1981
DOI: 10.1099/00222615-14-3-251
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Preparation of agglutinating antisera specific for the flagellar antigens of Pseudomonas aeruginosa

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Cited by 13 publications
(8 citation statements)
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“…Mares being mated after a difficult foaling are particularly vulnerable to infection (Hughes and Loy 1975), as is tissue damaged by a surgical procedure. The present study indicates that the most frequent P aeruginosa isolated was type 03, H3, which accounted for nearly 50 per cent of isolates, whereas Pitt (1981b) found an incidence of only 6.7 per cent in isolates from human cases. This may reflect a significant association of this serotype with infections in horses or, alternatively, its frequency of isolation may have been a consequence of the outbreaks.…”
Section: Discussioncontrasting
confidence: 43%
“…Mares being mated after a difficult foaling are particularly vulnerable to infection (Hughes and Loy 1975), as is tissue damaged by a surgical procedure. The present study indicates that the most frequent P aeruginosa isolated was type 03, H3, which accounted for nearly 50 per cent of isolates, whereas Pitt (1981b) found an incidence of only 6.7 per cent in isolates from human cases. This may reflect a significant association of this serotype with infections in horses or, alternatively, its frequency of isolation may have been a consequence of the outbreaks.…”
Section: Discussioncontrasting
confidence: 43%
“…A laboratory reference strain of P. aeruginosa (international antigenic typing scheme (IATS) serotype 0:1 (National Collection of Type Cultures 11440, American Type Culture Collection 3348), nonmucoid, piliated and gentamycin-sensitive) was used [16]. The bacteria were grown on blood agar plates for four consecutive days before overnight culture in tryptone soya broth (Unipath Ltd, Basingstoke, UK) to ensure piliation.…”
Section: Bacterial Strainmentioning
confidence: 99%
“…Methods for the preparation and characterisation of H-specific antisera, and the origin of the H-type strains, were described in the preceding paper (Pitt, 1981). 0 antisera.…”
Section: Serological Typing Methodsmentioning
confidence: 99%
“…Pooled H sera were not used in routine typing. Strains that were not H typable on first testing were passed twice through nitrate-containing soft agar in Craigie tubes (Pitt, 1981) and plated on agar. Cultures were re-tested by slide agglutination with the H-sera diluted to approximately one-tenth of the tray-test dilutions.…”
Section: Serological Typing Methodsmentioning
confidence: 99%