Generalized transduction is pivotal in bacterial evolution but lacks comprehensive understanding regarding the facilitating features and variations among phages. We addressed this gap by sequencing and comparing the transducing particle content of three different Salmonella Typhimurium phages (i.e. Det7, ES18 and P22) that share a headful packaging mechanism that is typically initiated from a cognate pac site within the phage chromosome. This revealed substantial disparities in both the extent and content of transducing particles among these phages. While Det7 outperformed ES18 in terms of relative number of transducing particles, both phages contrasted with P22 in terms of content. In fact, we found evidence for the presence of conserved P22 pac-like sequences in the host chromosome that direct tremendously increased packaging and transduction frequencies of downstream regions by P22. More specifically, a ca. 561 kb host region between oppositely oriented pac-like sequences in the purF and minE loci was identified as highly packaged and transduced during both P22 prophage induction and lytic infection. Our findings underscore the evolution of phage transducing capacity towards attenuation, promiscuity or directionality, and suggest that pac-like sequences in the host chromosome could become selected as sites directing high frequency of transduction.
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http://dx.doi.org/10.1093/nar/gkae489 | DOI Listing |
Nucleic Acids Res
July 2024
Department of Microbial and Molecular Systems, KU Leuven, Leuven, Vlaams-Brabant 3000, Belgium.
Plant Cell Physiol
March 1999
Department of Cell Biology, National Institute for Basic Biology, Okazaki, Japan.
We have previously reported that precursor-accumulating (PAC) vesicles found exclusively in developing seeds are involved in a transport of seed storage proteins, such as 2S albumin, from the endoplasmic reticulum to protein-storage vacuoles. Here, we constructed chimeric genes that encode fusion proteins consisting of both various lengths of polypeptides derived from pumpkin 2S albumin and a selectable marker enzyme, phosphinothricin acetyltransferase. The chimeric genes were expressed in transgenic Arabidopsis in order to investigate the mechanism of the PAC vesicle formation.
View Article and Find Full Text PDFJ Mol Biol
April 1995
Department of Biological Chemistry, University of Maryland School of Medicine, Baltimore 21201, USA.
Bacteriophage T4 genes 16 and 19 containing the 24 bp homology regions that recombine to form Hp17 mutants were cloned into plasmids. When the two homology sequences were cloned either together into one or separately into two compatible plasmids, a polymerase chain reaction assay showed that recombination occurred in vivo. The recombinant sequence was identical with that found in T4 phage Hp17 mutants, and was produced in recombination-deficient Escherichia coli.
View Article and Find Full Text PDFIntervirology
May 1992
Institut für Genetik und Mikrobiologie, Universität München, BRD.
Two different DNA fragments, deriving from the P22-related bacteriophage LP7 and from the right IS element of transposon Tn10, have been identified which were recognized by the P22-packaging apparatus as pac-like signals. Their nucleotide sequences were compared with the known sequence of P22 gene 3 which contains the P22 pac site. Both sequences show similarity to a particular segment of P22 DNA close to a region identified earlier as part of pac.
View Article and Find Full Text PDFThe T1 pac site has been cloned into a plasmid vector. This recombinant plasmid was tested for T1-mediated transduction efficiency in comparison with a plasmid containing the phage lambda T1-pac-like site esp-lambda, plasmids containing T1 sequences other than the pac site, and plasmids containing neither T1 sequences nor known pac sites. The data obtained indicate that there are at least two distinct mechanisms of T1-mediated plasmid transduction.
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