PubMed · 4108170
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G N Rolinson, E J Russell. 1971-10-02. A new method for antibiotic sensitivity testing.. https://doi.org/10.1016/s0140-6736(71)92110-6
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Biofilms are formed by the aggregation of microorganisms into multicellular structures that adhere to surfaces. Here we show that bakers' yeast Saccharomyces cerevisiae can initiate biofilm formation. When grown in low-glucose medium, the yeast cells adhered avidly to a number of plastic surfaces. On semi-solid (0.3% agar) medium they formed "mats": complex multicellular structures composed of yeast-form cells. Both attachment to plastic and mat formation require Flo11p, a member of a large family of fungal cell surface glycoproteins involved in adherence. The ability to study biofilm formation in a tractable genetic system may facilitate the identification of new targets for antifungal therapy.
This study attempted to determine which combination of plaque or saliva, and tryptic soy agar, bacitracin (TSY20B) or mitis salivarius, bacitracin media, yielded the highest caries-predictive values for mutans counts in children with different caries prevalence. Sixty children were divided into three equally sized groups: caries free, low caries and high caries. Eighteen months later, their caries incidence and initial mutans count were compared. Fissure plaque on TSY20B yielded a high correlation between mutans counts and caries prevalence (P<0.009, r=3346) and incidence (P<0.003, r=4521). The caries-predictive values obtained demonstrate that the coefficient of variation of mutans counts from lower first-molar fissure plaque on TSY20B accounts for 20.4% of the variation in final caries index. This strong correlation provides a valuable tool for the identification of caries-prone individuals.
The methods currently available for the identification of the pathogenic yeast Candida dubliniensis all have disadvantages in that they are time-consuming, expensive, and/or, in some cases, unreliable. In a recent study (P. Staib and J. Morschhäuser, Mycoses 42:521-524; 1999) of 14 C. dubliniensis and 11 C. albicans isolates, it was suggested that the ability of C. dubliniensis to produce rough colonies and chlamydospores (chlamydoconidia) on Staib agar (SA) provided a simple means of differentiating it from its close relative C. albicans. In the present investigation, we examined the colony morphology and chlamydospore production of 130 C. dubliniensis and 166 C. albicans isolates on SA and on the related defined medium caffeic acid-ferric citrate agar (CAF). All of the C. dubliniensis and C. albicans isolates produced chlamydospores on the control medium, i.e., rice-agar-Tween agar. However, while none of the C. albicans isolates produced chlamydospores on either SA or CAF, 85.4 and 83.8% of the C. dubliniensis isolates produced chlamydospores on SA and CAF, respectively. All of the C. albicans isolates grew as smooth, shiny colonies on SA after 48 to 72 h of incubation at 30 degrees C, while 97.7% of the C. dubliniensis isolates grew as rough colonies, many (65%) with a hyphal fringe. In contrast, 87.4% of the C. albicans and 93.8% of the C. dubliniensis isolates yielded rough colonies on CAF. Although the results of this study confirm that SA is a good medium for distinguishing between C. dubliniensis and C. albicans, we believe that discrimination between these two species is best achieved on the basis of colony morphology rather than chlamydospore production.