1978
DOI: 10.1016/s0580-9517(08)70493-8
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Chapter VIII Serological Typing Methods of Leptospires

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Cited by 152 publications
(159 citation statements)
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“…Pathogens tested and specific methods of serologic testing for each of the agents evaluated have been described elsewhere (Table 1; Lindsey et al 1976;Dikken and Kmety 1978;Brown et al 1981;Dalton et al 1995;Plikaytis et al 1996;Nicholson et al 1997;Johnson et al 2000Johnson et al , 2005Martin et al 2000;Quinn et al 2002Quinn et al , 2004Dumler 2004;Semenova et al 2004;Jones et al 2007). Baseline seropositivity was interpreted as prior infection.…”
Section: Serological Testingmentioning
confidence: 99%
“…Pathogens tested and specific methods of serologic testing for each of the agents evaluated have been described elsewhere (Table 1; Lindsey et al 1976;Dikken and Kmety 1978;Brown et al 1981;Dalton et al 1995;Plikaytis et al 1996;Nicholson et al 1997;Johnson et al 2000Johnson et al , 2005Martin et al 2000;Quinn et al 2002Quinn et al , 2004Dumler 2004;Semenova et al 2004;Jones et al 2007). Baseline seropositivity was interpreted as prior infection.…”
Section: Serological Testingmentioning
confidence: 99%
“…MAT was performed following standard procedures (Wolff, 1954) using a panel of 36 group-specific rabbit antisera (group sera) representing all pathogenic serogroups. An isolate was considered to belong to the serogroup of the group serum that gave the highest titre (Dikken & Kmety, 1978).…”
Section: Serotypingmentioning
confidence: 99%
“…Each isolate was tested by MAT against all reference antisera of the identified serogroup to establish cross-reactivity patterns. CAAT was performed following a standard procedure (Dikken & Kmety, 1978) to identify the serovar status of the isolates. The Netherlands) to generate characteristic agglutination profiles, as described previously (Desmecht et al, 1991;Korver et al, 1988).…”
Section: Serotypingmentioning
confidence: 99%
“…Cross-agglutination absorption test (CAAT), the gold standard test for serological classification of Leptospira serovars, was repeatedly carried out by the Sokoine University of Agriculture (Tanzania) as described elsewhere (Stallman, 1987;Dikken & Kmety, 1978 Results from this study revealed that isolate RM1 is a pathogenic Leptospira as indicated by suppressed growth both at 13 uC and in the presence of 8-azaguanine. PCR with pathogenic primers Lepat 1 and Lepat 2 gave a DNA product of 330 bp ( Supplementary Fig.…”
mentioning
confidence: 99%