Persister Cells in E. coli: Difference between revisions

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==Types of Persistence==
==Types of Persistence==


[[Image: Suarezfig1final.gif|thumb|500px|right|Figure 2. The difference between resistance and persistence. Resistance is genetic and persistence is phenotypic. Resistance produces a population of purely resistant cells. Persistence repopulates with a population of same sensitivity as before. <sup>6</sup>]]
[[Image: Suarezfig1final.gif|thumb|400px|right|Figure 2. The difference between resistance and persistence. Resistance is genetic and persistence is phenotypic. Resistance produces a population of purely resistant cells. Persistence repopulates with a population of same sensitivity as before. <sup>6</sup>]]


Persistence is triggered by environmental and [http://en.wikipedia.org/wiki/Intracellular intracellular] stressors. While the process of differentiation is not completely understood, there is some evidence suggesting how and why cells become persistent. It should be noted that persistence is not the same as resistance (Figure 1). There are two different types of persistence.  
Persistence is triggered by environmental and [http://en.wikipedia.org/wiki/Intracellular intracellular] stressors. While the process of differentiation is not completely understood, there is some evidence suggesting how and why cells become persistent. It should be noted that persistence is not the same as resistance (Figure 1). There are two different types of persistence.  

Revision as of 02:01, 16 April 2014

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Figure 1. A gram-stain of Escherichia coli

Bacterial communities form dormant, antibiotic tolerant cells called persister cells.5 These cells are not mutants, but phenotypic variants of the wild type.5 Persisters are selected to increase chances of survival in fluctuating environments.2. The diminished (or in some cases, overproduction) activity of key molecules in the cell, as well as non-growing or reduced growth rate, make cells in dormant state distinguishable.2 Persisters are found in all phases of cell growth and are non-dividing with a reduced metabolism.2,10 The slow growth of the persister cells protects them from antibiotics.1 Cells in the persister state are highly immune to bacterial antibiotics, which interfere with processes of key molecules.1 Persisters may represent the long-looked-for explanation for biofilm tolerance to antibiotics.6 There has been extensive research performed on the persister cells in Escherichia coli (Figure 2), why they do not make persisters in early-exponential growth, which indicates presence of specific persister genes.5

Types of Persistence

Figure 2. The difference between resistance and persistence. Resistance is genetic and persistence is phenotypic. Resistance produces a population of purely resistant cells. Persistence repopulates with a population of same sensitivity as before. 6

Persistence is triggered by environmental and intracellular stressors. While the process of differentiation is not completely understood, there is some evidence suggesting how and why cells become persistent. It should be noted that persistence is not the same as resistance (Figure 1). There are two different types of persistence.

Type I persisters are triggered to differentiate and become physiologically antibiotic tolerant, using strategies to resist persistence unless exposed to stressful conditions, such as starvation. This suggests that the bacteria sense these stressful environments and in preparation, push part of the population to become dormant. The rest of the population is left to thrive and risk death.1 Type I persisters are generated at the stationary phase of bacterial growth.2

Type II persisters are repetitively produced without environmental triggers and stressors and are slow growing.1 These “bet-hedging” strategies of persistence are believed to have evolved from antibiotic stressors and stress imposed on bacteria by prophages.7

Genetic Mechanisms

There are at least 37 known types of Toxin-Antitoxin (TA) systems in Escherichia coli, which are thought to be the genetic basis for the formation of persisters from normal cells.10 These toxin mechanisms usually consist of two genes encoding for stable toxins that disturb essential processes, and an unstable antitoxin that remedies the effects of the toxin.10 Toxin genes always code for proteins and the antitoxins code for either protein or RNA.3

Under type I conditions, the antitoxins are degraded by proteases in the cell, ClpXp or Lon, and the toxins are released to do their typical function in the cell.3 The most well depicted system is the Type II TA system, made up of a two-gene operon which encodes a stable toxin and an unstable antitoxin, MqsR/MqsRA. This TA system produces proteins that come together to form a complex that is not toxic. The antitoxin mqsA can be found just below the mqsR in the same operon, and encodes a slightly longer amino acid protein that neutralizes mqsR toxicity. 3 Evidence suggests that the mqsRA TA system plays an important part in many of Escherichia coli cellular processes. Deletion of mqsR and the mqsRA operon decreased persister cell formation, while mqsR overexpression increased persister formation. This is important because mqsA has also been shown to serve as a transcriptional regulator of several Escherichia coli genes, including general response regulators, as well as the mqsRA operon.3


The first candidate persister gene identified was the hipA gene encoded by the hipBA locus. HipA is a protein kinase that makes EF-Tu nonfunctional by phosphorylation. This inhibits protein synthesis and leads to tolerance of many drugs, possibly even persister formation.5


Section 3

Further Reading

[1] Antibiotic/Antimicrobial Resistance information from the Center of Disease Control and Prevention

References

1Balaban, Nathalie Q., et al. "A problem of persistence: still more questions than answers?." Nature Reviews Microbiology 11.8 (2013): 587-591.

2Balaban, Nathalie Q., et al. "Bacterial persistence as a phenotypic switch." Science 305.5690 (2004): 1622-1625.

3Brown, Breann L., et al. "The Escherichia coli toxin MqsR destabilizes the transcriptional repression complex formed between the antitoxin MqsA and the mqsRA operon promoter." Journal of Biological Chemistry 288.2 (2013): 1286-1294.

4Cheow, Wean Sin, Matthew Wook Chang, and Kunn Hadinoto. "Antibacterial efficacy of inhalable levofloxacin-loaded polymeric nanoparticles against E. coli biofilm cells: the effect of antibiotic release profile." Pharmaceutical research 27.8 (2010): 1597-1609.

5Dörr, Tobias, Marin Vulić, and Kim Lewis. "Ciprofloxacin causes persister formation by inducing the TisB toxin in Escherichia coli." PLoS biology 8.2 (2010): e1000317.

6Fauvart, Maarten, Valerie N. De Groote, and Jan Michiels. "Role of persister cells in chronic infections: clinical relevance and perspectives on anti-persister therapies." Journal of medical microbiology 60.6 (2011): 699-709.

7 Gefen, Orit, and Nathalie Q. Balaban. "The importance of being persistent: heterogeneity of bacterial populations under antibiotic stress." FEMS microbiology reviews 33.4 (2009): 704-717

8Gefen, Orit, et al. "Single-cell protein induction dynamics reveals a period of vulnerability to antibiotics in persister bacteria." Proceedings of the National Academy of Sciences 105.16 (2008): 6145-6149.

9Hofsteenge, Niels, Erik van Nimwegen, and Olin K. Silander. "Quantitative analysis of persister fractions suggests different mechanisms of formation among environmental isolates of E. coli." BMC microbiology 13.1 (2013): 25.

10 Kwan, Brian W., et al. "Arrested protein synthesis increases persister-like cell formation." Antimicrobial agents and chemotherapy 57.3 (2013): 1468-1473.


Edited by Michelle Suarez, a student of Nora Sullivan in BIOL168L (Microbiology) in The Keck Science Department of the Claremont Colleges Spring 2014.