2015
DOI: 10.1002/ana.24499
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Diagnosing Balamuthia mandrillarisEncephalitis With Metagenomic Deep Sequencing

Abstract: Objective Identification of a particular cause of meningoencephalitis can be challenging due to the myriad bacteria, viruses, fungi, and parasites that can produce overlapping clinical phenotypes, frequently delaying diagnosis and therapy. Metagenomic deep sequencing (MDS) approaches to infectious disease diagnostics are known for their ability to identify unusual or novel viruses and thus are well suited for investigating possible etiologies of meningoencephalitis. Methods We present the case of a 74 year-o… Show more

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Cited by 121 publications
(80 citation statements)
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References 24 publications
(61 reference statements)
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“…24,[46][47][48][49][50][51][52] Total RNA is extracted from a patient's CSF, and complementary DNA (cDNA) is generated by reverse transcription with random hexamer primers. The use of mNGS has gained momentum over the past several years, with several notable case reports and case series showcasing mNGS's ability to capture a broad range of infections with a single assay.…”
Section: Research Csf Metagenomic Sequencingmentioning
confidence: 99%
“…24,[46][47][48][49][50][51][52] Total RNA is extracted from a patient's CSF, and complementary DNA (cDNA) is generated by reverse transcription with random hexamer primers. The use of mNGS has gained momentum over the past several years, with several notable case reports and case series showcasing mNGS's ability to capture a broad range of infections with a single assay.…”
Section: Research Csf Metagenomic Sequencingmentioning
confidence: 99%
“…At this time, this testing is primarily being done only through research, but soon should be clinically available. 41 Several other infections to consider are shown in Table 7-4 and in the December 2015 issue of Continuum . 2 …”
Section: Consideration Of Rapidly Progressive Dementias By Etiologic mentioning
confidence: 99%
“…Double stranded complementary DNA next-generation sequencing libraries were generated and sequenced on an Illumina HiSeq 2500 machine (Illumina, San Diego, CA). [2] In total, 59,219,136 and paired-end 135 base pair (bp) sequences were obtained from the brain biopsy specimen, and 40,483,558 sequences were obtained from RNA extracted from the CSF. The sequences were processed through a rapid custom bioinformatics pipeline that involves quality filtering, iterative removal of sequences that align to the human genome and removal of low complexity and redundant sequences.…”
Section: Metagenomic Deep Sequencing Protocolmentioning
confidence: 99%
“…These remaining unique, complex and non-human sequences were classified to identify potential pathogens by comparing them to the entire National Center for Biotechnology Information's nucleotide reference database. [2] In both tissues, only common skin flora and reagent contaminants were identified.…”
Section: Metagenomic Deep Sequencing Protocolmentioning
confidence: 99%