Phenotypic and genetic characterization of the Bacteriophage abortive infection mechanism AbiK from Lactococcus lactis

The natural plasmid pSRQ800 isolated from Lactococcus lactis subsp. lactis W1 conferred strong phage resistance against small isometric phages of the 936 and P335 species when introduced into phage-sensitive L. lactis strains. It had very limited effect on prolate phages of the c2 species. The phage...

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Veröffentlicht in:Applied and Environmental Microbiology 1997-04, Vol.63 (4), p.1274-1283
Hauptverfasser: Emond, E. (Universite Laval, Quebec, Canada.), Holler, B.J, Boucher, I, Vandenbergh, P.A, Vedamuthu, E.R, Kondo, J.K, Moineau, S
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Sprache:eng
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Zusammenfassung:The natural plasmid pSRQ800 isolated from Lactococcus lactis subsp. lactis W1 conferred strong phage resistance against small isometric phages of the 936 and P335 species when introduced into phage-sensitive L. lactis strains. It had very limited effect on prolate phages of the c2 species. The phage resistance mechanism encoded on pSRQ800 is a temperature-sensitive abortive infection system (Abi). Plasmid pSRQ800 was mapped, and the Abi genetic determinant was localized on a 4.5-kb EcoRI fragment. Cloning and sequencing of the 4.5-kb fragment allowed the identification of two large open reading frames. Deletion mutants showed that only orfl was needed to produce the Abi phenotype. orfl (renamed abiK) coded for a predicted protein of 599 amino acids (AbiK) with an estimated molecular size of 71.4 kDa and a pI of 7.98. DNA and protein sequence alignment programs found no significant homology with databases. However, a database query based on amino acid composition suggested that AbiK might be in the same protein family as AbiA. No phage DNA replication nor phage structural protein production was detected in infected AbiK+ L. lactis cells. This system is believed to act at or prior to phage DNA replication. When cloned into a high-copy vector, AbiK efficiency increased 100 fold. AbiK provides another powerful tool that can be useful in controlling phages during lactococcal fermentations
ISSN:0099-2240
1098-5336
DOI:10.1128/aem.63.4.1274-1283.1997