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1.
Proc Biol Sci ; 289(1974): 20212486, 2022 05 11.
Artigo em Inglês | MEDLINE | ID: mdl-35506221

RESUMO

For antibiotic resistance to arise, new resistant mutants must establish in a bacterial population before they can spread via natural selection. Comprehending the stochastic factors that influence mutant establishment is crucial for a quantitative understanding of antibiotic resistance emergence. Here, we quantify the single-cell establishment probability of four Escherichia coli strains expressing ß-lactamase alleles with different activity against the antibiotic cefotaxime, as a function of antibiotic concentration in both unstructured (liquid) and structured (agar) environments. We show that concentrations well below the minimum inhibitory concentration (MIC) can substantially hamper establishment, particularly for highly resistant mutants. While the pattern of establishment suppression is comparable in both tested environments, we find greater variability in establishment probability on agar. Using a simple branching model, we investigate possible sources of this stochasticity, including environment-dependent lineage variability, but cannot reject other possible causes. Lastly, we use the single-cell establishment probability to predict each strain's MIC in the absence of social interactions. We observe substantially higher measured than predicted MIC values, particularly for highly resistant strains, which indicates cooperative effects among resistant cells at large cell numbers, such as in standard MIC assays.


Assuntos
Escherichia coli , beta-Lactamas , Ágar/farmacologia , Antibacterianos/farmacologia , Escherichia coli/genética , Testes de Sensibilidade Microbiana , beta-Lactamas/farmacologia
2.
PLoS Biol ; 13(6): e1002169, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26042786

RESUMO

Reciprocal coevolution between host and pathogen is widely seen as a major driver of evolution and biological innovation. Yet, to date, the underlying genetic mechanisms and associated trait functions that are unique to rapid coevolutionary change are generally unknown. We here combined experimental evolution of the bacterial biocontrol agent Bacillus thuringiensis and its nematode host Caenorhabditis elegans with large-scale phenotyping, whole genome analysis, and functional genetics to demonstrate the selective benefit of pathogen virulence and the underlying toxin genes during the adaptation process. We show that: (i) high virulence was specifically favoured during pathogen-host coevolution rather than pathogen one-sided adaptation to a nonchanging host or to an environment without host; (ii) the pathogen genotype BT-679 with known nematocidal toxin genes and high virulence specifically swept to fixation in all of the independent replicate populations under coevolution but only some under one-sided adaptation; (iii) high virulence in the BT-679-dominated populations correlated with elevated copy numbers of the plasmid containing the nematocidal toxin genes; (iv) loss of virulence in a toxin-plasmid lacking BT-679 isolate was reconstituted by genetic reintroduction or external addition of the toxins. We conclude that sustained coevolution is distinct from unidirectional selection in shaping the pathogen's genome and life history characteristics. To our knowledge, this study is the first to characterize the pathogen genes involved in coevolutionary adaptation in an animal host-pathogen interaction system.


Assuntos
Bacillus thuringiensis/genética , Proteínas de Bactérias/genética , Evolução Biológica , Interações Hospedeiro-Patógeno/genética , Receptores de Superfície Celular/genética , Seleção Genética , Animais , Bacillus thuringiensis/patogenicidade , Caenorhabditis elegans/microbiologia , Genoma Bacteriano , Genômica , Genótipo , Proteínas de Insetos , Fenótipo , Virulência
3.
J Invertebr Pathol ; 133: 34-40, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26592941

RESUMO

In bacterial pathogens, virulence factors are often carried on plasmids and other mobile genetic elements, and as such, plasmid evolution is central in understanding pathogenicity. Bacillus thuringiensis is an invertebrate pathogen that uses plasmid-encoded crystal (Cry) toxins to establish infections inside the host. Our study aimed to quantify stability of two Cry toxin-encoding plasmids, BTI_23p and BTI_16p, under standard laboratory culturing conditions. These two plasmids are part of the genome of the B. thuringiensis strain MYBT18679, which is of particular interest because of its high pathogenicity towards nematodes. One of the plasmids, BTI_23p, was found to be highly unstable, with substantial loss occurring within a single growth cycle. Nevertheless, longer term experimental evolution in the absence of a host revealed maintenance of the plasmid at low levels in the bacterial populations. BTI_23p encodes two nematicidal Cry toxins, Cry21Aa2 and Cry14Aa1. Consistent with previous findings, loss of the plasmid abolished pathogenicity towards the nematode Caenorhabditis elegans, which could be rescued by addition of Cry21Aa2-expressing Escherichia coli. These results implicate BTI_23p as a plasmid that is required for successful infection, yet unstable when present at high frequency in the population, consistent with the role of Cry toxins as public goods.


Assuntos
Bacillus thuringiensis/patogenicidade , Proteínas de Bactérias/genética , Caenorhabditis elegans/microbiologia , Endotoxinas/genética , Proteínas Hemolisinas/genética , Plasmídeos/genética , Animais , Antinematódeos/química , Antinematódeos/farmacologia , Bacillus thuringiensis/genética , Bacillus thuringiensis/fisiologia , Toxinas de Bacillus thuringiensis , Caenorhabditis elegans/efeitos dos fármacos , Escherichia coli/genética , Interações Hospedeiro-Patógeno , Plasmídeos/fisiologia , Virulência/genética
4.
Front Microbiol ; 12: 698970, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34489889

RESUMO

For a better understanding of the evolution of antibiotic resistance, it is imperative to study the factors that determine the initial establishment of mutant resistance alleles. In addition to the antibiotic concentration, the establishment of resistance alleles may be affected by interactions with the surrounding susceptible cells from which they derive, for instance via the release of nutrients or removal of the antibiotic. Here, we investigate the effects of social interactions with surrounding susceptible cells on the establishment of Escherichia coli mutants with increasing ß-lactamase activity (i.e., the capacity to hydrolyze ß-lactam antibiotics) from single cells under the exposure of the antibiotic cefotaxime (CTX) on agar plates. We find that relatively susceptible cells, expressing a ß-lactamase with very low antibiotic-hydrolyzing activity, increase the probability of mutant cells to survive and outgrow into colonies due to the active breakdown of the antibiotic. However, the rate of breakdown by the susceptible strain is much higher than expected based on its low enzymatic activity. A detailed theoretical model suggests that this observation may be explained by cell filamentation causing delayed lysis. While susceptible cells may hamper the spread of higher-resistant ß-lactamase mutants at relatively high frequencies, our findings show that they promote their initial establishment.

5.
Aquat Toxicol ; 182: 31-38, 2017 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-27846396

RESUMO

Increases in dissolved organic carbon (DOC) in the form of humic substances, causing browning of surface water, have been reported worldwide. Field surveys indicate that higher DOC levels can influence primary production and thus plankton composition. Experimental studies on the direct effects of humic DOC on aquatic organisms have shown varying results depending on concentration and additional environmental factors. Moreover, changes in life-histories and stress responses have usually been tested separately, rather than in combination. We experimentally tested the impact of a sudden increase in humic DOC on two species of the zooplankton cladoceran Daphnia, across several levels of biological organisation, from cellular to population responses. In D. magna, strong impacts on reproduction (delayed maturity and reduced number of offspring) were coupled with overall stress induction (increases in antioxidant capacity and oxidative damage, combined with a reduced amount of available energy). In D. longispina, increased mortality and lowered fecundity were observed. We conclude that a strong input of humic DOC into aquatic systems can have severe negative impacts on zooplankton species, and has the potential to alter zooplankton community structures.


Assuntos
Carbono/toxicidade , Daphnia/efeitos dos fármacos , Substâncias Húmicas/toxicidade , Estresse Oxidativo/efeitos dos fármacos , Animais , Carbono/química , Fertilidade/efeitos dos fármacos , Água Doce/química , Poluentes Químicos da Água/toxicidade , Zooplâncton/efeitos dos fármacos
6.
Sci Rep ; 6: 35039, 2016 10 13.
Artigo em Inglês | MEDLINE | ID: mdl-27733762

RESUMO

Parasites are rarely included in food web studies, although they can strongly alter trophic interactions. In aquatic ecosystems, poorly grazed cyanobacteria often dominate phytoplankton communities, leading to the decoupling of primary and secondary production. Here, we addressed the interface between predator-prey and host-parasite interactions by conducting a life-table experiment, in which four Daphnia galeata genotypes were maintained on quantitatively comparable diets consisting of healthy cyanobacteria or cyanobacteria infected by a fungal (chytrid) parasite. In four out of five fitness parameters, at least one Daphnia genotype performed better on parasitised cyanobacteria than in the absence of infection. Further treatments consisting of purified chytrid zoospores and heterotrophic bacteria suspensions established the causes of improved fitness. First, Daphnia feed on chytrid zoospores which trophically upgrade cyanobacterial carbon. Second, an increase in heterotrophic bacterial biomass, promoted by cyanobacterial decay, provides an additional food source for Daphnia. In addition, chytrid infection induces fragmentation of cyanobacterial filaments, which could render cyanobacteria more edible. Our results demonstrate that chytrid parasitism can sustain zooplankton under cyanobacterial bloom conditions, and exemplify the potential of parasites to alter interactions between trophic levels.


Assuntos
Daphnia/fisiologia , Zooplâncton/microbiologia , Animais , Comportamento Animal , Cianobactérias/fisiologia , Daphnia/genética , Comportamento Alimentar , Cadeia Alimentar , Fungos/fisiologia , Genótipo , Interações Hospedeiro-Parasita
7.
Ecol Evol ; 5(16): 3250-63, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26380661

RESUMO

The nematode Caenorhabditis elegans is a central laboratory model system in almost all biological disciplines, yet its natural life history and population biology are largely unexplored. Such information is essential for in-depth understanding of the nematode's biology because its natural ecology provides the context, in which its traits and the underlying molecular mechanisms evolved. We characterized natural phenotypic and genetic variation among North German C. elegans isolates. We used the unique opportunity to compare samples collected 10 years apart from the same compost heap and additionally included recent samples for this and a second site, collected across a 1.5-year period. Our analysis revealed significant population genetic differentiation between locations, across the 10-year time period, but for only one location a trend across the shorter time frame. Significant variation was similarly found for phenotypic traits of likely importance in nature, such as choice behavior and population growth in the presence of pathogens or naturally associated bacteria. Phenotypic variation was significantly influenced by C. elegans genotype, time of isolation, and sampling site. The here studied C. elegans isolates may provide a valuable, genetically variable resource for future dissection of naturally relevant gene functions.

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