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132j 7 Quorum Sensing in <strong>Bacteria</strong>: Potential in <strong>Plant</strong> Health Protection<br />

regulatory proteins luxR and CAP [15]. Induction of transcription from lux ICDA-<br />

BEG operon increases the cellular levels of mRNA transcripts required for both<br />

bioluminescence and OOHL molecules. The autoinduction mechanism is not initiated<br />

until a population has achieved a particular cell density. There are three<br />

components that are necessary to sense cell density: (i) signal, a luxI homologue;<br />

(ii) a means of recognizing the signal (a luxR homologue); and (iii) accumulation of<br />

the signal. Signal accumulation results either from an increase in cell numbering<br />

space with limited flow through or theoretically, <strong>by</strong> enclosing the cell in a smaller<br />

space [16,17].<br />

7.3<br />

QS and <strong>Bacteria</strong>l Traits Underregulation<br />

Quorum sensing among Gram-negative bacteria is widely known and is now better<br />

understood; however, a number of Gram-positive bacteria do possess QS systems.<br />

The nature of the signal molecule is different from that of the Gram-negative<br />

bacteria. For example, in Staphylococcus aureus, LuxS system utilizes the autoinducer<br />

AI-2. Gram-positive systems differ from Gram-negative AHL system in two main<br />

factors. (i) First, the signal substances are usually peptides that frequently have<br />

posttranscriptional modifications (ii) second, the signal substances often do not<br />

diffuse into the cell to bind to a cytoplasmic protein, but signal through binding<br />

to a membrane-located part of a two-component system. The cytoplasmic response<br />

regulator part of the two-component system then activates the target gene <strong>by</strong> binding<br />

to DNA [18]. Little information is available regarding QS virulence and pathogenicity<br />

traits in certain Gram-positive bacteria such as S. aureus, S. epidermidis and some<br />

Streptococci and Bacilli have been shown to exhibit QS control [18,19]. Other traits<br />

in Gram-positive bacteria such as competence development (Streptococci), sporulation<br />

(B. subtilis) and antibiotic biosynthesis (Lactococcus lactis) are also controlled <strong>by</strong><br />

QS [20].<br />

A variety of QS signal molecules are produced <strong>by</strong> various bacteria. Interestingly,<br />

among Gram-negative bacteria, the most common QS signal molecules produced<br />

belong to the family of N-acyl-homoserine lactones (Table 7.1).<br />

Autoinduction was first described in the marine symbiotic bacterium V. fischeri<br />

(Photobacterium) [21], and AHLs were first identified in the Gram-negative marine<br />

bacteria, V. fischeri and V. harveyi, which play a central role in the regulation of<br />

bioluminescence [22,23]. Quorum sensing or cell-to-cell communication has now<br />

been discovered in a variety of Gram-negative and Gram-positive bacteria [3,24–26].<br />

A considerable amount of data has been generated on QS and QS-control traits in<br />

bacteria, especially in Gram-negative bacteria. Regulation of many bacterial traits<br />

such as production of secondary metabolites and extracellular enzymes, biofilm<br />

formation, virulence and pathogenicity, bacterial cross-communication and the like<br />

have been suspected to arise from QS. The common traits of pathogenic and plantassociated<br />

bacteria regulated <strong>by</strong> QS are given in Table 7.1 and recent reports on the<br />

QS signal molecules and QS-regulated bacterial traits are summarized below.

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