scholarly journals GENETIC AND MORPHOTYPIC HETEROGENEITY OF SWIMMING POOL BACTERIAL POPULATIONS

2011 ◽  
Vol 9 (2) ◽  
pp. 24-33 ◽  
Author(s):  
Larisa A Magdanova ◽  
Nadezhda V Golyasnaya
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Mutation Frequency ◽  
Bacterial Species ◽  
Spontaneous Mutation ◽  
Swimming Pool ◽  
Bacillus Sp ◽  
Bacterial Populations ◽  
Pseudomonas Alcaligenes ◽  
High Level ◽  
Spontaneous Mutation Frequency

The populations of resident bacterial species of the swimming pool community such as Pseudomonas aeruginosa, Bacillus sp., Acinetobacter lwoffii and Pseudomonas alcaligenes were analyzed. All these species showed stable in time heterogeneity by spontaneous mutation frequency and biofilm forming ability. There was notably high occurrence of mutators in all investigated populations. Our results show high level of genetic plasticity and adaptivity under conditions of starvation and exposure to biocides. 

scholarly journals SPONTANEOUS UNSTABLE UNC-22 IV MUTATIONS IN C. ELEGANS VAR. BERGERAC

Genetics ◽  
1984 ◽  
Vol 108 (4) ◽  
pp. 859-877
Author(s):  
D G Moerman ◽  
R H Waterston
Keyword(s):  
Mutation Frequency ◽  
Spontaneous Mutation ◽  
Phenotypic Effect ◽  
C Elegans ◽  
High Mutation Frequency ◽  
Mutator Activity ◽  
Discrete Site ◽  
Unstable Mutations ◽  
Spontaneous Mutation Frequency ◽  
Forward Mutation

ABSTRACT This paper describes a mutator system in the nematode Caenorhabditis elegans var. Bergerac for the gene unc-22. Of nine C. elegans and two C. briggsae strains tested only the Bergerac BO strain yielded mutant animals at a high frequency and the unc-22 IV gene is a preferred mutational target. The forward spontaneous mutation frequency at the unc-22 locus in Bergerac BO is about 1 × 10-4, and most of these spontaneous unc-22 mutations revert at frequencies between 2 × 10-3 and 2 × 10-4. Both the forward mutation frequency and the reversion frequency are sensitive to genetic background. Spontaneous unc-22 mutations derived in a Bergerac background and placed in a primarily Bristol background revert at frequencies of <10-6. When reintroduced into a Bergerac/Bristol hybrid background the mutations once again become unstable. The mutator activity could not be localized to a discrete site in the Bergerac genome. Nor did mutator activity require the Bergerac unc-22 gene as a target since the Bristol unc-22 homolog placed in a Bergerac background also showed high mutation frequency. Intragenic mapping of two spontaneous unc-22 alleles, st136 and st137, place both mutations in the central region of the known unc-22 map. However, these mutations probably recombine with one another, suggesting that the unstable mutations can occur in more than one site in unc-22. Examination of the phenotypic effect of these mutations on muscle structure indicates that they are less severe in their effect than a known amber allele. We suggest that this mutator system is polygenic and dispersed over the nematode genome and could represent activity of the transposable element Tc1.

scholarly journals Spatiotemporal Distribution of Pseudomonas aeruginosa Alkyl Quinolones under Metabolic and Competitive Stress

mSphere ◽  
2020 ◽  
Vol 5 (4) ◽  
Author(s):  
Tianyuan Cao ◽  
Jonathan V. Sweedler ◽  
Paul W. Bohn ◽  
Joshua D. Shrout
Keyword(s):  
Pseudomonas Aeruginosa ◽  
Bacterial Species ◽  
Metabolic Stress ◽  
Opportunistic Pathogen ◽  
Cell Interaction ◽  
Chemical Imaging ◽  
Carbon Limitation ◽  
Bacterial Strains ◽  
Content Type ◽  
High Level

ABSTRACT Pseudomonas aeruginosa is an opportunistic human pathogen important to diseases such as cystic fibrosis. P. aeruginosa has multiple quorum-sensing (QS) systems, one of which utilizes the signaling molecule 2-heptyl-3-hydroxy-4-quinolone (Pseudomonas quinolone signal [PQS]). Here, we use hyperspectral Raman imaging to elucidate the spatiotemporal PQS distributions that determine how P. aeruginosa regulates surface colonization and its response to both metabolic stress and competition from other bacterial strains. These chemical imaging experiments illustrate the strong link between environmental challenges, such as metabolic stress caused by nutritional limitations or the presence of another bacterial species, and PQS signaling. Metabolic stress elicits a complex response in which limited nutrients induce the bacteria to produce PQS earlier, but the bacteria may also pause PQS production entirely if the nutrient concentration is too low. Separately, coculturing P. aeruginosa in the proximity of another bacterial species, or its culture supernatant, results in earlier production of PQS. However, these differences in PQS appearance are not observed for all alkyl quinolones (AQs) measured; the spatiotemporal response of 2-heptyl-4-hydroxyquinoline N-oxide (HQNO) is highly uniform for most conditions. These insights on the spatiotemporal distributions of quinolones provide additional perspective on the behavior of P. aeruginosa in response to different environmental cues. IMPORTANCE Alkyl quinolones (AQs), including Pseudomonas quinolone signal (PQS), made by the opportunistic pathogen Pseudomonas aeruginosa have been associated with both population density and stress. The regulation of AQ production is known to be complex, and the stimuli that modulate AQ responses are not fully clear. Here, we have used hyperspectral Raman chemical imaging to examine the temporal and spatial profiles of AQs exhibited by P. aeruginosa under several potentially stressful conditions. We found that metabolic stress, effected by carbon limitation, or competition stress, effected by proximity to other species, resulted in accelerated PQS production. This competition effect did not require cell-to-cell interaction, as evidenced by the fact that the addition of supernatants from either Escherichia coli or Staphylococcus aureus led to early appearance of PQS. Lastly, the fact that these modulations were observed for PQS but not for all AQs suggests a high level of complexity in AQ regulation that remains to be discerned.

Disruption of Xpg increases spontaneous mutation frequency, particularly A:T to C:G transversion

2001 ◽  
Vol 487 (3-4) ◽  
pp. 127-135 ◽  
Author(s):  
Naoko Shiomi ◽  
Emiko Hayashi ◽  
Shun-ichi Sasanuma ◽  
Kazuei Mita ◽  
Tadahiro Shiomi
Keyword(s):  
Mutation Frequency ◽  
Spontaneous Mutation ◽  
Spontaneous Mutation Frequency

Tissue-specific time courses of spontaneous mutation frequency and deviations in mutation pattern are observed in middle to late adulthood in Big Blue mice

2005 ◽  
Vol 45 (5) ◽  
pp. 442-454 ◽  
Author(s):  
Kathleen A. Hill ◽  
Asanga Halangoda ◽  
Petra W. Heinmoeller ◽  
Kelly Gonzalez ◽  
Chaniga Chitaphan ◽  
...  
Keyword(s):  
Mutation Frequency ◽  
Spontaneous Mutation ◽  
Specific Time ◽  
Late Adulthood ◽  
Tissue Specific ◽  
Mutation Pattern ◽  
Time Courses ◽  
Spontaneous Mutation Frequency

scholarly journals The mutagenicity of amino acid analogues inCoprinus lagopus

1974 ◽  
Vol 23 (1) ◽  
pp. 47-61 ◽  
Author(s):  
Philippa J. Talmud ◽  
D. Lewis
Keyword(s):  
Amino Acid ◽  
Mutation Frequency ◽  
Spontaneous Mutation ◽  
Base Change ◽  
Response Curves ◽  
Amino Acid Analogues ◽  
Single Base Change ◽  
Protein Incorporation ◽  
Dose Dependent ◽  
Spontaneous Mutation Frequency

SummaryThe amino acid analoguesp-fluorophenylalanine (PFP) and ethionine (ETH) are strongly mutagenic inCoprinus lagopus. The most pronounced effect was found with suppressor mutations of themet-1locus. PFP, at a concentration of 2·4 × 10−4M, increased the mutation frequency 500 fold and ETH, at a concentration of 2·4 × 10−3M, 30 fold over the spontaneous mutation frequency. From the spectrum of suppressors of themet-1locus and the dominant revertants of thead-82locus, induced by analogue treatments, it was concluded that both analogues induce single base-change mutations. The dose response curves follow a sigmoid plot, revealing that within a certain range of analogue concentrations, muta-genesis is strongly dose dependent.Using analogue resistant mutants, it has been shown that PFP mutagenesis is a function of its incorporation into protein. However, ETH mutagenesis is independent of protein incorporation but can be correlated with the degree of ethylation of nucleic acids. The synergistic effect PFP and ETH supports the evidence of the different mutagenic actions of the two analogues.

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