Abstract
A proposed new genus of the family Myoviridae, “rV5-like viruses”, includes two lytic bacteriophages: Escherichia coli O157: H7-specific bacteriophage rV5 and Salmonella phage PVP-SE1. Here, we present basic properties and genomic characterization of a novel rV5-like phage, vB_EcoM_FV3, which infects E. coli K-12-derived laboratory strains and replicates at high temperature (up to 47 °C). The 136,947-bp genome of vB_EcoM_FV3 contains 218 open reading frames and encodes 5 tRNAs. The genomic content and organization of vB_EcoM_FV3 is more similar to that of rV5 than to PVP-SE1, but all three phages share similar morphological characteristics and form a homogeneous phage group.
References
Hatfull GF (2008) Bacteriophage genomics. Curr Opin Microbiol 11:447–453. doi:10.1016/j.mib.2008.09.004
Lavigne R, Seto D, Mahadevan P, Ackermann H-W, Kropinski AM (2008) Unifying classical and molecular taxonomic classification: analysis of the Podoviridae using BLASTP-based tools. Res Microbiol 159:406–414. doi:10.1016/j.resmic.2008.03.005
Lavigne R, Darius P, Summer EJ, Seto D, Mahadevan P, Nilsson AS, Ackerman HW, Kropinski AM (2009) Classification of Myoviridae bacteriophages using protein sequence similarity. BMC Microbiol 9:224. doi:10.1186/1471-2180-9-224
Santos SB, Kropinski AM, Ceyssens P-J, Ackermann H-W, Villegas A, Lavigne R, Krylov VN, Carvalho CM, Ferreira EC, Azeredo J (2011) Genomic and proteomic characterization of the broad host range Salmonella phage PVP-SE1: the creation of a new phage genus. J Virol 85:11265–11273. doi:10.1128/JVI.01769-10
Santos SB, Fernandes E, Carvalho CM, Sillankorva S, Krylov VN, Pleteneva EA, Shaburova OV, Nicolau A, Ferreira EC, Azeredo J (2010) Selection and characterization of a multivalent Salmonella phage and its production in a nonpathogenic Escherichia coli strain. Appl Environ Microbiol 76:7338–7342. doi:10.1128/AEM.00922-10
Niu YD, Johnson RP, Xu Y, McAllister TA, Sharma R, Louie M, Stanford K (2009) Host range and lytic capability of four bacteriophages against bovine and clinical human isolates of Shiga toxin-producing Escherichia coli O157:H7. J Appl Microbiol 107:646–656. doi:10.1111/j.1365-2672.2009.04231.x
Stanford K, McAllister TA, Niu YD, Stephens TP, Mazzocco A, Waddell TE, Johnson RP (2010) Oral delivery systems for encapsulated bacteriophages targeted at Escherichia coli O157:H7 in feedlot cattle. J Food Prot 73:1304–1312
Carlson K, Miller E (1994) Experiments in T4 genetics. In: Karam JD (ed) Molecular biology of bacteriophage T4. ASM Press, Washington DC, pp 419–483
Carver T, Berriman M, Tivey A, Patel C, Böhme U, Barrell BG, Parkhill J, Rajandream M-A (2008) Artemis and ACT: viewing, annotating and comparing sequences stored in a relational database. Bioinformatics 24:2672–2676. doi:10.1093/bioinformatics/btn529
Veluchamy A, Mary S, Acharya V, Mehta P, Deva T, Krishnaswamy S (2009) HNHDb: A database on pattern based classification of HNH domains reveals functional relevance of sequence patterns and domain associations. Bioinformation 4:80–83
Scholl D, Rogers S, Adhya S, Merril CR (2001) Bacteriophage K1–5 encodes two different tail fiber proteins, allowing it to infect and replicate on both K1 and K5 strains of Escherichia coli. J Virol 75:2509–2515. doi:10.1128/JVI.75.6.2509-2515.2001
Yoichi M, Abe M, Miyanaga K, Unno H, Tanji Y (2005) Alteration of tail fiber protein gp38 enables T2 phage to infect Escherichia coli O157:H7. J Biotechnol 115:101–107. doi:10.1016/j.jbiotec.2004.08.003
Morita M, Fischer CR, Mizoguchi K, Yoichi M, Oda M, Tanji Y, Unno H (2002) Amino acid alterations in Gp38 of host range mutants of PP01 and evidence for their infection of an ompC null mutant of Escherichia coli O157:H7. FEMS Microbiol Lett 216:243–248
Bollback JP, Huelsenbeck JP (2009) Parallel genetic evolution within and between bacteriophage species of varying degrees of divergence. Genetics 181:225–234. doi:10.1534/genetics.107.085225
Brown CJ, Zhao L, Evans KJ, Ally D, Stancik AD (2010) Positive selection at high temperature reduces gene transcription in the bacteriophage ϕX174. BMC Evol Biol 10:378. doi:10.1186/1471-2148-10-378
Tenaillon O, Rodrίguez-Verdugo A, Gaut RL, McDonald P, Bennett AF, Long AD, Gaut BS (2012) The molecular diversity of adaptive convergence. Science 335:457–461. doi:10.1126/science.1212986
Friman V-P, Hiltunen T, Jalasvuori M, Lindstedt C, Laanto E, Örmälä AM, Laakso J, Mappes J, Bamford JK (2011) High temperature and bacteriophages can indirectly select for bacterial pathogenicity in environmental reservoirs. PLoS One 6:e17651. doi:10.1371/journal.pone.0017651
Yue W-F, Du M, Zhu M-J (2012) High temperature in combination with UV irradiation enhances horizontal transfer of stx2 gene from E. coli O157:H7 to non-pathogenic E. coli. PLoS One 7:e31308. doi:10.1371/journal.pone.0031308
Wiberg JS, Mowrey-McKee MF, Stevens EJ (1988) Induction of the heat shock regulon of Escherichia coli markedly increases production of bacterial viruses at high temperatures. J Virol 62:234–245
Pitout JDD (2012) Extraintestinal pathogenic Escherichia coli: a combination of virulence with antibiotic resistance. Front Microbiol 3:9. doi:10.3389/fmicb.2012.00009
Kudva IT, Jelacic S, Tarr PI, Youderian P, Hovde CJ (1999) Biocontrol of Escherichia coli O157:H7 with O157-specific bacteriophages. Appl Environ Microbiol 65:3767–3773
Chibani-Chenoufi S, Sidoti J, Bruttin A, Kutter E, Sarker S, Brüssow H (2004) In vitro and in vivo bacteriolytic activities of Escherichia coli phages: implications for phage therapy. Antimicrob Agents Chemother 48:2558–2569. doi:10.1128/AAC.48.7.2558-2569.2004
Villegas A, She Y-M, Kropinski AM, Lingohr EJ, Mazzocco A, Ojha S, Waddell TE, Ackermann H-W, Moyles DM, Ahmed R, Johnson RP (2009) The genome and proteome of a virulent Escherichia coli O157:H7 bacteriophage closely resembling Salmonella phage Felix O1. Virol J 6:41. doi:10.1186/1743-422×-6-41
Kutter EM, Skutt-Kakaria K, Blasdel B, El-Shibiny A, Castano A, Bryan D, Kropinski AM, Villegas A, Ackermann H-W, Toribio AL, Pickard D, Anany H, Callaway T, Brabban AD (2011) Characterization of a ViI-like phage specific to Escherichia coli O157:H7. Virol J 8:430. doi:10.1186/1743-422X-8-430
Liao WC, Ng WV, Lin IH, Syu WJ, Liu TT, Chang CH (2011) T4-Like genome organization of the Escherichia coli O157:H7 lytic phage AR1J Virol 85:6567–6578. doi:10.1128/JVI.02378-10
Miller ES, Kutter E, Mosig G, Arisaka F, Kunisawa T, Rüger W (2003) Bacteriophage T4 genome. Microbiol Mol Biol Rev 67:86–156
Molineux I (2006) The T7 group. In: Calendar R (ed) The bacteriophages. Oxford University Press: New York, pp 277–301
Acknowledgments
We thank Dr. Ken Kreuzer, Dr. Victor Krylov and Dr. Lindsay W. Black for E. coli strains. This work was supported in part by the Lithuanian State Science and Studies Foundation (Grant No. N-07005) and was also funded by a grant (No. MIP-76/2010) from the Research Council of Lithuania.
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Supplementary material 1 Table 1S. A list of bacteriophage vB_EcoM_FV3 putative genes with predicted functions. (DOC 285 kb)
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Supplementary material 2 Fig. 1S. Functional genomic map of bacteriophage vB_EcoM_FV3. Putative genes with predicted coding functions are represented as arrows. The colour code for the online version of the article is as follows: yellow—DNA replication, recombination, repair and packaging; brown—transcription, translation, nucleotide metabolism; blue—virion structure; green—chaperones/assembly; purple—lysis, host or phage interactions; grey—ORFs of unknown function; red—unique FV3 ORFs of unknown function; black—tRNA. (TIFF 4748 kb)
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Truncaite, L., Šimoliūnas, E., Zajančkauskaite, A. et al. Bacteriophage vB_EcoM_FV3: a new member of “rV5-like viruses”. Arch Virol 157, 2431–2435 (2012). https://doi.org/10.1007/s00705-012-1449-x
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DOI: https://doi.org/10.1007/s00705-012-1449-x