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. 1997 May;179(9):2949–2957. doi: 10.1128/jb.179.9.2949-2957.1997

Molecular characterization of a genomic region in a Lactococcus bacteriophage that is involved in its sensitivity to the phage defense mechanism AbiA.

P K Dinsmore 1, T R Klaenhammer 1
PMCID: PMC179059  PMID: 9139913

Abstract

A spontaneous mutant of the lactococcal phage phi31 that is insensitive to the phage defense mechanism AbiA was characterized in an effort to identify the phage factor(s) involved in sensitivity of phi31 to AbiA. A point mutation was localized in the genome of the AbiA-insensitive phage (phi31A) by heteroduplex analysis of a 9-kb region. The mutation (G to T) was within a 738-bp open reading frame (ORF245) and resulted in an arginine-to-leucine change in the predicted amino acid sequence of the protein. The mutant phi31A-ORF245 reduced the sensitivity of phi31 to AbiA when present in trans, indicating that the mutation in ORF245 is responsible for the AbiA insensitivity of phi31A. Transcription of ORF245 occurs early in the phage infection cycles of phi31 and phi31A and is unaffected by AbiA. Expansion of the phi31 sequence revealed ORF169 (immediately upstream of ORF245) and ORF71 (which ends 84 bp upstream of ORF169). Two inverted repeats lie within the 84-bp region between ORF71 and ORF169. Sequence analysis of an independently isolated AbiA-insensitive phage, phi31B, identified a mutation (G to A) in one of the inverted repeats. A 118-bp fragment from phi31, encompassing the 84-bp region between ORF71 and ORF169, eliminates AbiA activity against phi31 when present in trans, establishing a relationship between AbiA and this fragment. The study of this region of phage phi31 has identified an open reading frame (ORF245) and a 118-bp DNA fragment that interact with AbiA and are likely to be involved in the sensitivity of this phage to AbiA.

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Selected References

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  1. Alatossava T., Klaenhammer T. R. Molecular Characterization of Three Small Isometric-Headed Bacteriophages Which Vary in Their Sensitivity to the Lactococcal Phage Resistance Plasmid pTR2030. Appl Environ Microbiol. 1991 May;57(5):1346–1353. doi: 10.1128/aem.57.5.1346-1353.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  3. Amitsur M., Morad I., Chapman-Shimshoni D., Kaufmann G. HSD restriction-modification proteins partake in latent anticodon nuclease. EMBO J. 1992 Aug;11(8):3129–3134. doi: 10.1002/j.1460-2075.1992.tb05385.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Anba J., Bidnenko E., Hillier A., Ehrlich D., Chopin M. C. Characterization of the lactococcal abiD1 gene coding for phage abortive infection. J Bacteriol. 1995 Jul;177(13):3818–3823. doi: 10.1128/jb.177.13.3818-3823.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bidnenko E., Ehrlich D., Chopin M. C. Phage operon involved in sensitivity to the Lactococcus lactis abortive infection mechanism AbiD1. J Bacteriol. 1995 Jul;177(13):3824–3829. doi: 10.1128/jb.177.13.3824-3829.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Boyce J. D., Davidson B. E., Hillier A. J. Sequence analysis of the Lactococcus lactis temperate bacteriophage BK5-T and demonstration that the phage DNA has cohesive ends. Appl Environ Microbiol. 1995 Nov;61(11):4089–4098. doi: 10.1128/aem.61.11.4089-4098.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Budowle B., Chakraborty R., Giusti A. M., Eisenberg A. J., Allen R. C. Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE. Am J Hum Genet. 1991 Jan;48(1):137–144. [PMC free article] [PubMed] [Google Scholar]
  8. Chandry P. S., Davidson B. E., Hillier A. J. Temporal transcription map of the Lactococcus lactis bacteriophage sk1. Microbiology. 1994 Sep;140(Pt 9):2251–2261. doi: 10.1099/13500872-140-9-2251. [DOI] [PubMed] [Google Scholar]
  9. Chen M., Pan Z. Q., Hurwitz J. Studies of the cloned 37-kDa subunit of activator 1 (replication factor C) of HeLa cells. Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5211–5215. doi: 10.1073/pnas.89.12.5211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Cluzel P. J., Chopin A., Ehrlich S. D., Chopin M. C. Phage abortive infection mechanism from Lactococcus lactis subsp. lactis, expression of which is mediated by an Iso-ISS1 element. Appl Environ Microbiol. 1991 Dec;57(12):3547–3551. doi: 10.1128/aem.57.12.3547-3551.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Coffey A. G., Fitzgerald G. F., Daly C. Cloning and characterization of the determinant for abortive infection of bacteriophage from lactococcal plasmid pCI829. J Gen Microbiol. 1991 Jun;137(6):1355–1362. doi: 10.1099/00221287-137-6-1355. [DOI] [PubMed] [Google Scholar]
  12. Cram D., Ray A., Skurray R. Molecular analysis of F plasmid pif region specifying abortive infection of T7 phage. Mol Gen Genet. 1984;197(1):137–142. doi: 10.1007/BF00327934. [DOI] [PubMed] [Google Scholar]
  13. Dao M. L., Ferretti J. J. Streptococcus-Escherichia coli shuttle vector pSA3 and its use in the cloning of streptococcal genes. Appl Environ Microbiol. 1985 Jan;49(1):115–119. doi: 10.1128/aem.49.1.115-119.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Dinsmore P. K., Klaenhammer T. R. Phenotypic Consequences of Altering the Copy Number of abiA, a Gene Responsible for Aborting Bacteriophage Infections in Lactococcus lactis. Appl Environ Microbiol. 1994 Apr;60(4):1129–1136. doi: 10.1128/aem.60.4.1129-1136.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Dubiel W., Ferrell K., Pratt G., Rechsteiner M. Subunit 4 of the 26 S protease is a member of a novel eukaryotic ATPase family. J Biol Chem. 1992 Nov 15;267(32):22699–22702. [PubMed] [Google Scholar]
  16. Duckworth D. H., Glenn J., McCorquodale D. J. Inhibition of bacteriophage replication by extrachromosomal genetic elements. Microbiol Rev. 1981 Mar;45(1):52–71. doi: 10.1128/mr.45.1.52-71.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Durmaz E., Higgins D. L., Klaenhammer T. R. Molecular characterization of a second abortive phage resistance gene present in Lactococcus lactis subsp. lactis ME2. J Bacteriol. 1992 Nov;174(22):7463–7469. doi: 10.1128/jb.174.22.7463-7469.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Fry D. C., Kuby S. A., Mildvan A. S. ATP-binding site of adenylate kinase: mechanistic implications of its homology with ras-encoded p21, F1-ATPase, and other nucleotide-binding proteins. Proc Natl Acad Sci U S A. 1986 Feb;83(4):907–911. doi: 10.1073/pnas.83.4.907. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Garvey P., Fitzgerald G. F., Hill C. Cloning and DNA sequence analysis of two abortive infection phage resistance determinants from the lactococcal plasmid pNP40. Appl Environ Microbiol. 1995 Dec;61(12):4321–4328. doi: 10.1128/aem.61.12.4321-4328.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Gasson M. J. Plasmid complements of Streptococcus lactis NCDO 712 and other lactic streptococci after protoplast-induced curing. J Bacteriol. 1983 Apr;154(1):1–9. doi: 10.1128/jb.154.1.1-9.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hanahan D. Studies on transformation of Escherichia coli with plasmids. J Mol Biol. 1983 Jun 5;166(4):557–580. doi: 10.1016/s0022-2836(83)80284-8. [DOI] [PubMed] [Google Scholar]
  22. Hill C., Massey I. J., Klaenhammer T. R. Rapid method to characterize lactococcal bacteriophage genomes. Appl Environ Microbiol. 1991 Jan;57(1):283–288. doi: 10.1128/aem.57.1.283-288.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Hill C., Miller L. A., Klaenhammer T. R. Nucleotide sequence and distribution of the pTR2030 resistance determinant (hsp) which aborts bacteriophage infection in lactococci. Appl Environ Microbiol. 1990 Jul;56(7):2255–2258. doi: 10.1128/aem.56.7.2255-2258.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Hill C., Pierce K., Klaenhammer T. R. The conjugative plasmid pTR2030 encodes two bacteriophage defense mechanisms in lactococci, restriction modification (R+/M+) and abortive infection (Hsp+). Appl Environ Microbiol. 1989 Sep;55(9):2416–2419. doi: 10.1128/aem.55.9.2416-2419.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Hill C., Romero D. A., McKenney D. S., Finer K. R., Klaenhammer T. R. Localization, cloning, and expression of genetic determinants for bacteriophage resistance (Hsp) from the conjugative plasmid pTR2030. Appl Environ Microbiol. 1989 Jul;55(7):1684–1689. doi: 10.1128/aem.55.7.1684-1689.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Holo H., Nes I. F. High-Frequency Transformation, by Electroporation, of Lactococcus lactis subsp. cremoris Grown with Glycine in Osmotically Stabilized Media. Appl Environ Microbiol. 1989 Dec;55(12):3119–3123. doi: 10.1128/aem.55.12.3119-3123.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Jarvis A. W., Klaenhammer T. R. Bacteriophage Resistance Conferred on Lactic Streptococci by the Conjugative Plasmid pTR2030: Effects on Small Isometric-, Large Isometric-, and Prolate-Headed Phages. Appl Environ Microbiol. 1986 Jun;51(6):1272–1277. doi: 10.1128/aem.51.6.1272-1277.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Kao C., Snyder L. The lit gene product which blocks bacteriophage T4 late gene expression is a membrane protein encoded by a cryptic DNA element, e14. J Bacteriol. 1988 May;170(5):2056–2062. doi: 10.1128/jb.170.5.2056-2062.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Levitz R., Chapman D., Amitsur M., Green R., Snyder L., Kaufmann G. The optional E. coli prr locus encodes a latent form of phage T4-induced anticodon nuclease. EMBO J. 1990 May;9(5):1383–1389. doi: 10.1002/j.1460-2075.1990.tb08253.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Li X., Burgers P. M. Molecular cloning and expression of the Saccharomyces cerevisiae RFC3 gene, an essential component of replication factor C. Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):868–872. doi: 10.1073/pnas.91.3.868. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Lubbers M. W., Waterfield N. R., Beresford T. P., Le Page R. W., Jarvis A. W. Sequencing and analysis of the prolate-headed lactococcal bacteriophage c2 genome and identification of the structural genes. Appl Environ Microbiol. 1995 Dec;61(12):4348–4356. doi: 10.1128/aem.61.12.4348-4356.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. McLandsborough L. A., Kolaetis K. M., Requena T., McKay L. L. Cloning and characterization of the abortive infection genetic determinant abiD isolated from pBF61 of Lactococcus lactis subsp. lactis KR5. Appl Environ Microbiol. 1995 May;61(5):2023–2026. doi: 10.1128/aem.61.5.2023-2026.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Moineau S., Pandian S., Klaenhammer T. R. Evolution of a Lytic Bacteriophage via DNA Acquisition from the Lactococcus lactis Chromosome. Appl Environ Microbiol. 1994 Jun;60(6):1832–1841. doi: 10.1128/aem.60.6.1832-1841.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Molineux I. J., Schmitt C. K., Condreay J. P. Mutants of bacteriophage T7 that escape F restriction. J Mol Biol. 1989 Jun 5;207(3):563–574. doi: 10.1016/0022-2836(89)90465-8. [DOI] [PubMed] [Google Scholar]
  35. Murgola E. J., Guarneros G. Ribosomal RNA and peptidyl-tRNA hydrolase: a peptide chain termination model for lambda bar RNA inhibition. Biochimie. 1991 Dec;73(12):1573–1578. doi: 10.1016/0300-9084(91)90193-5. [DOI] [PubMed] [Google Scholar]
  36. Möller W., Amons R. Phosphate-binding sequences in nucleotide-binding proteins. FEBS Lett. 1985 Jul 1;186(1):1–7. doi: 10.1016/0014-5793(85)81326-0. [DOI] [PubMed] [Google Scholar]
  37. O'Sullivan D. J., Klaenhammer T. R. High- and low-copy-number Lactococcus shuttle cloning vectors with features for clone screening. Gene. 1993 Dec 31;137(2):227–231. doi: 10.1016/0378-1119(93)90011-q. [DOI] [PubMed] [Google Scholar]
  38. O'Sullivan D. J., Walker S. A., West S. G., Klaenhammer T. R. Development of an expression strategy using a lytic phage to trigger explosive plasmid amplification and gene expression. Biotechnology (N Y) 1996 Jan;14(1):82–87. doi: 10.1038/nbt0196-82. [DOI] [PubMed] [Google Scholar]
  39. O'Sullivan D. J., Zagula K., Klaenhammer T. R. In vivo restriction by LlaI is encoded by three genes, arranged in an operon with llaIM, on the conjugative Lactococcus plasmid pTR2030. J Bacteriol. 1995 Jan;177(1):134–143. doi: 10.1128/jb.177.1.134-143.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. O'sullivan D. J., Hill C., Klaenhammer T. R. Effect of Increasing the Copy Number of Bacteriophage Origins of Replication, in trans, on Incoming-Phage Proliferation. Appl Environ Microbiol. 1993 Aug;59(8):2449–2456. doi: 10.1128/aem.59.8.2449-2456.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. O'sullivan D. J., Klaenhammer T. R. Rapid Mini-Prep Isolation of High-Quality Plasmid DNA from Lactococcus and Lactobacillus spp. Appl Environ Microbiol. 1993 Aug;59(8):2730–2733. doi: 10.1128/aem.59.8.2730-2733.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Parma D. H., Snyder M., Sobolevski S., Nawroz M., Brody E., Gold L. The Rex system of bacteriophage lambda: tolerance and altruistic cell death. Genes Dev. 1992 Mar;6(3):497–510. doi: 10.1101/gad.6.3.497. [DOI] [PubMed] [Google Scholar]
  43. Parreira R., Ehrlich S. D., Chopin M. C. Dramatic decay of phage transcripts in lactococcal cells carrying the abortive infection determinant AbiB. Mol Microbiol. 1996 Jan;19(2):221–230. doi: 10.1046/j.1365-2958.1996.371896.x. [DOI] [PubMed] [Google Scholar]
  44. Raya R. R., Kleeman E. G., Luchansky J. B., Klaenhammer T. R. Characterization of the temperate bacteriophage phi adh and plasmid transduction in Lactobacillus acidophilus ADH. Appl Environ Microbiol. 1989 Sep;55(9):2206–2213. doi: 10.1128/aem.55.9.2206-2213.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Sanders M. E., Klaenhammer T. R. Characterization of Phage-Sensitive Mutants from a Phage-Insensitive Strain of Streptococcus lactis: Evidence for a Plasmid Determinant that Prevents Phage Adsorption. Appl Environ Microbiol. 1983 Nov;46(5):1125–1133. doi: 10.1128/aem.46.5.1125-1133.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Spicer E. K., Nossal N. G., Williams K. R. Bacteriophage T4 gene 44 DNA polymerase accessory protein. Sequences of gene 44 and its protein product. J Biol Chem. 1984 Dec 25;259(24):15425–15432. [PubMed] [Google Scholar]
  48. Sutherland E., Coe L., Raleigh E. A. McrBC: a multisubunit GTP-dependent restriction endonuclease. J Mol Biol. 1992 May 20;225(2):327–348. doi: 10.1016/0022-2836(92)90925-a. [DOI] [PubMed] [Google Scholar]
  49. Terzaghi B. E., Sandine W. E. Improved medium for lactic streptococci and their bacteriophages. Appl Microbiol. 1975 Jun;29(6):807–813. doi: 10.1128/am.29.6.807-813.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Yanisch-Perron C., Vieira J., Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103–119. doi: 10.1016/0378-1119(85)90120-9. [DOI] [PubMed] [Google Scholar]
  51. Yu Y. T., Snyder L. Translation elongation factor Tu cleaved by a phage-exclusion system. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):802–806. doi: 10.1073/pnas.91.2.802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Zhu K. Y., Clark J. M. Rapid construction of nested deletions of recombinant plasmid DNA for dideoxy sequencing. Biotechniques. 1995 Feb;18(2):222–224. [PubMed] [Google Scholar]

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