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Primitive But Intelligent: Bacterial Quorum Sensing - Lecture Notes | MCB 741, Papers of Biology

Material Type: Paper; Class: SEMINAR IN MCB; Subject: Molecular and Cellular Biology (MCB); University: Ohio University; Term: Winter 2006;

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MCB 741 Yanyan Cao
Primitive but intelligent ---- Bacterial quorum sensing
Bacteria are the simplest creatures that are considered alive nowadays. Although it has long been known
that bacteria are able to secrete secondary metabolites, not until the late 1960s had we realized that such
simple organisms are able to “talk” to each other using some of the secreted metabolites. Those
molecular messengers were later named as autoinducers (1). The phenomenon of employing
autoinducers by bacteria to regulate gene expression to coordinate community behavior in response to
cell density was termed “quorum sensing” (1).
Quorum sensing was first described by Hastings’s group in 1970 when they observed that the
luminous marine bacteria Vibrio fischeri (Photobacterium fischeri) do not luminesce until they reach a
high population density (1-4). Their research further indicated that the autoinduction of bioluminescence
is regulated transcriptionally by some secreted “autoinducers” (2, 3). This particular autoinducer was
later isolated and characterized to be N-(3-oxohexanoyl)-3-aminodihydro-2(3H)-furanone or N-( -
ketocaproyl) homoserine lactone, which belongs to the N-acylhomoserine lactone (AHL) family (5).
Since then, an explosion in understanding the prevalence of quorum-sensing systems has ensued and the
pool of autoinducers has been expanding (6, 7). For instance, two other AHL family autoinducers and a
novel 4-hydroxy-2-alkylquinoline (HAQ) family autoinducer, 2-heptyl-3-hydroxy-4-quinolone (PQS)
have been identified in human facultative pathogen Pseudomonas aeruginosa (8-10). Interestingly,
recent studies recruited various antibiotics to the autoinducer group. It has been revealed that some
antibiotics at subinhibitory concentrations are not only able to activate some chromosomal gene
promoters (11-13) but also modulate some physical characteristics of communities (12). As an example,
the P. aeruginosa pigment pyocyanin, which possesses antibiotic activity, upregulates the expression of
a cluster of genes involved in virulence (13) and favors the formation of confined and smooth colonies
(12). With the rapid expanding of the knowledge about autoinducers and quorum sensing system, we are
on the way to identify a novel target for antimicrobial drug therapy (14).
References
1. González, JE & Keshavan, ND. (2006) Microbiol. Mol. Biol. Rev. 70, 859-875.
2. Nealson, KH, et. al. (1970) J. Bacteriol. 104, 313-322.
3. Nealson, KH. (1977) Arch. Microbiol. 112, 73-79.
4. Reading, NC & Sperandio, V. (2006) FEMS. Microbiol. Lett. 254, 1-11.
5. Eberhard, A, et. al. (1981) Biochemistry. 20, 2444-2449.
6. March, JC & Bentley, WE. (2004) Curr. Opin. Biotechnol. 15, 495-502.
7. Shank, EA & Kolter, R. (2009) Curr. Opin. Microbiol. 12, 1-10.
8. Pearson, JP, et. al. (1994) Proc. Natl. Acad. Sci. USA. 91, 197-201.
9. Pesci, EC, et. al. (1999) Proc. Natl. Acad. Sci. USA. 96, 11229-11234.
10. Déziel, E, et. al. (2004) Proc Natl Acad Sci U S A. 101, 1339-1344.
11. Goh, E, et.al. (2002) Proc. Natl. Acad. Sci. USA. 99(26):17025-17030.
12. Dietrich, LE, et. al. (2008) Science. 321, 1203-1206.
13. Dietrich, LE, et. al. (2006) Mol. Microbiol. 61, 1308-1321.
14. Otto, M. (2004) FEMS. Microbiol. Lett. 241, 135-141.

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MCB 741 Yanyan Cao

Primitive but intelligent ---- Bacterial quorum sensing

Bacteria are the simplest creatures that are considered alive nowadays. Although it has long been known that bacteria are able to secrete secondary metabolites, not until the late 1960s had we realized that such simple organisms are able to “talk” to each other using some of the secreted metabolites. Those molecular messengers were later named as autoinducers (1). The phenomenon of employing autoinducers by bacteria to regulate gene expression to coordinate community behavior in response to cell density was termed “quorum sensing” (1).

Quorum sensing was first described by Hastings’s group in 1970 when they observed that the luminous marine bacteria Vibrio fischeri ( Photobacterium fischeri ) do not luminesce until they reach a high population density (1-4). Their research further indicated that the autoinduction of bioluminescence is regulated transcriptionally by some secreted “autoinducers” (2, 3). This particular autoinducer was later isolated and characterized to be N -(3-oxohexanoyl)-3-aminodihydro-2(3 H )-furanone or N -( - ketocaproyl) homoserine lactone, which belongs to the N-acylhomoserine lactone (AHL) family (5). Since then, an explosion in understanding the prevalence of quorum-sensing systems has ensued and the pool of autoinducers has been expanding (6, 7). For instance, two other AHL family autoinducers and a novel 4-hydroxy-2-alkylquinoline (HAQ) family autoinducer, 2-heptyl-3-hydroxy-4-quinolone (PQS) have been identified in human facultative pathogen Pseudomonas aeruginosa (8-10). Interestingly, recent studies recruited various antibiotics to the autoinducer group. It has been revealed that some antibiotics at subinhibitory concentrations are not only able to activate some chromosomal gene promoters ( 11 - 13 ) but also modulate some physical characteristics of communities ( 12 ). As an example, the P. aeruginosa pigment pyocyanin, which possesses antibiotic activity, upregulates the expression of a cluster of genes involved in virulence (1 3 ) and favors the formation of confined and smooth colonies (1 2 ). With the rapid expanding of the knowledge about autoinducers and quorum sensing system, we are on the way to identify a novel target for antimicrobial drug therapy ( 14 ).

References

  1. González, JE & Keshavan, ND. (2006) Microbiol. Mol. Biol. Rev. 70, 859-875.
  2. Nealson, KH, et. al. (1970) J. Bacteriol. 104, 313-322.
  3. Nealson, KH. (1977) Arch. Microbiol. 112, 73-79.
  4. Reading, NC & Sperandio, V. (2006) FEMS. Microbiol. Lett. 254, 1-11.
  5. Eberhard, A, et. al. (1981) Biochemistry. 20, 2444-2449.
  6. March, JC & Bentley, WE. (2004) Curr. Opin. Biotechnol. 15, 495-502.
  7. Shank, EA & Kolter, R. (2009) Curr. Opin. Microbiol. 12, 1-10.
  8. Pearson, JP, et. al. (1994) Proc. Natl. Acad. Sci. USA. 91, 197-201.
  9. Pesci, EC, et. al. (1999) Proc. Natl. Acad. Sci. USA. 96, 11229-11234.
  10. Déziel, E, et. al. (2004) Proc Natl Acad Sci U S A. 101, 1339-1344.
  11. Goh, E, et.al. ( 2002 ) Proc. Natl. Acad. Sci. USA. 99(26):17025- 17030.
  12. Dietrich, LE, et. al. ( 2008 ) Science. 321 , 1203 - 1206.
  13. Dietrich, LE, et. al. ( 2006 ) Mol. Microbiol. 61 , 1308 - 1321.
  14. Otto, M. (2004) FEMS. Microbiol. Lett. 241, 135-141.