Literature DB >> 6784247

Detection of Salmonella C1, D and V1 antigens, by coagglutination, in blood cultures from patients with Salmonella infections.

R C Rockhill, M Lesmana, M A Moechtar, A Sutomo.   

Abstract

Protein A-containing Staphylococcus aureus was coupled to Salmonella C1, D and Vi monovalent antisera to produce C1-, D- and Vi-COAG reagents. The reagents were used to detect their homologous Salmonella antigens in blood cultures (BC). The D and Vi antigens were detected in 79 of 239 BC from patients with suspected typhoid fever and Salmonella typhi was later isolated from the same 79 BC. The C1 antigen was detected in 8 BC from which only S. oranienburg was later isolated. The COAG test was generally positive at the same time the BC became culture positive. However, because of subculture and biochemical identification requirements the COAG test could be interpreted 1-2 days before culture results were available. The COAG test can be used to presumptively identify Salmonella typhi and Salmonella group C1 in blood cultures before the culture results are available.

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Year:  1980        PMID: 6784247

Source DB:  PubMed          Journal:  Southeast Asian J Trop Med Public Health        ISSN: 0125-1562            Impact factor:   0.267


  4 in total

1.  Rapid diagnosis of typhoid fever.

Authors:  R Kalhan; I Kaur; R P Singh; H C Gupta
Journal:  Indian J Pediatr       Date:  1998 Jul-Aug       Impact factor: 1.967

2.  Rapid, economical diagnosis of enteric fever by a blood clot culture coagglutination procedure.

Authors:  I A Mikhail; W R Sanborn; J E Sippel
Journal:  J Clin Microbiol       Date:  1983-03       Impact factor: 5.948

3.  Detection of group D salmonellae in blood culture broth and of soluble antigen by tube agglutination using an O-9 monoclonal antibody latex conjugate.

Authors:  P L Lim; Y P Fok
Journal:  J Clin Microbiol       Date:  1987-07       Impact factor: 5.948

4.  Rapid diagnosis of typhoid fever through identification of Salmonella typhi within 18 hours of specimen acquisition by culture of the mononuclear cell-platelet fraction of blood.

Authors:  F A Rubin; P D McWhirter; D Burr; N H Punjabi; E Lane; S Kumala; P Sudarmono; S P Pulungsih; M Lesmana; P Tjaniadi
Journal:  J Clin Microbiol       Date:  1990-04       Impact factor: 5.948

  4 in total

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