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Volume 10, Number 10—October 2004
Letter

Boiling and Bacillus Spores

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To the Editor: Public health authorities rely upon “boil water” advisories to alert consumers if a potable water supply is deemed unsuitable for consumption. Holding water at a rolling boil for 1 minute will inactivate waterborne pathogens, including encysted protozoa (13). Spores of Bacillus anthracis, the agent that causes anthrax, are one of the microorganisms most refractory to inactivation by the boiling water method. This study was conducted to determine the resistance of spores of B. anthracis Sterne and three other strains of Bacillus spp. in boiling water.

B. anthracis Sterne (Colorado Serum Co., Denver, CO) was grown on soil extract peptone beef extract medium (4). Spores were harvested from the agar plates and washed four times by centrifugation with sterile distilled water, treated with 50% (vol/vol) ethanol while being shaken at 100 rpm for 2 h, then washed an additional four times by centrifugation with sterile distilled water. Spores of one of the B. cereus strains were obtained from a commercial source (Raven Biological Laboratories, Omaha, NE). Spores were produced in broth cultures for the other Bacillus spp. The second B. cereus (ATCC 9592) was grown in a generic sporulation medium (5), and B. thuringiensis var. israelensis (ATCC 35646) was grown in Schaefer’s medium (6). Spores were purified by gradient separation using RenoCal-76 (Bracco Diagnostics, Princeton, NJ) (6). Spore preparations were stored in 40% (vol/vol) ethanol at 5°C until used.

Duplicate experiments for each species were conducted in 1-L glass beakers containing 500 mL of municipal drinking water (21±2°C, pH 8.2±0.5, free available chlorine 0.5±0.3 mg/L). The beakers were left uncovered or covered with a watch glass. Steam was allowed to escape from the covered beakers through the mouth of the pouring spout. Water samples were injected with the spore preparations, heated to boiling on a hot plate, and held at boiling temperature for various times. Measuring the boiling times began when the sample reached a rolling boil. A thermocouple thermometer (Cole-Parmer, Vernon Hills, IL) directly above the liquid-air interface determined the air temperature above the boiling water after 5 min of exposure. At the conclusion of the various boiling times, the samples were removed from the heat source and allowed to cool at room temperature before analysis. These samples contained <0.2 mg/L of free available chlorine. Decimal dilutions of the water samples were analyzed in triplicate by the membrane filter procedure with nutrient agar (7).

Spores of all strains of the Bacillus spp. analyzed in this study were inactivated after boiling for 3–5 min in a covered vessel (Table). Spores still survived after 5 min of boiling in an open vessel for all of the Bacillus spp. Temperatures immediately above the surface of the boiling water in the covered vessels averaged 98.9°C, while the temperature immediately above the water level in the uncovered vessels averaged 77.3°C.

In a comprehensive literature review citing published reports dating back to 1882, Murray (8) noted that boiling times reported to destroy B. anthracis spores varied over a range of 1 to 12 min. In his own study of 17 strains of B. anthracis, Murray (8) found that boiling times of 5 to 10 min were required to achieve inactivation. Stein and Rogers (9) reported that vigorous boiling for 3 to 5 min destroyed spores from 43 strains of B. anthracis.

In our study, boiling water in a covered vessel for 3 to 5 min destroyed spores of the Bacillus spp. by greater than four orders of magnitude. Boiling for 5 min in an uncovered vessel was not as effective as boiling in a covered vessel and allowed all Bacillus spp. spores to survive. On the basis of the initial levels of spores used in this study, holding water at a rolling boil for 1–3 min in an open container would not inactivate the spores. Boiling time refers to the total time the water is held at a rolling boil and should not be confused with the first sign of bubbles from dissolved gases in the water. Since water boils at lower temperatures at higher altitudes (approximately 90°C at 3 km), boiling times must also compensate for decreased atmospheric pressure conditions (1,2).

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Eugene W. Rice*Comments to Author , Laura J. Rose†, Clifford H. Johnson*, Laura A. Boczek*, Matthew J. Arduino†, and Donald J. Reasoner*

Author affiliations: *U.S. Environmental Protection Agency, Cincinnati, Ohio, USA; †U.S. Centers for Disease Control and Prevention, Atlanta, Georgia, USA

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References

  1. Assessment of inadequately filtered public drinking water—Washington, D.C., December, 1993. MMWR Morb Mortal Week Rep. 1994;43:6619.
  2. Geldreich  EE. Drinking water microbiology—new directions toward water quality enhancement. Int J Food Microbiol. 1989;9:295312. DOIPubMed
  3. Fayer  R. Effect of high temperature on infectivity of Cryptosporidium parvum oocysts in water. Appl Environ Microbiol. 1994;60:27325.PubMed
  4. Atlas  RM. Handbook of microbiological media. 2nd ed. New York: CRC Press; 1997.
  5. Coroller  L, Leguerinel  I, Mafart  P. Effect of water activities on heating and recovery media on apparent heat resistance of Bacillus cereus spores. Appl Environ Microbiol. 2001;67:31722. DOIPubMed
  6. Nicolson  WL, Setlow  P. Sporulation, germination and outgrowth. In: CR Harwood, SM Cutting, editors. Molecular biology methods for Bacillus. New York: John Wiley & Sons; 1990. p. 391–429.
  7. Rice  EW, Fox  KR, Miltner  RJ, Lytle  DA, Johnson  CH. Evaluating plant performance using endospores. J Am Water Works Assoc. 1997;89:11220.PubMed
  8. Murray  TJ. Thermal death point II. spores of Bacillus anthracis. J Infect Dis. 1931;48:45767. DOI
  9. Stein  CD, Rogers  H. Observations on the resistance of anthrax spores to heat. Vet Med. 1945;50:40610.PubMed

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DOI: 10.3201/eid1010.040158

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Table of Contents – Volume 10, Number 10—October 2004

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Eugene W. Rice, U.S. Environmental Protection Agency, 26 W. M.L. King Dr., Cincinnati, OH 45268, USA; fax: 513-487-2555

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Page created: April 11, 2011
Page updated: April 11, 2011
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The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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