Coincidental loss of bacterial virulence in multi-enemy microbial communities

Autor: Johanna Mappes, Anni-Maria Örmälä-Odegrip, Ji Zhang, Tarmo Ketola, Jouni Laakso
Přispěvatelé: Biosciences
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Ecological selection
Bacteriophage
Natural Selection
Bacteriophages
ANTAGONISTIC COEVOLUTION
LISTERIA-MONOCYTOGENES
Serratia marcescens
1183 Plant biology
microbiology
virology

Genetics
SERRATIA-MARCESCENS
Acanthamoeba castellanii
0303 health sciences
Multidisciplinary
Ecology
biology
Tetrahymena
Medicine
Research Article
Evolutionary Processes
Virulence Factors
Antagonistic Coevolution
Science
Microbial Consortia
education
Virulence
Microbiology
Microbial Ecology
Evolution
Molecular

03 medical and health sciences
multi-enemy microbial communities
Water environment
030304 developmental biology
STAPHYLOCOCCUS-AUREUS
Evolutionary Biology
PSEUDOMONAS-AERUGINOSA VIRULENCE
030306 microbiology
bacterial virulence
DICTYOSTELIUM-DISCOIDEUM
Biology and Life Sciences
Bacteriology
biology.organism_classification
Organismal Evolution
Artificial Selection
TETRAHYMENA-THERMOPHILA
Evolutionary Ecology
Microbial Evolution
ta1181
AMEBA ACANTHAMOEBA-CASTELLANII
LEGIONELLA-PNEUMOPHILA
Bacteria
MEDIA COMPOSITION INFLUENCES
Zdroj: PLoS ONE, Vol 9, Iss 11, p e111871 (2014)
PLoS ONE
ISSN: 1932-6203
Popis: The coincidental virulence evolution hypothesis suggests that outside-host selection, such as predation, parasitism and resource competition can indirectly affect the virulence of environmentally-growing bacterial pathogens. While there are some examples of coincidental environmental selection for virulence, it is also possible that the resource acquisition and enemy defence is selecting against it. To test these ideas we conducted an evolutionary experiment by exposing the opportunistic pathogen bacterium Serratia marcescens to the particle-feeding ciliate Tetrahymena thermophila, the surfacefeeding amoeba Acanthamoeba castellanii, and the lytic bacteriophage Semad11, in all possible combinations in a simulated pond water environment. After 8 weeks the virulence of the 384 evolved clones were quantified with fruit fly Drosophila melanogaster oral infection model, and several other life-history traits were measured. We found that in comparison to ancestor bacteria, evolutionary treatments reduced the virulence in most of the treatments, but this reduction was not clearly related to any changes in other life-history traits. This suggests that virulence traits do not evolve in close relation with these life-history traits, or that different traits might link to virulence in different selective environments, for example via resource allocation trade-offs. peerReviewed
Databáze: OpenAIRE