6 research outputs found

    Clinical samples and laboratory results of primary and secondary BUD lesions.

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    <p><a href="http://www.plosntds.org/article/info:doi/10.1371/journal.pntd.0001747#pntd-0001747-t001" target="_blank">Table 1</a> shows samples collected from the primary and secondary lesions in July 2010 and 2011 and the corresponding laboratory results. “Neg” indicates a negative test result, “pos” indicates a positive test result.</p>a<p>MIC, microscopic examination of acid fast bacilli (AFB) following Ziehl-Neelsen staining conducted at CHR, DITM, and INH (samples from secondary lesion only).</p>b<p>IS<i>2404</i> PCR, conventional, single-step, gel-based IS<i>2404</i> polymerase-chain-reaction conducted at DITM.</p>c<p>IS<i>2404</i> qPCR, real-time quantitative IS<i>2404</i> polymerase-chain-reaction conducted at DITM.</p>d<p>16S RT qPCR, <i>Mycobacterium ulcerans</i>–specific reverse-transcription real-time quantitative polymerase-chain-reaction targeting the ribosomal 16S RNA of <i>M. ulcerans</i> conducted at DITM.</p>e<p>CUL, mycobacterial culture on Löwenstein-Jensen medium conducted at IML red, synlab, Asklepios Gauting, Germany.</p>f<p>FNA, fine-needle aspiration.</p>g<p>CLS, Puregene cell lysis solution, Qiagen, Germany.</p>h<p>ND, not done.</p>i<p>AFB, acid fast bacilli.</p>j<p>PANTA, transport medium for viable mycobacteria containing Polymyxin B, Amphotericin, Nalidixic acid, Trimethoprim, and Azlocillin.</p>k<p>No growth, culture result negative, no growth of acid fast bacilli.</p
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