Pseudomonas aeruginosa adaptation to lungs of cystic fibrosis patients leads to lowered resistance to phage and protist enemies.
Pseudomonas aeruginosa adaptation to lungs of cystic fibrosis patients leads to lowered resistance to phage and protist enemies.
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DOI:
10.1371/journal.pone.0075380
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Buckling A
中科院分区:
文献类型:
--
作者:
Friman VP;Ghoul M;Molin S;Johansen HK;Buckling A
Pathogenic life styles can lead to highly specialized interactions with host species, potentially resulting in fitness trade-offs in other ecological contexts. Here we studied how adaptation of the environmentally transmitted bacterial pathogen, Pseudomonas aeruginosa, to cystic fibrosis (CF) patients affects its survival in the presence of natural phage (14/1, ΦKZ, PNM and PT7) and protist (Tetrahymena thermophila and Acanthamoebae polyphaga) enemies. We found that most of the bacteria isolated from relatively recently intermittently colonised patients (1–25 months), were innately phage-resistant and highly toxic for protists. In contrast, bacteria isolated from long time chronically infected patients (2–23 years), were less efficient in both resisting phages and killing protists. Moreover, chronic isolates showed reduced killing of wax moth larvae (Galleria mellonella) probably due to weaker in vitro growth and protease expression. These results suggest that P. aeruginosa long-term adaptation to CF-lungs could trade off with its survival in aquatic environmental reservoirs in the presence of microbial enemies, while lowered virulence could reduce pathogen opportunities to infect insect vectors; factors that are both likely to result in poorer environmental transmission. From an applied perspective, phage therapy could be useful against chronic P. aeruginosa lung infections that are often characterized by multidrug resistance: chronic isolates were least resistant to phages and their poor growth will likely slow down the emergence of beneficial resistance mutations.
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影响因子:
3.1
作者:
Johansen, HK;Norregaard, L;Hoiby, N
通讯作者:
Hoiby, N
影响因子:
4.4
作者:
Hosseinidoust, Zeinab;Tufenkji, Nathalie;van de Ven, Theo G. M.
通讯作者:
van de Ven, Theo G. M.
影响因子:
3.7
作者:
Bjarnsholt T;Jensen PØ;Jakobsen TH;Phipps R;Nielsen AK;Rybtke MT;Tolker-Nielsen T;Givskov M;Høiby N;Ciofu O;Scandinavian Cystic Fibrosis Study Consortium
通讯作者:
Scandinavian Cystic Fibrosis Study Consortium
影响因子:
6.4
作者:
Alemayehu D;Casey PG;McAuliffe O;Guinane CM;Martin JG;Shanahan F;Coffey A;Ross RP;Hill C
通讯作者:
Hill C
影响因子:
6.4
作者:
Debarbieux, Laurent;Leduc, Dominique;Touqui, Lhousseine
通讯作者:
Touqui, Lhousseine