The enrichment feature of a selective serum-based transport medium for Campylobacter fetus was quantitatively examined. Preputial samples from artificial insemination bulls were spiked with known numbers of C fetus strains and inoculated into transport-enrichment medium (TEM). The survival and multiplication of these strains in TEM under different incubation periods and temperatures were assessed by plate counts. Mean enrichment values of 3.72 log and 4.42 log were observed after incubation at 37 degrees C for two and four days, respectively. There was no significant difference in the enrichment values between the C fetus subspecies venerealis strains and a C fetus subspecies fetus strain. Incubation of inoculated TEM vials at room temperature for up to two days neither improved the growth of C fetus nor affected its subsequent enrichment when the vials were reincubated at 37 degrees C. Comparison of the survival of C fetus with and without the use of TEM under simulated transport conditions demonstrated the superiority of TEM.

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http://dx.doi.org/10.1136/vr.115.17.434DOI Listing

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Article Synopsis
  • Isolation of Campylobacter fetus subsp. venerealis (Cfv) is critical for diagnosing bovine genital campylobacteriosis, which affects cattle fertility and poses a public health risk.
  • Current culture methods have low sensitivity, and there is no standard protocol for maximizing Cfv recovery, prompting this study to evaluate different transport, enrichment, and culture media.
  • The study found that using modified Lander's transport medium and storing samples for 24 hours at 21°C improved recovery rates, with Preston medium being the most effective for enrichment and microaerophilic conditions enhancing culture success.
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Objective: To determine clinical sensitivity and specificity of a quantitative real-time PCR (qRT-PCR) assay for Campylobacter fetus subsp venerealis (Cfv) in preputial samples of bulls.

Animals: 313 beef bulls.

Procedures: Preputial samples were collected from 300 virgin bulls and 13 Cfv-infected bulls.

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Objective: To compare the recovery rates of Campylobacter fetus subsp venerealis (Cfv) from preputial scrapings of infected bulls with passive filtration on selective medium versus nonselective medium, with and without transport medium.

Samples: 217 preputial scrapings from 12 bulls (4 naturally and 8 artificially infected with Cfv).

Procedures: Preputial scrapings were collected in 2 mL of PBS solution and bacteriologically cultured directly on Skirrow medium or passively filtered through 0.

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Validation of a monoclonal antibody-based capture enzyme-linked immunosorbent assay for detection of Campylobacter fetus.

Clin Diagn Lab Immunol

November 2005

Canadian Food Inspection Agency, Ottawa Laboratory Fallowfield, 3851 Fallowfield Rd., P.O. Box 11300 Stn. H, Ottawa, Ontario K2H 8P9, Canada.

A monoclonal antibody (MAb)-based antigen capture enzyme-linked immunosorbent assay (ELISA) was compared with the routine culture methodology for the detection of Campylobacter fetus subspecies from bovine and ovine field samples inoculated into Clark's transport enrichment medium (TEM). The work was a collaboration between two different diagnostic laboratories, one in Canada and the other in England. In both labs, TEM samples were incubated for 4 days at 35 degrees C and then tested by culture and ELISA.

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A monoclonal antibody-based enzyme-linked immunosorbent assay (ELISA) was described and evaluated for use as a presumptive screening test for detection of Campylobacter fetus in bovine preputial washing and vaginal mucus samples. A total of 725 diagnostic samples collected in the field and submitted in Clark's transport enrichment medium (TEM) were analyzed. Cultural isolation of C.

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