The production of filaments (germ tubes) by cells of Candida albicans in serum tubes permits presumptive identification to be made within two to three hours. The proportion of yeast-like cells forming filaments is progressively decreased with increasing cell concentration. The test is effective over a comparatively wide range of temperatures and using different types and concentrations of sera.

Journal Article↗

PubMed1934

The influence of vagal stimulation upon conduction through the branches of the a.-v. bundle in the dog.

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Journal Article↗

PubMedDate not supplied

Candidal infection of bone. Assessment of serologic tests in diagnosis and management.

In this case report, 30 sera from a 25-year-old heroin abuser with intervertebral candidosis were treated for the presence of anti-Candida albicans antibodies by agglutination, counterimmunoelectrophoresis, and indirect immunofluorescent assay. Sera were also adsorbed with heat-killed blastospores to remove antibodies against yeast-phase cells and tested by indirect immunofluorescent assay for anti-C. albicans germ tube antibodies (CAGTAs). Humoral responses to candidal 47-kD antigen were studied by immunoblotting in 23 unadsorbed sera. Anti-C. albicans antibodies were found in high titers by the three procedures but correlated poorly with the clinical evolution of the disease. CAGTAs were present from the beginning of the infection: Titers decreased in association with antifungal treatment and the patient's improvement, eventually becoming negative. Only class IgG antibodies to the 47-kD antigen were detected. These were present during the full course of the infection, failing to disappear at the end of the study. In this case, detection of CAGTAs appeared to be an important aid to diagnosis of the bony candidal infection, as they are detected early during the illness and seemed to have a prognostic significance.

Adult↗

PubMedDate not supplied

Monoclonal antibody-gold silver staining dot assay for the detection of antigenaemia in candidosis.

A monoclonal antibody (Mab), designated 5B2, reacting with cell wall mannoproteins of Candida albicans has been purified and coupled to colloidal gold. The ability of the gold conjugated Mab to detect C. albicans antigens in serum during infection has been assessed in a dot immunobinding assay involving an immunogold silver enhancement procedure (GSS). A double blind study was made with sera from 140 guinea pigs, including 40 control animals and 100 infected intravenously with C. albicans. Sera from infected animals were collected either 2 days (4 animals), 15 days (9 animals), or 21 days (87 animals) after inoculation. The overall sensitivity, specificity and positive predictive value of the test were 89, 95, and 98%, respectively. However, differences were encountered in the ratio of positive tests in relation to duration of the infection. Mab-GSS dot immunobinding has also been applied, together with Mab co-counterimmunoelectrophoresis on successive sera from 2 patients who recovered from clinically and mycologically proven episodes of systemic candidosis. It was demonstrated that both patients synthesized antibodies against glycoproteins sharing the 5B2 epitope, which was initially present transiently in their sera.

Animals↗