2009
DOI: 10.5423/ppj.2009.25.3.236
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Morphometric and Genetic Variability Among Tylenchulus semipenetrans Populations from Citrus Growing Area in Korea

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Cited by 10 publications
(12 citation statements)
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“…Choi (2001) described a population of this species with slightly shorter male stylet (7-19 vs 10-12 µm) and spicules (17-22 vs 14-18 µm). Compared with the material examined byPark et al (2009), the Iranian population differs in PVSL (vs 23.6-44.5 µm) male stylet…”
mentioning
confidence: 93%
“…Choi (2001) described a population of this species with slightly shorter male stylet (7-19 vs 10-12 µm) and spicules (17-22 vs 14-18 µm). Compared with the material examined byPark et al (2009), the Iranian population differs in PVSL (vs 23.6-44.5 µm) male stylet…”
mentioning
confidence: 93%
“…The newly obtained sequences for each gene were aligned using ClustalX 1.83 (Thompson et al, 1997) with default parameters with their corresponding published gene sequences, ITS-rRNA or D2-3 of 28S rRNA, re-spectively (Subbotin et al, 2006;Park et al, 2009;Liu et al, 2011;Chen et al, unpubl.). Outgroup taxa for each dataset were chosen according to the results of previous published data (Subbotin et al, 2005(Subbotin et al, , 2006Bert et al, 2008;Holterman et al, 2009).…”
Section: Sequence and Phylogenetic Analysismentioning
confidence: 99%
“…Heterogeneity of the ITS-rRNA region for T. floridensis was revealed by enzymes BsuRI, BseNI and Hin6I. Wang et al (2004) and Park et al (2009) were the first to present diagnostic PCR-ITS-RFLP profiles for the citrus root nematode, T. semipenetrans, from China and Korea, respectively. Park et al (2009) revealed the heterogeneity of the ITS region after digestion by MseI and MspI and the presence of two ITS haplotypes.…”
Section: Molecular Diagnostics Of Tylenchulus Speciesmentioning
confidence: 99%
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“…In particular, it is difficult to distinguish J2 of T. semipenetrans from many other plant-parasitic and non-plant-parasitic nematode species microscopically. As an alternative strategy for T. semipenetrans identification, molecular diagnostic methods based on polymerase chain reaction (PCR) have been developed and applied, including PCR-restriction fragment length polymorphism (RFLP) of the internal transcribed spacer region (ITS) (Maafi et al, 2012; Park et al, 2009) and PCR with species-specific primer sets designed from rDNA-ITS (Liu et al, 2011; Maafi et al, 2012). While PCR-based detection methods provided faster, more reliable and more sensitive tools for T. semipenetrans identification when compared with traditional morphological method, they are not generally available for routine practical applications at grassroots quarantine stations and plant protection organizations because expensive and sophisticated laboratory equipment and skilled technicians are needed.…”
mentioning
confidence: 99%