1970
DOI: 10.1128/aem.19.5.830-836.1970
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Application of Agglutinins for the Rapid and Accurate Identification of Medically Important Candida Species 1

Abstract: Agglutinins have been prepared against the medically important Candida species. Crude antisera to the various species demonstrated intense cross-reactions with heterologous yeastlike fungi as well as with many true yeasts. However, carefully monitored adsorptions of selected antisera allowed the production of six factor sera that proved useful in a slide agglutination test. These six sera permitted the rapid and specific identification of C. guilliermondii, C. krusei, C. parapsilosis, and C. pseudotropicalis. … Show more

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Cited by 26 publications
(6 citation statements)
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References 7 publications
(10 reference statements)
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“…Serotypes were determined with the Candida Check RM 302 Iatron Kit (Iatron Lab, Inc., Tokyo, Japan). Strains previously serotyped by standard procedures were employed as controls (29).…”
Section: Methodsmentioning
confidence: 99%
“…Serotypes were determined with the Candida Check RM 302 Iatron Kit (Iatron Lab, Inc., Tokyo, Japan). Strains previously serotyped by standard procedures were employed as controls (29).…”
Section: Methodsmentioning
confidence: 99%
“…Feet were measured with dial-type calipers (Schnelltaster, H. Krbplein GMBH, Schluechtern, Hesse, West Germany) before and after inoculation with antigen, and the net increase was determined. Antibodies were assayed by counterimmunoelectrophoresis (15,26) with a soluble cytoplasmic antigen (14) and by a whole-cell agglutination technique (34,36).…”
mentioning
confidence: 99%
“…A case of endocarditis was predicted to be caused by C. parapsilosis on the basis of an ID test on the patient's serum. Some 3 days later this prediction was confirmed by identifying the yeast species by the agglutination method of Sweet and Kaufman (12), and 3 weeks later it was confirmed by cultural methods. The unique precipitation band produced by C. parapsilosis has been described by Taschdjian et al (15).…”
Section: Discussionmentioning
confidence: 79%
“…Antigen preparation. Whole cell antigens were prepared from 48-hr dextrose-peptone-yeast extract broth cultures grown at 37 C by the method of Sweet and Kaufman (12). Working suspensions were prepared by diluting one part of packed cells in three parts of 0.5% formalinized saline and stored at 4 C. TMese antigens were used for (i) production of antisera, (ii) preparation of homogenates, and (iii) agglutination tests.…”
mentioning
confidence: 99%