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Journal of Clinical Microbiology, July 2000, p. 2480-2483, Vol. 38, No. 7
Gamma-Dynacare Medical Laboratories,
Brampton,1 Choice in Health Clinic,
Toronto,2 and Regional Virology and
Chlamydiology Laboratory, St. Joseph's Hospital, McMaster University,
Hamilton,3 Ontario, Canada
Received 5 January 2000/Returned for modification 24 March
2000/Accepted 21 April 2000
Specimen pooling to achieve efficiency when testing urine specimens
for Chlamydia trachomatis nucleic acids has been suggested. We pooled endocervical swabs from 1,288 women and also tested individual swabs by ligase chain reaction (LCR). Out of 53 positive specimens, pools of 4 or 8 specimens missed two positives, providing 96.2% accuracy compared to individual test results. Dilution and positive-control spiking experiments showed that negative specimens with inhibitors of LCR in the pool reduced the signal. Conversely, two
extra positives, detected only through pooling, were negative by
individual testing but became positive after storage, suggesting that
fresh positive specimens with labile inhibitors may be positive in a
pool because of dilution of inhibitors. For this population of women
with a 4% prevalence of C. trachomatis infection,
substantial savings in cost of reagents (55 to 63%) and technologist
time (50 to 63%) made pooling strategies a desirable alternative to individual testing.
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Pooling Cervical Swabs and Testing by Ligase Chain Reaction Are
Accurate and Cost-Saving Strategies for Diagnosis of
Chlamydia trachomatis
*
Corresponding author. Mailing address: Gamma-Dynacare
Medical Laboratories, 115 Midair Court, Brampton, Ontario L6T 5M3,
Canada. Phone: (800) 668-2714 or (905) 790-3000. Fax: (905) 790-9331. E-mail: chernesk{at}fhs.mcmaster.ca.
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