This site needs JavaScript to work properly. Please enable it to take advantage of the complete set of features!
Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

NIH NLM Logo
Log in
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2015 Jun;240(6):742-51.
doi: 10.1177/1535370215583801. Epub 2015 Apr 22.

Laboratory diagnosis of melioidosis: past, present and future

Affiliations
Review

Laboratory diagnosis of melioidosis: past, present and future

Susanna K P Lau et al. Exp Biol Med (Maywood). 2015 Jun.

Abstract

Melioidosis is an emerging, potentially fatal disease caused by Burkholderia pseudomallei, which requires prolonged antibiotic treatment to prevent disease relapse. However, difficulties in laboratory diagnosis of melioidosis may delay treatment and affect disease outcomes. Isolation of B. pseudomallei from clinical specimens has been improved with the use of selective media. However, even with positive cultures, identification of B. pseudomallei can be difficult in clinical microbiology laboratories, especially in non-endemic areas where clinical suspicion is low. Commercial identification systems may fail to distinguish between B. pseudomallei and closely related species such as Burkholderia thailandensis. Genotypic identification of suspected isolates can be achieved by sequencing of gene targets such as groEL which offer higher discriminative power than 16S rRNA. Specific PCR-based identification of B. pseudomallei has also been developed using B. pseudomallei-specific gene targets such as Type III secretion system and Tat-domain protein. Matrix-assisted laser desorption ionization time-of-flight mass spectrometry, a revolutionary technique for pathogen identification, has been shown to be potentially useful for rapid identification of B. pseudomallei, although existing databases require optimization by adding reference spectra for B. pseudomallei. Despite these advances in bacterial identification, diagnostic problems encountered in culture-negative cases remain largely unresolved. Although various serological tests have been developed, they are generally unstandardized "in house" assays and have low sensitivities and specificities. Although specific PCR assays have been applied to direct clinical and environmental specimens, the sensitivities for diagnosis remain to be evaluated. Metabolomics is an uprising tool for studying infectious diseases and may offer a novel approach for exploring potential diagnostic biomarkers. The metabolomics profiles of B. pseudomallei culture supernatants can be potentially distinguished from those of related bacterial species including B. thailandensis . Further studies using bacterial cultures and direct patient samples are required to evaluate the potential of metabolomics for improving diagnosis of melioidosis.

Keywords: Burkholderia pseudomallei; Melioidosis; biomarkers; diagnosis; laboratory; metabolomics.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(a) PCA score plot and (b) PLS-DA score plot generated using MetaboAnalyst 3.0 (www.metaboanalyst.ca) in positive mode. Filtered culture supernatants were subject to UHPLC-ESI-Q-TOF-MS using Agilent 1290 UHPLC (Agilent Technologies, Santa Clara, CA USA). PLS-DA models were validated using R2 and Q2 based on leave one out cross-validation (LOOCV). Five-component model was selected as optimized model with R2= 1.00 and Q2 = 0.87. The significance of the model was demonstrated by permutation test with 2000 testing iterations using separation distance and P value < 0.001 was obtained. BC: B. cepacia complex; BPS: B. pseudomallei; BT: B. thailandensis; PA: P. aeruginosa; EC: E. coli. Three strains from each bacterial species were used for culture in RPMI 1640 medium ((#22400-089, Gibco, Carlsbad, CA, USA). (A color version of this figure is available in the online journal.)

References

    1. Kanaphun P, Thirawattanasuk N, Suputtamongkol Y, Naigowit P, Dance DA, Smith MD, White NJ. Serology and carriage of Pseudomonas pseudomallei: a prospective study in 1000 hospitalized children in northeast Thailand. J Infect Dis 1993; 167: 230–3. - PubMed
    1. Rattanavong S, Wuthiekanun V, Langla S, Amornchai P, Sirisouk J, Phetsouvanh R, Moore CE, Peacock SJ, Buisson Y, Newton PN. Randomized soil survey of the distribution of Burkholderia pseudomallei in rice fields in Laos. Appl Environ Microbiol 2011; 77: 532–6. - PMC - PubMed
    1. Prakash A, Thavaselvam D, Kumar A, Kumar A, Arora S, Tiwari S, Barua A, Sathyaseelan K. Isolation, identification and characterization of Burkholderia pseudomallei from soil of coastal region of India. Springerplus 2014; 3: 438. - PMC - PubMed
    1. Issack MI, Bundhun CD, Gokhool H. Melioidosis in Mauritius. Emerg Infect Dis 2005; 11: 139–40. - PMC - PubMed
    1. Inglis TJJ, Rolim DB, Sousa ADQ. Melioidosis in the Americas. Am J Trop Med Hyg 2006; 75: 947–54. - PubMed

Publication types

MeSH terms

Cite

AltStyle によって変換されたページ (->オリジナル) /