A novel cause of chronic viral meningoencephalitis: Cache Valley virus.
A novel cause of chronic viral meningoencephalitis: Cache Valley virus.
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DOI:
10.1002/ana.24982
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发表时间:
2017-07
影响因子:
11.2
通讯作者:
DeRisi JL
中科院分区:
文献类型:
--
作者:
Wilson MR;Suan D;Duggins A;Schubert RD;Khan LM;Sample HA;Zorn KC;Rodrigues Hoffman A;Blick A;Shingde M;DeRisi JL
Immunodeficient patients are particularly vulnerable to neuroinvasive infections that can be challenging to diagnose. Metagenomic next generation sequencing can identify unusual or novel microbes and is therefore well suited for investigating the etiology of chronic meningoencephalitis in immunodeficient patients. We present the case of a 34‐year‐old man with X‐linked agammaglobulinemia from Australia suffering from 3 years of meningoencephalitis that defied an etiologic diagnosis despite extensive conventional testing, including a brain biopsy. Metagenomic next generation sequencing of his cerebrospinal fluid and brain biopsy tissue was performed to identify a causative pathogen. Sequences aligning to multiple Cache Valley virus genes were identified via metagenomic next generation sequencing. Reverse transcription polymerase chain reaction and immunohistochemistry subsequently confirmed the presence of Cache Valley virus in the brain biopsy tissue. Cache Valley virus, a mosquito‐borne orthobunyavirus, has only been identified in 3 immunocompetent North American patients with acute neuroinvasive disease. The reported severity ranges from a self‐limiting meningitis to a rapidly fatal meningoencephalitis with multiorgan failure. The virus has never been known to cause a chronic systemic or neurologic infection in humans. Cache Valley virus has also never previously been detected on the Australian continent. Our research subject traveled to North and South Carolina and Michigan in the weeks prior to the onset of his illness. This report demonstrates that metagenomic next generation sequencing allows for unbiased pathogen identification, the early detection of emerging viruses as they spread to new locales, and the discovery of novel disease phenotypes. Ann Neurol 2017;82:105–114
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DOI:
10.1126/science.aaf5036
发表时间:
2016-04-15
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Faria NR;Azevedo RDSDS;Kraemer MUG;Souza R;Cunha MS;Hill SC;Thézé J;Bonsall MB;Bowden TA;Rissanen I;Rocco IM;Nogueira JS;Maeda AY;Vasami FGDS;Macedo FLL;Suzuki A;Rodrigues SG;Cruz ACR;Nunes BT;Medeiros DBA;Rodrigues DSG;Queiroz ALN;da Silva EVP;Henriques DF;da Rosa EST;de Oliveira CS;Martins LC;Vasconcelos HB;Casseb LMN;Simith DB;Messina JP;Abade L;Lourenço J;Alcantara LCJ;de Lima MM;Giovanetti M;Hay SI;de Oliveira RS;Lemos PDS;de Oliveira LF;de Lima CPS;da Silva SP;de Vasconcelos JM;Franco L;Cardoso JF;Vianez-Júnior JLDSG;Mir D;Bello G;Delatorre E;Khan K;Creatore M;Coelho GE;de Oliveira WK;Tesh R;Pybus OG;Nunes MRT;Vasconcelos PFC
通讯作者:
Vasconcelos PFC
影响因子:
48
作者:
Langmead, Ben;Salzberg, Steven L.
通讯作者:
Salzberg, Steven L.
影响因子:
3.7
作者:
Lee D;Das Gupta J;Gaughan C;Steffen I;Tang N;Luk KC;Qiu X;Urisman A;Fischer N;Molinaro R;Broz M;Schochetman G;Klein EA;Ganem D;Derisi JL;Simmons G;Hackett J Jr;Silverman RH;Chiu CY
通讯作者:
Chiu CY
DOI:
10.1093/bioinformatics/bts565
发表时间:
2012-12-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Fu L;Niu B;Zhu Z;Wu S;Li W
通讯作者:
Li W
影响因子:
2.1
作者:
Andreadis, Theodore G.;Armstrong, Philip M.;Main, Andrew J.
通讯作者:
Main, Andrew J.