Literature DB >> 10367639

Processing postmortem specimens with C18-carboxypropylbetaine and analysis by PCR to develop an antemortem test for Mycobacterium avium infections in ducks.

C G Thornton1, M R Cranfield, K M MacLellan, T L Brink, J D Strandberg, E A Carlin, J B Torrelles, J N Maslow, J L Hasson, D M Heyl, S J Sarro, D Chatterjee, S Passen.   

Abstract

Mycobacterium avium is the causative agent of the avian mycobacteriosis commonly known as avian tuberculosis (ATB). This infection causes disseminated disease, is difficult to diagnose, and is of serious concern because it causes significant mortality in birds. A new method was developed for processing specimens for an antemortem screening test for ATB. This novel method uses the zwitterionic detergent C18-carboxypropylbetaine (CB-18). Blood, bone marrow, bursa, and fecal specimens from 28 ducks and swabs of 20 lesions were processed with CB-18 for analysis by smear, culture, and polymerase chain reaction (PCR). Postmortem examination confirmed nine of these birds as either positive or highly suspect for disseminated disease. The sensitivities of smear, culture, and PCR, relative to postmortem analysis and independent of specimen type, were 44.4%, 88.9%, and 100%, respectively, and the specificities were 84.2%, 57.9%, and 15.8%, respectively. Reductions in specificity were due primarily to results among fecal specimens. However, these results were clustered among a subset of birds, suggesting that these tests actually identified birds in early stages of the disease. Restriction fragment length polymorphism mapping identified one strain of M. avium (serotype 1) that was isolated from lesions, bursa, bone marrow, blood, and feces of all but three of the culture-positive birds. In birds with confirmed disease, blood had the lowest sensitivity and the highest specificity by all diagnostic methods. Swabs of lesions provided the highest sensitivity by smear and culture (33.3% and 77.8%, respectively), whereas fecal specimens had the highest sensitivity by PCR (77.8%). The results of this study indicate that processing fecal specimens with CB-18, followed by PCR analysis, may provide a valuable first step for monitoring the presence of ATB in birds.

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Year:  1999        PMID: 10367639

Source DB:  PubMed          Journal:  J Zoo Wildl Med        ISSN: 1042-7260            Impact factor:   0.776


  4 in total

1.  Application of the C(18)-carboxypropylbetaine specimen processing method to recovery of Mycobacterium avium subsp. paratuberculosis from ruminant tissue specimens.

Authors:  Charles G Thornton; Kerry M MacLellan; Judith R Stabel; Christine Carothers; Robert H Whitlock; Selvin Passen
Journal:  J Clin Microbiol       Date:  2002-05       Impact factor: 5.948

2.  Comparison of the sodium dodecyl sulfate-sodium hydroxide specimen processing method with the C18-carboxypropylbetaine specimen processing method using the MB/BacT liquid culture system.

Authors:  J M Manterola; C G Thornton; E Padilla; J Lonca; I Corea; E Martínez; V Ausina
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2003-01-28       Impact factor: 3.267

3.  Comparison of C(18)-carboxypropylbetaine and standard N-acetyl-L-cysteine-NaOH processing of respiratory specimens for increasing tuberculosis smear sensitivity in Brazil.

Authors:  Cherise P Scott; Luciano Dos Anjos Filho; Fernanda Carvalho De Queiroz Mello; Charles G Thornton; William R Bishai; Leila S Fonseca; AfrAnio L Kritski; Richard E Chaisson; Yukari C Manabe
Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

4.  In vitro comparison of NALC-NaOH, tween 80, and C18-carboxypropylbetaine for processing of specimens for recovery of mycobacteria.

Authors:  C G Thornton; K M MacLellan; T L Brink; S Passen
Journal:  J Clin Microbiol       Date:  1998-12       Impact factor: 5.948

  4 in total

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