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. 1989 Apr;55(4):912–921. doi: 10.1128/aem.55.4.912-921.1989

Nonphotosynthetic pigmented bacteria in a potable water treatment and distribution system.

D J Reasoner 1, J C Blannon 1, E E Geldreich 1, J Barnick 1
PMCID: PMC184224  PMID: 2729990

Abstract

The occurrence of pigmented bacteria in potable water, from raw source water through treatment to distribution water, including dead-end locations, was compared at sample sites in a large municipal water system. Media used to enumerate heterotrophic bacteria and differentiate pigmented colonies were standard method plate count (SPC), m-SPC, and R2A agars, incubated up to 7 days at 35 degrees C. The predominant pigmented bacteria at most sample locations were yellow and orange, with a small incidence of pink organisms at the flowing distribution site. Seasonal variations were seen, with the yellow and orange organisms shifting in dominance. SPC agar was the least productive medium for both heterotroph counts and pigmented bacteria differentiation. At the flowing distribution site, percentages of pigmented bacteria on SPC medium ranged from 2.3 to 9.67 times less than on m-SPC and from 2.3 to 9.86 times less than on R2A. At the same site, seasonal trends in the percentage of pigmented bacteria were the same for m-SPC and R2A media, and the highest and lowest percentages occurred in the fall and winter, respectively. At site 6, there appeared to be an inverse relationship between the yellow and orange pigmented groups, but upon analysis, this did not hold and all correlations between yellow and orange pigmented bacteria were positive. The study results indicate that pigmented bacteria could readily be detected by using plate counting media developed for heterotroph enumeration in potable waters with incubation periods of 7 days. Pigmented bacteria can be used as an additional marker for monitoring changes in water quality. High numbers of heterotrophs, including pigmented forms, were found at dead-end locations, usually in the absence of a free chlorine residual and when the water temperature was greater than 16 degrees C. The association of some pigmented bacteria with nosocomial and other infections raises concern that the organisms may have originated from the potable water supply. High levels of pigmented bacteria could pose an increased health risk to immunologically compromised individuals. Therefore, the bacterial quality of the distribution water should be controlled to prevent the development of high concentrations of heterotrophic plate count bacteria, including the pigmented forms.

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Selected References

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  1. CABRERA H. A., DAVIS G. H. Epidemic meningitis of the newborn caused by flavobacteria. I. Epidemiology and bacteriology. Am J Dis Child. 1961 Mar;101:289–295. doi: 10.1001/archpedi.1961.04020040017004. [DOI] [PubMed] [Google Scholar]
  2. Dott W. Qualitative und quantitative Bestimmung von Bakterienpopulationen aus aquatischen Biotopen. 6. Mitteilung: Wiederverkeimung im Trinkwasser. Zentralbl Bakteriol Mikrobiol Hyg B. 1983 Oct;178(3):263–279. [PubMed] [Google Scholar]
  3. Druce R. G., Thomas S. B. An ecological study of the psychrotrophic bacteria of soil, water, grass and hay. J Appl Bacteriol. 1970 Jun;33(2):420–435. doi: 10.1111/j.1365-2672.1970.tb02215.x. [DOI] [PubMed] [Google Scholar]
  4. Favero M. S., Petersen N. J., Boyer K. M., Carson L. A., Bond W. W. Microbial contamination of renal dialysis systems and associated health risks. Trans Am Soc Artif Intern Organs. 1974;20A:175–183. [PubMed] [Google Scholar]
  5. Favero M. S., Petersen N. J., Carson L. A., Bond W. W., Hindman S. H. Gram-negative water bacteria in hemodialysis systems. Health Lab Sci. 1975 Oct;12(4):321–334. [PubMed] [Google Scholar]
  6. Feeley T. W., Du Moulin G. C., Hedley-Whyte J., Bushnell L. S., Gilbert J. P., Feingold D. S. Aerosol polymyxin and pneumonia in seriously ill patients. N Engl J Med. 1975 Sep 4;293(10):471–475. doi: 10.1056/NEJM197509042931003. [DOI] [PubMed] [Google Scholar]
  7. Gräf W., Bauer L. Roter Bakterienaufwuchs (Corynebacterium rubrum n. spec.) in Leitungswassersystemen. Zentralbl Bakteriol Orig B. 1973 Jun;157(4):291–303. [PubMed] [Google Scholar]
  8. HERMAN L. G., HIMMELSBACH C. K. DETECTION AND CONTROL OF HOSPITAL SOURCES OF FLAVOBACTERIA. Hospitals. 1965 Jun 16;39:72–76. [PubMed] [Google Scholar]
  9. Herman L. G. Sources of the slow-growing pigmented water bacteria. Health Lab Sci. 1976 Jan;13(1):5–10. [PubMed] [Google Scholar]
  10. Holmes B., Snell J. J., Lapage S. P. Flavobacterium odoratum: a species resistant to a wide range of antimicrobial agents. J Clin Pathol. 1979 Jan;32(1):73–77. doi: 10.1136/jcp.32.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. KING E. O. Studies on a group of previously unclassified bacteria associated with meningitis in infants. Am J Clin Pathol. 1959 Mar;31(3):241–247. doi: 10.1093/ajcp/31.3.241. [DOI] [PubMed] [Google Scholar]
  12. Koburger J. A., May S. O. Isolation of Chromobacterium spp. from foods, soil, and water. Appl Environ Microbiol. 1982 Dec;44(6):1463–1465. doi: 10.1128/aem.44.6.1463-1465.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Matsen J. M. Hospital infections with pigmented water bacteria. Health Lab Sci. 1975 Oct;12(4):305–310. [PubMed] [Google Scholar]
  14. Okuda T., Endo N., Osada Y., Zen-Yoji H. Outbreak of nosocomial urinary tract infections caused by Serratia marcescens. J Clin Microbiol. 1984 Oct;20(4):691–695. doi: 10.1128/jcm.20.4.691-695.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Olsen H. Flavobacterium meningosepticum isolated from outside hospital surroundings and during routine examination of patient specimens. Acta Pathol Microbiol Scand. 1969;75(2):313–322. [PubMed] [Google Scholar]
  16. Quarles J. M., Belding R. C., Beaman T. C., Gerhardt P. Hemodialysis culture of Serratia marcescens in a goat-artificial kidney-fermentor system. Infect Immun. 1974 Mar;9(3):550–558. doi: 10.1128/iai.9.3.550-558.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Reasoner D. J., Geldreich E. E. A new medium for the enumeration and subculture of bacteria from potable water. Appl Environ Microbiol. 1985 Jan;49(1):1–7. doi: 10.1128/aem.49.1.1-7.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Ridgway H. F., Olson B. H. Chlorine resistance patterns of bacteria from two drinking water distribution systems. Appl Environ Microbiol. 1982 Oct;44(4):972–987. doi: 10.1128/aem.44.4.972-987.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. du Moulin G. C. Airway colonization by Flavobacterium in an intensive care unit. J Clin Microbiol. 1979 Aug;10(2):155–160. doi: 10.1128/jcm.10.2.155-160.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. du Moulin G. C., Sherman I. H., Hoaglin D. C., Stottmeier K. D. Mycobacterium avium complex, an emerging pathogen in Massachusetts. J Clin Microbiol. 1985 Jul;22(1):9–12. doi: 10.1128/jcm.22.1.9-12.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]

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