2009
DOI: 10.1007/s00227-009-1263-5
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Development of clade-specific Symbiodinium primers for quantitative PCR (qPCR) and their application to detecting clade D symbionts in Caribbean corals

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Cited by 75 publications
(78 citation statements)
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“…The samples were additionally analyzed using previously developed Clade B, C, and D specific realtime PCR primers designed to target differences in the rDNA (Correa et al 2009). This assay provides a greater level of sensitivity than PCR-DGGE for detecting the presence/absence of any low-level, background populations of Symbiodinium ).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The samples were additionally analyzed using previously developed Clade B, C, and D specific realtime PCR primers designed to target differences in the rDNA (Correa et al 2009). This assay provides a greater level of sensitivity than PCR-DGGE for detecting the presence/absence of any low-level, background populations of Symbiodinium ).…”
Section: Methodsmentioning
confidence: 99%
“…real-time PCR) have detected low-level, background symbiont populations that belong to a clade group different from the typical dominant symbiont (Loram et al 2007, Correa et al 2009, Silverstein et al 2012. These findings were used to infer that the potential of symbiont shuffling is higher than previously thought.…”
Section: Introductionmentioning
confidence: 95%
“…In late September, B1 Aiptasia was no longer detected in colonies where this symbiont occurred in abundance during the early recovery phase (figure 2b and electronic supplementary material, figure S1a). Quantitative PCR analyses of multiple independent samples from individual colonies (Correa et al 2009) were unable to detect these symbionts at background levels (data not shown).…”
Section: (F) Statistical Analysesmentioning
confidence: 98%
“…Previous studies employing variable molecular markers have shown that giant clams can harbor a mixture of Symbiodinium types (Rowan & Powers 1991, Baillie et al 2000a, as well as the present study). The bulk of recent research on Symbiodinium diversity is based on DGGE analysis of ITS2 rDNA, which has been suggested to be the most broadly applicable and appropriate marker for characterizing Symbiodinium diversity (LaJeunesse 2001, Correa et al 2009). Future applications of more sensitive molecular methods that are designed to identify Symbiodinium in low abundance (such as quantitative PCR) may re veal additional symbiont diversity within individual clams (Mieog et al 2007, Correa et al 2009).…”
Section: Mixed Symbiodinium Communities In Clam Hostsmentioning
confidence: 99%
“…First, rare types present at low abundance (up to 10 to 20% of the total symbiont population, depending on type) may not be detected by DGGE . Recent development of quantitative PCR primers for Symbiodinium enable sensitive detection of symbionts present in very low numbers, more so than is possible using PCR-DGGE (Mieog et al 2007, Correa et al 2009). Application of these techniques to giant clam-algal symbioses will increase our understanding of the utility of diverse symbionts in this system.…”
Section: Mixed Symbiodinium Communities In Clam Hostsmentioning
confidence: 99%