Abstract

The number of successful propagations/isolations of soil-borne bacteriophages is small in comparison to the number of bacteriophages observed by microscopy (great plaque count anomaly). As one resolution of the great plaque count anomaly, we use propagation in ultra-dilute agarose gels to isolate a Bacillus thuringiensis bacteriophage with a large head (95 nm in diameter), tail (486 × 26 nm), corkscrew-like tail fibers (187 × 10 nm) and genome (221 Kb) that cannot be detected by the usual procedures of microbiology. This new bacteriophage, called 0305φ8-36 (first number is month/year of isolation; remaining two numbers identify the host and bacteriophage), has a high dependence of plaque size on the concentration of a supporting agarose gel. Bacteriophage 0305φ8-36 does not propagate in the traditional gels used for bacteriophage plaque formation and also does not produce visible lysis of liquid cultures. Bacteriophage 0305φ8-36 aggregates and, during de novo isolation from the environment, is likely to be invisible to procedures of physical detection that use either filtration or centrifugal pelleting to remove bacteria. Bacteriophage 0305φ8-36 is in a new genomic class, based on genes for both structural components and DNA packaging ATPase. Thus, knowledge of environmental virus diversity is expanded with prospect of greater future expansion.

Highlights

  • Current data indicate that roughly 1031 bacteriophages exist worldwide, including about 108 genotypes and possibly most of the earth's gene diversity [1,2,3,4]

  • Less than 1% of the observed bacteriophages have ever been grown in culture

  • The great plaque count anomaly is especially dramatic in the case of soilborne bacteriophages

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Summary

Introduction

Current data indicate that roughly 1031 bacteriophages exist worldwide, including about 108 genotypes and possibly most of the earth's gene diversity [1,2,3,4]. Propagated bacteriophages are sometimes not obtained from soil samples in spite of concentrations in the 108 – 109 range per gram, when detected by microscopy [5]. Fluorescence microscopy of material removed from plaques reveals that aggregation occurs during growth (not shown).

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