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Journal of Clinical Microbiology, April 2003, p. 1809, Vol. 41, No. 4
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.4.1809.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

LETTER TO THE EDITOR

Automated Identification Systems and Burkholderia pseudomallei


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LETTER
 
Lowe et al. (1) recently reported the failure of the Vitek 2 system (bioMérieux) to correctly identify Burkholderia pseudomallei. They also warned that thoughtless reliance on automation runs the risk that incorrectly identified organisms may be reported without question.

We recently had the opportunity to evaluate the new Phoenix (BD) automated identification and susceptibility testing system. Because melioidosis is an important infection in our region, we also tested strains of B. pseudomallei even though this organism is not in the Phoenix database.

Forty-seven nonduplicate strains of B. pseudomallei were used. The strains were all isolated from patients with compatible clinical histories. The strains were identified on the basis of their characteristic colony morphology on sheep blood agar and Ashdown's medium, bipolar staining of gram-negative rods, oxidase positivity, resistance to aminoglycosides and polymyxin B, and amino acid decarboxylase and dihydrolase reactions. All were identified by the API 20NE test (bioMérieux) as B. pseudomallei, except one that was identified as Chromobacterium violaceum. The 16S rRNA gene sequence of this isolate was identical to that of B. pseudomallei.

The NMIC/ID-4 card was used in accordance with the manufacturer's instructions. The results are shown in Table 1. The majority of B. pseudomallei strains were identified as Burkholderia cepacia. We were unable to discern a characteristic pattern of test results that would discriminate between the two species.


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  		TABLE 1. Identifications

Although B. pseudomallei is not in the Phoenix database, we felt it was important to evaluate how the system identified this organism, as the characteristic colony morphology may only become apparent after more than 24 h of incubation. It is therefore not improbable that an attempt may be made to identify an unknown strain by using the Phoenix system if B. pseudomallei is not suspected in the first place. Laboratories that use the BD Phoenix system should be aware that it will identify B. pseudomallei as B. cepacia with a high confidence value (95 to 99%).


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ACKNOWLEDGMENTS
 
The Phoenix and NMIC/ID-4 cards were kindly provided by BD.


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REFERENCE
 
    1
  1. Lowe, P., C. Engler, and R. Norton. 2002. Comparison of automated and nonautomated systems for identification of Burkholderia pseudomallei. J. Clin. Microbiol. 40:4625-4627.[Abstract/Free Full Text]
Tse Hsien Koh*
Lily Siew Yong Ng
Joanna Lee Foon Ho
Department of Laboratory Medicine
Changi General Hospital
2 Simei St. 3
529889 Singapore, Republic of Singapore

Li-Hwei Sng
Grace Chee Yeng Wang
Department of Pathology, Singapore General Hospital
169608 Singapore, Republic of Singapore

Raymond Valentine Tzer Pin Lin
Department of Laboratory Medicine
KK Women's and Children's Hospital
229899 Singapore, Republic of Singapore

* Phone: 65-68504962
Fax: 65-64269507
E-mail: gptthk{at}sgh.com.sg

Journal of Clinical Microbiology, April 2003, p. 1809, Vol. 41, No. 4
0095-1137/03/$08.00+0     DOI: 10.1128/JCM.41.4.1809.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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