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Campylobacter fetus

Species of bacterium

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Through Gram-negative bacteria, Gastrointestinal disease and Vaccine

Morphology and identification

On cytology, C. fetus is a gram-negative rod, though may present coccoid under suboptimal conditions. A distinguishing feature of C. fetus is the "S-shape" of the rod, resembling thin, helical spirochaetes. C. fetus can be a highly motile organism by means of a single, unsheathed flagellum. Genus identification based on motility may be possible due to their characteristic corkscrew-like movement. C. fetus are non-spore forming and microaerophilic organisms that are both catalase and oxidase-positive, but non-fermentative.

Identification of C. fetus requires aseptic sample collection, followed by culture and potentially further biochemical and molecular methods. To increase the likelihood of successful growth, cultures on blood agar should be performed as soon as possible following collection. If samples are likely to be contaminated or faster growth is required, selective media or the use of antibiotics can be employed to inhibit growth of contaminants. Modified charcoal cefoperazone deoxycholate (CCD) agar is a growth medium designed to isolate Campylobacters from feces. On CCD agar, C. fetus will grow as grey colonies that may appear moist. Growth of C. fetus can be seen within 40–48 hours of incubation between 25–37 °C under microaerophilic conditions. Some, but not all species of C. fetus will grow at 42 °C. Because C. fetus is a fastidious organism to grow, positive cultures can be considered diagnostic, however negative cultures cannot rule out the possibility of infection.

Additional methods of identification may be used to diagnosis C. fetus to the subspecies level. Biochemical methods can identify subspecies of C. fetus, though may be considered unreliable. Campylobacter fetus subspecies fetus (Cff) can grow in 1% glycine and produce H2S, while C. fetus subspecies venerealis (Cfv) cannot. Growth of Cff will not occur in 3.5% NaCl. To increase reliability of identification, molecular methods such as polymerase chain reaction or DNA sequencing may be utilized. Other methods of identification include histology, immunohistochemistry, direct immunofluorescence, agglutination and enzyme-linked immunosorbent assay.

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