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Clinical and Diagnostic Laboratory Immunology, March 1998, p. 219-224, Vol. 5, No. 2
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Blinded Multiplex PCR Analyses of Middle Ear and Nasopharyngeal Fluids from Chinchilla Models of Single- and Mixed-Pathogen-Induced Otitis Media

Lauren O. Bakaletz,1,* Gregory J. White,2 J. Christopher Post,2,3,4,5 and Garth D. Ehrlich2,3,4,5

Division of Otologic Research, Department of Otolaryngology, College of Medicine, The Ohio State University, Columbus, Ohio,1 and Departments of Pathology2 and Otolaryngology,3 University of Pittsburgh School of Medicine, Center for Genomic Sciences, University of Pittsburgh,4 and Department of Pediatric Otolaryngology, Children's Hospital of Pittsburgh,5 Pittsburgh, Pennsylvania

Received 29 May 1997/Returned for modification 18 July 1997/Accepted 11 December 1997

Multiplex PCR analyses for both bacterial and viral pathogens were conducted in a blinded manner on 33 archival specimens, of known culture status, procured from chinchilla models of both single- and mixed-pathogen-induced otitis media and from a pediatric patient. These specimens had been maintained at -70°C for up to 6 years. Experimental specimens evaluated included middle-ear effusions, nasopharyngeal lavage fluids and middle-ear lavage fluids from animals which were immunologically naive, sham-immunized or actively immunized with nontypeable Haemophilus influenzae antigens. Sampling times used ranged from the day of bacterial or viral challenge to 42 days after challenge. Initial PCR analyses of the 33 specimens matched the traditional culture data in 24 instances (73%), correctly identifying nontypeable H. influenzae, Moraxella catarrhalis, Streptococcus pneumoniae, or adenovirus as the causative agent. A PCR-positive signal for the microbe(s) inoculated was also obtained in four animal model specimens (12%) which were culture negative. One of two culture-negative human effusions was also PCR positive. Thus, overall, results obtained by blinded PCR were 85% concordant with traditional culture methods or correctly indicated the specific pathogen introduced in four specimens that were sterile. In no instance was a false-positive signal obtained for any of the five etiologic agents being evaluated. We conclude that the multiplex PCR analyses are rapid and accurate methodologies when they are used to retrospectively evaluate diverse archival specimens of limited volume from experimental models of otitis media.


* Corresponding author. Mailing address: Division of Otologic Research, Microbial Pathogenesis Section, The Ohio State University, Room 4331 UHC, 456 W. 10th Ave., Columbus, OH 43210-1282. Phone: (614) 293-8103. Fax: (614) 293-5506. E-mail: lbakalet{at}pop.service.ohio-state.edu.


Clinical and Diagnostic Laboratory Immunology, March 1998, p. 219-224, Vol. 5, No. 2
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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