1996
DOI: 10.1128/cmr.9.3.405
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Identification methods for campylobacters, helicobacters, and related organisms

Abstract: The organisms which are referred to as campylobacteria are associated with a diverse range of diseases and habitats and are important from both clinical and economic perspectives. Accurate identification of these organisms is desirable for deciding upon appropriate therapeutic measures, and also for furthering our understanding of their pathology and epidemiology. However, the identification process is made difficult because of the complex and rapidly evolving taxonomy, fastidious nature, and biochemical inert… Show more

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Cited by 265 publications
(101 citation statements)
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References 171 publications
(308 reference statements)
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“…The inoculated petri dishes were incubated at 43°C for 48 h under microaerophilic conditions as described by Skirrow and Benjamin (1980) and colonies resembling Campylobacter were sub-cultured onto blood agar (Oxoid Ltd, Basingstoke, UK) at 43°C under micro-aerophilic conditions for 24 h. Suspected thermophilic Campylobacter colonies on blood agar that were Gramnegative, curved or spiral rods and showed corkscrew like motion, positive to catalase, oxidase and nitrate reduction tests were further tested for hippurate hydrolysis, H 2 S production and susceptibility to nalidixic acid and cephalothin. These parameters formed the basis for the identification of C. jejuni, C. coli or C. lari, as proposed by On (1996).…”
Section: Analysis Of Campylobactermentioning
confidence: 99%
“…The inoculated petri dishes were incubated at 43°C for 48 h under microaerophilic conditions as described by Skirrow and Benjamin (1980) and colonies resembling Campylobacter were sub-cultured onto blood agar (Oxoid Ltd, Basingstoke, UK) at 43°C under micro-aerophilic conditions for 24 h. Suspected thermophilic Campylobacter colonies on blood agar that were Gramnegative, curved or spiral rods and showed corkscrew like motion, positive to catalase, oxidase and nitrate reduction tests were further tested for hippurate hydrolysis, H 2 S production and susceptibility to nalidixic acid and cephalothin. These parameters formed the basis for the identification of C. jejuni, C. coli or C. lari, as proposed by On (1996).…”
Section: Analysis Of Campylobactermentioning
confidence: 99%
“…The growth of Campylobacter was detected by their characteristic appearance on culture media, i.e., the presence of flat grayish colonies resembling droplets of water sprayed on the medium. All suspected Campylobacter colonies on blood agar that were Gram-negative, curved, or spiral rods and showed corkscrew-like motion, positive to catalase, oxidase, and nitrate reduction tests were further tested for hippurate hydrolysis, H 2 S production, indoxyl acetate hydrolysis, urease production, and susceptibility to nalidixic acid and cephalothin (On 1996).…”
Section: Campylobacter Identificationmentioning
confidence: 99%
“…The inoculated Petri dishes were incubated at 42°C for 48 h under microaerophilic conditions and colonies resembling Campylobacter were sub-cultured onto blood agar (Oxoid Ltd, Basingstoke, UK) at 37°C under micro-aerophilic conditions for 24 h. Suspected thermophilic Campylobacter colonies on blood agar that were Gram negative, curved, or spiral rods and showed corkscrew-like motion; positive to catalase, oxidasem and nitrate reduction tests were further tested for hippurate hydrolysis, H 2 S production, and susceptibility to nalidixic acid and cephalothin. These parameters formed the basis for the identification of C. jejuni, C. coli, or Campylobacter lari as described by On (1996).…”
Section: Sample Collection and Handlingmentioning
confidence: 99%