2008
DOI: 10.1038/ismej.2008.13
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AHL-driven quorum-sensing circuits: their frequency and function among the Proteobacteria

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Cited by 258 publications
(209 citation statements)
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“…At the station at 28.6 o N 65.1 o W, Trichodesmium colonies were also assayed using a cell-specific APase method (Dyhrman et al, 2002), and microscopic inspection clearly showed APase activity by epibionts in the colonies (Figure 2), particularly in the colonies exposed to the AHL cocktail (although this method is qualitative and not amenable to rigorous statistical comparisons (Hynes et al, 2009)). Given this observation, and the fact that available genomes from cyanobacteria, including Trichodesmium, lack clear homologs of genes encoding known AHL receptors (Case et al, 2008), we posit that the increase in APase activity (Figure 1) primarily reflected the response of bacterial epibionts and not the response of Trichodesmium. Although Trichodesmium does contain genes that align weakly at the amino acid level to authentic LuxR homologs, the key residues in the AHL-binding regions (Vannini et al, 2002;Pantankar and González, 2009) are absent, indicating that these Trichodesmium genes are unlikely to have AHLbinding functionality (Supplementary Figure 3).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…At the station at 28.6 o N 65.1 o W, Trichodesmium colonies were also assayed using a cell-specific APase method (Dyhrman et al, 2002), and microscopic inspection clearly showed APase activity by epibionts in the colonies (Figure 2), particularly in the colonies exposed to the AHL cocktail (although this method is qualitative and not amenable to rigorous statistical comparisons (Hynes et al, 2009)). Given this observation, and the fact that available genomes from cyanobacteria, including Trichodesmium, lack clear homologs of genes encoding known AHL receptors (Case et al, 2008), we posit that the increase in APase activity (Figure 1) primarily reflected the response of bacterial epibionts and not the response of Trichodesmium. Although Trichodesmium does contain genes that align weakly at the amino acid level to authentic LuxR homologs, the key residues in the AHL-binding regions (Vannini et al, 2002;Pantankar and González, 2009) are absent, indicating that these Trichodesmium genes are unlikely to have AHLbinding functionality (Supplementary Figure 3).…”
Section: Resultsmentioning
confidence: 99%
“…However, the distribution of APase activity among epibionts and Trichodesmium within colonies is highly variable even within the same environment (Dyhrman et al, 2002;Hynes et al, 2009), and the mechanisms driving the variability in this behavior are unknown. Proteobacteria related to those within Trichodesmium consortia (Hewson et al, 2009;Hmelo, 2010) are known to employ quorum sensing (QS; a cell-density dependent signaling system), based on acylated homoserine lactones (AHLs; Supplementary Figure 1) to coordinate their behavior (Wagner-Döbler et al, 2005;Case et al, 2008). Furthermore, it was recently shown that AHL-based QS is sustainable at the cell densities typical of Trichodesmium colonies (Hmelo and Van Mooy, 2009;Hmelo et al, in press).…”
Section: Introductionmentioning
confidence: 99%
“…For example, it has been shown that Escherichia coli, which does not produce AHLs, can respond to AHLs via the orphan AHL receptor SdiA, leading to specific changes in gene expression (Hughes et al, 2010). Moreover, a phylogenetic survey by Case et al (2008) demonstrated that 45 out of 512 complete genomes contained incomplete QS circuits, with homologues of the AHL receptor gene luxR but not the AHL synthase gene luxI. In our system, it was observed that several members of two dominant genera in the community, that is, Candidatus Competibacter and Candidatus Accumulator, previously demonstrated to be essential for granulation through the production of granulan associated with the EPS (Seviour et al, 2011), were positively correlated with QS and granulation (cluster 2), suggesting that they may participate in, or benefit from, QS even though they have not yet been demonstrated to produce AHL signals or carry AHL receptor homologues.…”
Section: Discussionmentioning
confidence: 99%
“…In this particular case, a combination of different LuxR homologs code for 6 different AHLs: C8HSL, C10HSL, OHC6HSL, OHC8HSL, OHC10HSL and OHC12HSL [164]. In Burkholderia mallei, 2-5 homologs of LuxR exist and it may overcome the effect of QSI by over expressing the signal molecule for one such homolog [165]. This repertoire of different signal synthases and signals provides a safeguard.…”
Section: Duplications In Qssmentioning
confidence: 99%