Author:
Gade Lalitha,Scheel Christina M.,Pham Cau D.,Lindsley Mark D.,Iqbal Naureen,Cleveland Angela Ahlquist,Whitney Anne M.,Lockhart Shawn R.,Brandt Mary E.,Litvintseva Anastasia P.
Abstract
ABSTRACTExserohilum rostratumwas the major cause of an outbreak of fungal infections linked to injections of contaminated methylprednisolone acetate. Because almost 14,000 persons were exposed to product that was possibly contaminated with multiple fungal pathogens, there was unprecedented need for a rapid throughput diagnostic test that could detect bothE. rostratumand other unusual agents of fungal infection. Here we report development of a novel PCR test that allowed for rapid and specific detection of fungal DNA in cerebrospinal fluid (CSF), other body fluids and tissues of infected individuals. The test relied on direct purification of free-circulating fungal DNA from fluids and subsequent PCR amplification and sequencing. Using this method, we detectedExserohilum rostratumDNA in 123 samples from 114 case-patients (28% of 413 case-patients for whom 627 samples were available), andCladosporiumDNA in one sample from one case-patient. PCR with novelExserohilum-specific ITS-2 region primers detected 25 case-patients with samples that were negative using broad-range ITS primers. Compared to fungal culture, this molecular test was more sensitive: of 139 case-patients with an identical specimen tested by culture and PCR,E. rostratumwas recovered in culture from 19 (14%), but detected by PCR in 41 (29%), showing a diagnostic sensitivity of 29% for PCR compared to 14% for culture in this patient group. The ability to rapidly confirm the etiologic role ofE. rostratumin these infections provided an important contribution in the public health response to this outbreak.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
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