The effect of oral bacteria on Candida albicans germ-tube formation

APMIS. 2001 Feb;109(2):147-54. doi: 10.1034/j.1600-0463.2001.d01-116.x.

Abstract

A total of eight bacterial isolates belonging to six species, and a select group of 12 oral Candida albicans isolates, were used to study the effect of bacteria on germ-tube formation. Briefly, each bacterial suspension (10(5-6) cells/ml) was mixed with a C. albicans suspension (10(7) cells/ml) and incubated at 37 degrees C for 90 min with bovine serum, and the percentage germ-tube-positive Candida cells was quantified using a haemocytometer, under light microscopy. In general, out of eight bacteria, Streptococcus sanguis SK21A, Streptococcus salivarius SK56, Escherichia coli ATCC 25922, and S. salivarius OBU3 suppressed germ-tube formation to varying degrees, with different C albicans isolates. Porphyromonas gingivalis Pg 50, Lactobacillus casei ATCC 7469 and Prevotella intermedia OBU4 elicited significant enhancement of germ-tube formation, whereas S. sanguis OBU 2 had no effect. E. coli ATCC 25922 was the only organism to show statistically significant suppression of germ-tube formation (p=0.0312). A significant increase in the germ tube production of C. albicans isolated from HIV-infected compared with HIV-free individuals was also noted. The current results tend to suggest that commensal and transient oral bacterial populations may selectively influence the differential expression of germ-tube-forming ability of C. albicans isolates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Candida albicans / growth & development*
  • Culture Media
  • Escherichia coli / physiology
  • Gram-Negative Bacteria / physiology*
  • Gram-Positive Bacteria / physiology*
  • HIV Infections / microbiology*
  • HIV-1*
  • Humans
  • Lacticaseibacillus casei / physiology
  • Mouth / microbiology*
  • Porphyromonas gingivalis / physiology
  • Prevotella intermedia / physiology
  • Streptococcus / physiology
  • Streptococcus sanguis / physiology

Substances

  • Culture Media