Skip to main content
Genome Announcements logoLink to Genome Announcements
. 2013 Mar 14;1(2):e00043-13. doi: 10.1128/genomeA.00043-13

Complete Genome Sequence of Escherichia Phage ADB-2 Isolated from a Fecal Sample of Poultry

D V Bhensdadia a, H D Bhimani b, C M Rawal c, V V Kothari b, V H Raval b, C R Kothari c, A B Patel d, V D Bhatt d, N R Parmar d, M R Sajnani d, P G Koringa d, C G Joshi d, S P Singh b, R K Kothari a,
PMCID: PMC3622963  PMID: 23516186

Abstract

Escherichia phage ADB-2 was isolated from a chicken fecal sample. It is a virulent phage and shows effective inhibition of Escherichia coli strains. Here we announce the completely sequenced genome of Escherichia phage ADB-2, and major findings from its annotation are described.

GENOME ANNOUNCEMENT

Escherichia coli is an opportunistic pathogen in poultry. With the rapid emergence of antibiotic-resistant bacteria, the use of bacteriophages has regained attention as an efficient alternative method for their control (1, 2). Virulent phages cause bacterial host cell lysis and not only function to control bacterial populations but also can be used as indicators of bacterial (fecal) contamination (3, 4) and as tools for identifying (typing) specific bacterial strains (5, 6). Poultry meat is one of the most popular foods. Poultry and poultry meat are often found to be contaminated with potentially pathogenic microorganisms. Improvements in biosecurity on poultry farms are likely to be very expensive and difficult to maintain (7), so there is a need to find an acceptable, cost-effective way of preventing infection of poultry with coliform bacteria (8).

Escherichia phage ADB-2 was isolated from a fecal sample of poultry by the double-layer agar plaque method. The Spot test (9) and DAL method were used to determine the host range of the Escherichia phage ADB-2. An antibiogram of the natural host of Escherichia phage ADB-2 showed that the host was sensitive against norfloxacin and gentamicin and that it demonstrated higher resistance against cotrimoxazole and oxytetracycline (data not shown). Escherichia phage ADB-2 was purified by ultracentrifugation and by the CsCl2 density gradient purification method. Genomic DNA was extracted from the stock by the alkaline lysis method. The whole-genome sequencing of Escherichia phage ADB-2 was performed using Ion Torrent PGM (Ion 200-bp sequencing kit) (Life Technologies).

The data generated from the genomic library contained 229,781 reads and 45,496,800 nucleotide bases with average read length of 198 bases. The assembly using Newbler version 2.6 generated a 50,552-bp-long single chromosome. The genome annotation and comparative analysis of the genome were done using Rapid Annotation using Subsystem Technology (RAST) (10). The phage has 46% GC with 76 predicted coding regions and 2 RNA genes.

This genome contains functional genes related to phage structure and packaging machinery (major capsid protein, unknown phage structure proteins, and terminase), phage neck protein, tail structure for host interaction (tail fiber protein, tail sheath protein, and tail-associated protein), phage DNA synthesis (helicase, DNA-directed RNA polymerases, endoDNase, and transcription regulator) and host lysis (endolysin without holin). These functional genes are scattered over the genome. The complete genome analysis of this phage provides new insight into its characteristics and interactions with Escherichia coli.

Nucleotide sequence accession number.

The complete sequence of the Escherichia phage ADB-2 genome can be accessed under the GenBank accession number JX912252.1.

ACKNOWLEDGMENT

The project was funded by Dhimant V. Bhensdadia under his Post Graduate Research Programme.

Footnotes

Citation Bhensdadia DV, Bhimani HD, Rawal CM, Kothari VV, Raval VH, Kothari CR, Patel AB, Bhatt VD, Parmar NR, Sajnani MR, Koringa PG, Joshi CG, Singh SP, Kothari RK. 2013. Complete genome sequence of Escherichia phage ADB-2 isolated from a fecal sample of poultry. Genome Announc. 1(2):e00043-13. doi:10.1128/genomeA.00043-13.

REFERENCES

  • 1. Hagens S, Loessner MJ. 2007. Application of bacteriophages for detection and control of foodborne pathogens. Appl. Microbiol. Biotechnol. 76:513–519 [DOI] [PubMed] [Google Scholar]
  • 2. Matsuzaki S, Rashel M, Uchiyama J, Sakurai S, Ujihara T, Kuroda M, Ikeuchi M, Tani T, Fujieda M, Wakiguchi H, Imai S. 2005. Bacteriophage therapy: a revitalized therapy against bacterial infectious diseases. J. Infect. Chemother. 11:211–219 [DOI] [PubMed] [Google Scholar]
  • 3. Miller AJ, Eblen BS, Oser A, Burkhardt W., III 1998. Application and evaluation of male-specific bacteriophage as a process integrity or faecal contamination indicator in a pork slaughterhouse. J. Appl. Microbiol. 85:898–904 [DOI] [PubMed] [Google Scholar]
  • 4. Tanji Y, Mizoguchi K, Yoichi M, Morita M, Kijima N, Kator H, Unno H. 2003. Seasonal change and fate of coliphages infected to Escherichia coli O157:H7 in a wastewater treatment plant. Water Res. 37:1136–1142 [DOI] [PubMed] [Google Scholar]
  • 5. Sinton LW, Finlay RK, Hannah DJ. 1998. Distinguishing human from animal faecal contamination in water: a review. N. Z. J. Mar. Freshw. Res. 32:323–348 [Google Scholar]
  • 6. Welkos S, Schreiber M, Baer H. 1974. Identification of salmonella with the O-1 bacteriophage. Appl. Microbiol. 28:618–622 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Davies RH. 2005. Pathogen populations on poultry farms, p 101–135 In Mead G, Food safety control in the poultry industry. Woodhead Publishing, Cambridge, United Kingdom [Google Scholar]
  • 8. Atterbury RJ, Van Bergen MAP, Ortiz F, Lovell MA, Harris JA, De Boer A, Wagenaar JA, Allen VM, Barrow PA. 2007. Bacteriophage therapy to reduce salmonella colonization of broiler chickens. Appl. Environ. Microbiol. 73:4543–4549 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Champagne NG. 1995. The spot test method for the in-plant enumeration of bacteriophages with paired cultures of Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus salivarius subsp. thermophilus. Int. Dairy J. 5:417–425 [Google Scholar]
  • 10. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, Formsma K, Gerdes S, Glass EM, Kubal M, Meyer F, Olsen GJ, Olson R, Osterman AL, Overbeek RA, McNeil LK, Paarmann D, Paczian T, Parrello B, Pusch GD, Reich C, Stevens R, Vassieva O, Vonstein V, Wilke A, Zagnitko O. 2008. The RAST server: rapid annotations using subsystems technology. BMC Genomics 9:75 [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genome Announcements are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES