Literature DB >> 21789608

The influence of P. fluorescens cell morphology on the lytic performance and production of phage φIBB-PF7A.

Sanna Sillankorva1, Diana Pires, Hugo Oliveira, Peter Neubauer, Joana Azeredo.   

Abstract

This study aims at assessing the influence of Pseudomonas fluorescence cell morphology on the effectiveness and production of the lytic bacteriophage φIBB-PF7A. P. fluorescens were cultured as rods or as elongated cells by varying the temperature and rotary agitation conditions. Cells presented rod shape when grown at temperatures up to 25°C and also at 30°C under static conditions, and elongated morphology only at 30°C when cultures were grown under agitation. Elongated cells were 0.4 up to 27.9 μm longer than rod cells. Rod-shaped hosts were best infected by phages at 25°C which resulted in an 82% cell density reduction. Phage infection of elongated cells was successful, and the cell density reductions achieved was statistically similar (P > 0.05) to those obtained at the optimum growth temperature of P. fluorescens. Phage burst size varied with the cell growth conditions and was approximately 58 and 153 PFU per infected rod and elongated cells, grown at 160 rpm, at 25°C (the optimal temperature) and 30°C, respectively. Phage adsorption was faster to elongated cells, most likely due to the longer length of the host. The surface composition of rod and elongated cells is similar in terms of outer membrane proteins and lipopolysaccharide profiles. The results of this study suggest that the change of rod cells to an elongated morphology does not prevent cells from being attacked by phages and also does not impair the phage infection.

Entities:  

Mesh:

Year:  2011        PMID: 21789608     DOI: 10.1007/s00284-011-9987-0

Source DB:  PubMed          Journal:  Curr Microbiol        ISSN: 0343-8651            Impact factor:   2.188


  25 in total

Review 1.  Themes and variations in prokaryotic cell division.

Authors:  W Margolin
Journal:  FEMS Microbiol Rev       Date:  2000-10       Impact factor: 16.408

2.  The resolution of bacteroides lipopolysaccharides by polyacrylamide gel electrophoresis.

Authors:  J P Maskell
Journal:  J Med Microbiol       Date:  1991-05       Impact factor: 2.472

3.  Identification of cell wall proteins of Bacteroides fragilis to which bacteriophage B40-8 binds specifically.

Authors:  Anna Puig; Rosa Araujo; Joan Jofre; Jorge Frias-Lopez
Journal:  Microbiology (Reading)       Date:  2001-02       Impact factor: 2.777

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Bacteriophage T4 development depends on the physiology of its host Escherichia coli.

Authors:  Hilla Hadas; Monica Einav; Itzhak Fishov; Arieh Zaritsky
Journal:  Microbiology (Reading)       Date:  1997-01       Impact factor: 2.777

6.  Bacteriophage infection is targeted to cellular poles.

Authors:  Rotem Edgar; Assaf Rokney; Morgan Feeney; Szabolcs Semsey; Martin Kessel; Marcia B Goldberg; Sankar Adhya; Amos B Oppenheim
Journal:  Mol Microbiol       Date:  2008-03-19       Impact factor: 3.501

7.  Pseudomonas fluorescens biofilms subjected to phage phiIBB-PF7A.

Authors:  Sanna Sillankorva; Peter Neubauer; Joana Azeredo
Journal:  BMC Biotechnol       Date:  2008-10-27       Impact factor: 2.563

8.  Phage-Antibiotic Synergy (PAS): beta-lactam and quinolone antibiotics stimulate virulent phage growth.

Authors:  André M Comeau; Françoise Tétart; Sabrina N Trojet; Marie-Françoise Prère; H M Krisch
Journal:  PLoS One       Date:  2007-08-29       Impact factor: 3.240

9.  The effect of chemical and physical agents on the phage receptor of Phase II Shigella sonnei.

Authors:  G T BARRY; W F GOEBEL
Journal:  J Exp Med       Date:  1951-11       Impact factor: 14.307

10.  Isolation and characterization of a T7-like lytic phage for Pseudomonas fluorescens.

Authors:  Sanna Sillankorva; Peter Neubauer; Joana Azeredo
Journal:  BMC Biotechnol       Date:  2008-10-27       Impact factor: 2.563

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.