Page 2 Plant-Bacteria Interactions Edited by Iqbal Ahmad, John ...
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138j 7 Quorum Sensing in <strong>Bacteria</strong>: Potential in <strong>Plant</strong> Health Protection<br />
to various commercial crops such as onion, potato, carrot, celery, cucumber and pine<br />
apple. Some other species are also known to be pathogenic/opportunistic pathogens<br />
to insects and animals [103].<br />
The soft rot Erwinia spp. includes E. chrysanthemi, E. carotovora sub sp. carotovora<br />
(Ecc), E. atroseptica (Eca) and E. betavascolorum (Ecb). These organisms characteristically<br />
produced an abundance of exoenzymes including pectin methyl esterase, pectate<br />
lyase, pectin lyase, polygalacturonase, cellulose and proteases [107,108]. These enzymes<br />
are virulence factors of the bacterium. Disruption of genes encoding above<br />
enzymes often leads to reduction of virulence in planta [109,110]. Other secondary<br />
metabolites widely studied in Erwinia sp. are the production and QS-based regulation<br />
of carbapenem, a b-lactam antibiotic. The cell density-dependent production of exoenzymesinEccisalsodependentonthesynthesisofOHHL<strong>by</strong>Car1,whichencodesaluxI<br />
homologue in Ecc. Disruption of carI leads to a diminution of exoenzyme synthesis<br />
and a consequent reduction of virulence in planta [69,111]. It has been reported that<br />
CarR protein has the ability to sequester OHHL away from an additional LuxR homologue<br />
responsible for induction of exoenzymes synthesis. A second LuxR homologue<br />
expR (eccR/rexR) has been identifiedin ECC. Anderson et al. [112] deduced that control<br />
of exoenzyme production takes place through the input of many regulators, some of<br />
which interact with components of the QS system.<br />
Other species of Erwinia have been found to produce acyl-HSLs; Eca, Ebc and E.<br />
chrysanthemum synthesize different acyl-HSLs (OHHL, HHL and N-decanoyl-Lhomoserine<br />
lactone, DHL) [32,35,41].<br />
7.4.2<br />
R. solanacearum<br />
R. solanacearum causes vascular wilt disease of many plants primarily due its ability<br />
to produce an acidic exopolysaccharide and plant cell wall degrading extracellular<br />
enzymes [113]. Expression of these virulence factors occurs in an apparent cell<br />
density dependent manner, with maximum expression at high cell densities<br />
[114]. The lysR type regulator, PhcA, is central to the complex regulation of EPS<br />
and extracellular enzymes, and hence, pathogenicity in R. solanacearum. PhcA activity<br />
is regulated <strong>by</strong> a two-component regulatory system, which, in turn, is responsive<br />
to the QS signal molecules, 3-hydroxy palmitic acid methyl ester (3OHPAME).<br />
Exogenous addition of 3OHPAME to cultures at low cell density does induce precocious<br />
production of EPS and enzymes [114–116] PhcS and PhcR that makeup the<br />
two-component system responsive to 3OHPAME. It has been shown that PhcS and<br />
PhcR act together to negatively regulate the expression of PhcA-regulated genes in<br />
the absence of 3OHPAME [117].<br />
7.4.3<br />
Xanthomonas campestris<br />
Cell-to-cell communication in X. campestris (Xcc), the causative agent of the black rot<br />
of cruciferous plants, has been described. This organism also produces a variety of