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Calprotectin as a Biomarker for Melioidosis Disease Progression and Management
Author(s) -
Mohan Natesan,
Enoka Corea,
Shivankari Krishnananthasivam,
Harindra D. Sathkumara,
Jennifer L. Dankmeyer,
Beverly K. Dyas,
Kei Amemiya,
Aruna Dharshan De Silva,
Robert G. Ulrich
Publication year - 2017
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.02284-16
Subject(s) - melioidosis , calprotectin , burkholderia pseudomallei , biomarker , antibiotics , medicine , procalcitonin , c reactive protein , sepsis , immunology , gastroenterology , disease , inflammation , microbiology and biotechnology , biology , pathology , bacteria , biochemistry , inflammatory bowel disease , genetics
Melioidosis is a neglected tropical disease that is caused by the bacteriumBurkholderia pseudomallei and is underreported in many countries where the disease is endemic. A long and costly administration of antibiotics is needed to clear infections, and there is an unmet need for biomarkers to guide antibiotic treatment and increase the number of patients that complete therapy. We identified calprotectin as a lead biomarker ofB. pseudomallei infections and examined correlations between this serum protein and the antibiotic treatment outcomes of patients with melioidosis. Serum levels of calprotectin and C-reactive protein were significantly higher in patients with melioidosis and nonmelioidosis sepsis than in healthy controls. Median calprotectin levels were higher in patients with melioidosis than in those with nonmelioidosis sepsis, whereas C-reactive protein levels were similar in both groups. Notably, intensive intravenous antibiotic treatment of patients with melioidosis resulted in lower levels of calprotectin and C-reactive protein (P < 0.0001), coinciding with recovery. The median percent reduction of calprotectin and C-reactive protein was 71% for both biomarkers after antibacterial therapy. In contrast, we found no significant differences in calreticulin levels between the two melioidosis treatment phases. Thus, reductions in serum calprotectin levels were linked to therapeutic responses to antibiotics. Our results suggest that calprotectin may be a sensitive indicator of melioidosis disease activity and illustrate the potential utility of this biomarker in guiding the duration of antibiotic therapy.

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