroup 16SrI-AG reported by Santos-Cervantes et al [ 36 ] as the subgroup letter 16SrI-AG (MH279522) had already been assigned to NS1P1cB, BS, blueberry stunt, Canada.…”
Section: Figurementioning
confidence: 99%
“…The reason of the unspecific digestion was kept unknown. It is known that phytoplasmas of 16SrI are the main group occurred in China (Li, Zhang, Liu, et al, 2012), and various subgroups and novel subgroups were discovered (Li, Zhang, Liu, et al, 2012; Li et al., 2014; Luan et al., 2018; Tseng et al., 2016; Zhang et al., 2019). In this work, we extended the queue of 16SrI subgroups with another two novel subgroups of 16SrI‐AK and ‐AL.…”
Section: Discussionmentioning
confidence: 99%
“…With the DNA as template, attempts to amplify partial 16S rRNA gene and rp genes were performed using published primers in polymerase chain reaction (PCR). In the PCR, TaKaRa Taq (TaKaRa) was the choice of DNA polymerase, and a total volume of 25 μl was set up as described previously (Zhang et al., 2019). To generate 16S rRNA gene fragments (F2nR2 region), the primer pair P1/P7 (Deng & Hiruki, 1991; Schneider, Seemüller, Smart, & Kirkpatrick, 1995) was used in a first run of PCR, followed by a second run of PCR using primer pair R16F2n/R16R2 (Gundersen & Lee, 1996); the PCR cycling conditions were set up as described previously by Nejat, Sijam, Abdullah, Vadamalai, and Dickinson (2010) and Lee et al.…”
Section: Methodsmentioning
confidence: 99%