2019
DOI: 10.1016/j.hal.2018.12.001
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Distribution of Karlodinium veneficum in the coastal region of Xiangshan Bay in the East China Sea, as detected by a real-time quantitative PCR assay of ribosomal ITS sequence

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Cited by 21 publications
(7 citation statements)
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“…However, this method seems inadequate in areas where cells are not abundant enough to be easily detected. Molecular methods based on the analysis of environmental DNA (eDNA) are now used to detect the presence of rare species of microorganisms, especially for the conservation and monitoring of endangered species (Jerde et al ., 2011; Taberlet et al ., 2012; Thomsen and Willerslev, 2015; Barnes and Turner, 2016) but also for monitoring harmful algal species (Galluzzi et al ., 2004; Fitzpatrick et al ., 2010; Garvetto et al ., 2018; Huang et al ., 2019). Standard and quantitative real‐time PCR or quantitative (rt‐PCR or qPCR) methods, based on the analysis of species‐specific Internal Transcribed Spacer (ITS)‐5.8S and Large Sub Unit (LSU) ribosomal DNA, have been developed and applied to the monitoring of Ostreopsis species (Penna et al ., 2007; Battocchi et al ., 2010; Casabianca et al ., 2013, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…However, this method seems inadequate in areas where cells are not abundant enough to be easily detected. Molecular methods based on the analysis of environmental DNA (eDNA) are now used to detect the presence of rare species of microorganisms, especially for the conservation and monitoring of endangered species (Jerde et al ., 2011; Taberlet et al ., 2012; Thomsen and Willerslev, 2015; Barnes and Turner, 2016) but also for monitoring harmful algal species (Galluzzi et al ., 2004; Fitzpatrick et al ., 2010; Garvetto et al ., 2018; Huang et al ., 2019). Standard and quantitative real‐time PCR or quantitative (rt‐PCR or qPCR) methods, based on the analysis of species‐specific Internal Transcribed Spacer (ITS)‐5.8S and Large Sub Unit (LSU) ribosomal DNA, have been developed and applied to the monitoring of Ostreopsis species (Penna et al ., 2007; Battocchi et al ., 2010; Casabianca et al ., 2013, 2014).…”
Section: Introductionmentioning
confidence: 99%
“…The spike experiments for all three toxigenic species with an average recovery efficiency of~94% of the target cells over a range of 10 2 to 10 4 target cells per L revealed a very robust assay design and reliability of the quantitative field data calculations. Specific qPCR is thus confirmed to be a valuable tool for the detection and enumeration of low abundant species [77]. In addition to this and previous Amphidomataceae qPCR spike-recovery experiments [32], a direct comparison of qPCR quantification with other independent quantification methods over a larger data set is desirable.…”
Section: Plos Onementioning
confidence: 77%
“…In the sampling areas of this study, both toxic K. veneficum and nontoxic K. zhouanum were detected (Huang et al . ). Questions about how these two closely related species interact with each other, the ecological significance of population dynamics in the field, and whether the potentially nontoxic K. zhouanum supports the growth of the omnivorous mixotrophic K. veneficum should be considered for future studies in the laboratory and in the field.…”
Section: Discussionmentioning
confidence: 97%