Conferências do cE3c

Sala 2.2.14, FCUL, Lisboa

Por Klaus Harms e João A. Gama (“The Arctic University of Norway", Tromsø, Norway).


How bacteria feed and breed on fragmented, random environmental DNA | 11h00-11h45
Klaus Harms
“The Arctic University of Norway", Tromsø, Norway

Bacteria propagate by cell division, resulting in offspring cells that are, save for mutations, genetically identical with their ancestors. However, bacteria can dramatically increase genetic diversity through so-called horizontal gene transfer (HGT). In the course of HGT, external intraspecies DNA that reaches the cytoplasm can be recombined with the cellular DNA, allowing uncoupled mixing of alleles and resulting in population structures that resemble those of sexual organisms. More rarely, HGT leads to acquisition of foreign DNA that contains novel genetic information. In an evolutionary perspective, such new DNA enables bacteria to develop novel traits and to conquer previously inaccessible environmental niches.
HGT can be conferred through transduction, conjugation, transformation and, less frequently, through a number of further, less well characterized processes. Natural transformation is the active uptake of DNA from the environment by bacteria and its subsequent integration into the genome. A prerequisite for naturally transformable bacteria is the initiation of a physiological state named competence for DNA uptake.
DNA is released into the environment mostly by dead organisms, but some bacteria also actively excrete DNA. Under many environmental conditions, free DNA is quickly degraded by fragmentation and further chemical damages such as deamination, base loss, or cross-links with organic molecules. Moreover in complex environments, heterologous DNA vastly outnumbers the available homologous DNA. On the other hand, even heavily fragmented, chemically damaged, and fragmentary heterologous DNA can still transform bacteria, but the result is not acquisition of genes, but mutational modification of the bacterial genomic DNA. In this talk, I describe the mechanisms, benefits, and constraints of natural transformation by such DNA substrates.


Why some E. coli strains are not good plasmid hosts | 11h45-12h30
João A. Gama
“The Arctic University of Norway", Tromsø, Norway

Escherichia coli comprises strains ranging from commensal to pathogenic. Some of them may harbour accessory genetic elements such as plasmids, which play an important role in bacterial adaptation. However, plasmids can be lost in the absence of selection, as shown with model organisms. We studied the effects of a clinical plasmid encoding antibiotic resistance against carbapenems (last resort antibiotics) on a sample of clinical E. coli representing different sequence types (ST).
We aim to understand how different E. coli strain backgrounds face plasmid acquisition.
Most strains maintained the plasmid for ≈300 generations. Compared to other strains, ST73 strains grew slower when acquiring the plasmid (plasmid fitness cost). Moreover, plasmid conjugative transfer from the original isolate was particularly lower into ST73 strains. In agreement, analysis of E. coli genomes revealed lower frequency of plasmids in ST73 genomes than in the other STs studied. Defense mechanisms against horizontal gene transfer, such as restriction-modification systems, could be responsible for this behaviour. Comprehensive bioinformatical analysis showed that type III restriction-modification systems are more frequently present in ST73 genomes. Furthermore, there is a negative correlation between plasmid carriage and presence of type III restriction-modification systems among ST73 genomes.
Overall, these data may explain, at least in part, why molecular epidemiology studies suggest that ST73 is less associated with antibiotic resistance determinants.

11h00-12h30
cE3c - Centro de Ecologia, Evolução e Alterações Ambientais

Seminário do Laboratório de Instrumentação e Física Experimental de Partículas, por Pedro Cruz (Northeastern University).

Logótipo do EVM 2024

Por Giosuè Muratore (DM Ciências ULisboa e CMAFcIO).

Logótipo do EVM 2024

Por Pedro Duarte (DM Ciências ULisboa, CMAFcIO).

Título do programa, sobre mosaico de fotografias de jovens cientistas

As candidaturas encontram-se encerradas. Obrigada aos quase 80 candidatos/as!

Fotografia de ilha

Seminários Doutorais no âmbito da disciplina de Projeto de Investigação (Doutoramento em Ciências do Mar).

Logótipo do EVM 2024

Por Maria Manuel Torres (DM Ciências ULisboa e CMAFcIO).

Seminário do Centro de Matemática, Aplicações Fundamentais e Investigação Operacional, por Baptiste Claustre (aluno ENS Lyon, estagiário CMAFcIO).

Logótipo do EVM 2024

Por: Jorge Buescu (DM Ciências ULisboa e CMAFcIO).

Titulo e data do evento, com imagem de ponte sobre o tejo

Um evento organizado no âmbito da Ação COST EURO-MIC, de cujo Comitê de Gestão Elisabete Silva, líder do Bioactive and Multifunctional Materials Lab do BioISI, faz parte.

Logótipo do EVM 2024

Por Jean-Baptiste Casteras (DM Ciências ULisboa e CMAFcIO).

Chegou a hora: os participantes do Programa Ser Cientista vão apresentar os projetos que desenvolveram ao longo de uma semana, acompanhados por docentes e investigadores de CIÊNCIAS. E todos podem assistir!

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Extended enrolement date until July 12th.

Logótipo do evento, sobre um fundo branco

Um evento de reunião da comunidade nacional nas diversas vertentes da informática, com a ambição de ser o fórum de eleição para a divulgação, discussão e reconhecimento de trabalhos científicos.

Are you ready for this year's edition?

Imagem do evento - título, local e data do evento

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A leading venue for presenting and discussing the latest research, industrial practice and innovations in dependable and secure computing.