Use of FTA card for dry collection, transportation and storage of cervical cell specimen to detect high-risk HPV.

BACKGROUND The FTA elute micro card, which enable the collection, transport, and archiving of DNA could be an attractive alternative to a liquid based collection system for detection of human papillomavirus (HPV). OBJECTIVES To develop a method based on the FTA elute micro card for dry collection of cervical epithelial cell samples, suitable for subsequent PCR-based HPV testing. STUDY DESIGN The method was evaluated by a comparison of the DNA collected by cytobrush and the regular FTA elute micro card from 50 cervical cell samples. The method was then used to estimate the DNA amount in 1040 samples applied to the indicating FTA elute micro card. RESULT The agreement in HPV positivity between the cytobrush and FTA samples (94%) was excellent (kappa=0.88, 95% CI 0.748-1). All the 1040 samples on the indicating FTA card had sufficient amounts of genomic DNA (>10 copies of a single copy gene) to be suitable for HPV typing. In 53 of the 1040 women the day in the menstrual cycle was noted, and the copy number during follicular phase day 9-13 was found to be statistically significantly lower than for the other three stages in the menstrual cycle (day 4-8, 14, >14) and during menopause. CONCLUSION The indicating FTA elute micro card represents a suitable medium for collection of cervical cell samples, although follow-up studies are needed to verify the detection of low frequency HPV types.

[1]  S. Franceschi,et al.  Detection of cervical human papillomavirus infection in filter paper samples: a comparative study. , 2008, Journal of medical microbiology.

[2]  S Wacholder,et al.  HPV DNA testing in cervical cancer screening: results from women in a high-risk province of Costa Rica. , 2000, JAMA.

[3]  C. Hofacre,et al.  Molecular Detection and Serotyping of Infectious Bronchitis Virus from FTA® Filter Paper , 2005, Avian diseases.

[4]  C. Clavel,et al.  Human papillomavirus testing in primary screening for the detection of high-grade cervical lesions: a study of 7932 women , 2001, British Journal of Cancer.

[5]  S. Jameel,et al.  Direct detection of hepatitis B virus from dried blood spots by polymerase chain reaction amplification , 1992, Journal of clinical microbiology.

[6]  Lm Smith,et al.  Collecting, archiving and processing DNA from wildlife samples using FTA® databasing paper , 2004, BMC Ecology.

[7]  Julian Peto,et al.  Prevalence of Human Papillomavirus in Cervical Cancer: a Worldwide Perspective , 1995 .

[8]  J. L. Beebe,et al.  Evaluation of enzyme-linked immunoassay systems for detection of human immunodeficiency virus type 1 antibody from filter paper disks impregnated with whole blood , 1990, Journal of clinical microbiology.

[9]  R. Scott,et al.  Buccal DNA Collection: Comparison of Buccal Swabs with FTA Cards , 2006, Cancer Epidemiology Biomarkers & Prevention.

[10]  U. Gyllensten,et al.  High viral loads of human papillomavirus predict risk of invasive cervical carcinoma , 2005, British Journal of Cancer.

[11]  Michelle Thomas,et al.  Automated forensic DNA purification optimized for FTA card punches and identifiler STR-based PCR analysis. , 2007, Clinics in laboratory medicine.

[12]  J. Peto,et al.  Human papillomavirus is a necessary cause of invasive cervical cancer worldwide , 1999, The Journal of pathology.

[13]  U Menon,et al.  Management of women who test positive for high-risk types of human papillomavirus: the HART study , 2003, The Lancet.

[14]  U. Gyllensten,et al.  Real-Time PCR-Based System for Simultaneous Quantification of Human Papillomavirus Types Associated with High Risk of Cervical Cancer , 2003, Journal of Clinical Microbiology.

[15]  F. X. Bosch,et al.  Epidemiologic classification of human papillomavirus types associated with cervical cancer. , 2003, The New England journal of medicine.

[16]  Claude Fauquet,et al.  Classification of papillomaviruses. , 2004, Virology.

[17]  H. Guio,et al.  Method for efficient storage and transportation of sputum specimens for molecular testing of tuberculosis. , 2006, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

[18]  T. Iftner,et al.  Inclusion of HPV testing in routine cervical cancer screening for women above 29 years in Germany: results for 8466 patients , 2003, British Journal of Cancer.

[19]  J. Cuzick,et al.  HPV testing in primary screening of older women , 1999, British Journal of Cancer.

[20]  U. Gyllensten,et al.  Comparison between the Hybrid Capture 2 and the hpVIR real-time PCR for detection of human papillomavirus in women with ASCUS or low grade dysplasia. , 2009, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

[21]  M. García-Closas,et al.  Collection of buccal cell DNA using treated cards. , 2000, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[22]  B. Das,et al.  A simple 'paper smear' method for dry collection, transport and storage of cervical cytological specimens for rapid screening of HPV infection by PCR. , 2002, Journal of medical microbiology.