Cargando…
Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens
BACKGROUND: Ocular infections remain a major cause of blindness and morbidity worldwide. While prognosis is dependent on the timing and accuracy of diagnosis, the etiology remains elusive in ~50 % of presumed infectious uveitis cases. The objective of this study is to determine if unbiased metagenom...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997733/ https://www.ncbi.nlm.nih.gov/pubmed/27562436 http://dx.doi.org/10.1186/s13073-016-0344-6 |
_version_ | 1782449832134180864 |
---|---|
author | Doan, Thuy Wilson, Michael R. Crawford, Emily D. Chow, Eric D. Khan, Lillian M. Knopp, Kristeene A. O’Donovan, Brian D. Xia, Dongxiang Hacker, Jill K. Stewart, Jay M. Gonzales, John A. Acharya, Nisha R. DeRisi, Joseph L. |
author_facet | Doan, Thuy Wilson, Michael R. Crawford, Emily D. Chow, Eric D. Khan, Lillian M. Knopp, Kristeene A. O’Donovan, Brian D. Xia, Dongxiang Hacker, Jill K. Stewart, Jay M. Gonzales, John A. Acharya, Nisha R. DeRisi, Joseph L. |
author_sort | Doan, Thuy |
collection | PubMed |
description | BACKGROUND: Ocular infections remain a major cause of blindness and morbidity worldwide. While prognosis is dependent on the timing and accuracy of diagnosis, the etiology remains elusive in ~50 % of presumed infectious uveitis cases. The objective of this study is to determine if unbiased metagenomic deep sequencing (MDS) can accurately detect pathogens in intraocular fluid samples of patients with uveitis. METHODS: This is a proof-of-concept study, in which intraocular fluid samples were obtained from five subjects with known diagnoses, and one subject with bilateral chronic uveitis without a known etiology. Samples were subjected to MDS, and results were compared with those from conventional diagnostic tests. Pathogens were identified using a rapid computational pipeline to analyze the non-host sequences obtained from MDS. RESULTS: Unbiased MDS of intraocular fluid produced results concordant with known diagnoses in subjects with (n = 4) and without (n = 1) uveitis. Samples positive for Cryptococcus neoformans, Toxoplasma gondii, and herpes simplex virus 1 as tested by a Clinical Laboratory Improvement Amendments-certified laboratory were correctly identified with MDS. Rubella virus was identified in one case of chronic bilateral idiopathic uveitis. The subject’s strain was most closely related to a German rubella virus strain isolated in 1992, one year before he developed a fever and rash while living in Germany. The pattern and the number of viral identified mutations present in the patient’s strain were consistent with long-term viral replication in the eye. CONCLUSIONS: MDS can identify fungi, parasites, and DNA and RNA viruses in minute volumes of intraocular fluid samples. The identification of chronic intraocular rubella virus infection highlights the eye’s role as a long-term pathogen reservoir, which has implications for virus eradication and emerging global epidemics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-016-0344-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4997733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49977332016-08-26 Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens Doan, Thuy Wilson, Michael R. Crawford, Emily D. Chow, Eric D. Khan, Lillian M. Knopp, Kristeene A. O’Donovan, Brian D. Xia, Dongxiang Hacker, Jill K. Stewart, Jay M. Gonzales, John A. Acharya, Nisha R. DeRisi, Joseph L. Genome Med Research BACKGROUND: Ocular infections remain a major cause of blindness and morbidity worldwide. While prognosis is dependent on the timing and accuracy of diagnosis, the etiology remains elusive in ~50 % of presumed infectious uveitis cases. The objective of this study is to determine if unbiased metagenomic deep sequencing (MDS) can accurately detect pathogens in intraocular fluid samples of patients with uveitis. METHODS: This is a proof-of-concept study, in which intraocular fluid samples were obtained from five subjects with known diagnoses, and one subject with bilateral chronic uveitis without a known etiology. Samples were subjected to MDS, and results were compared with those from conventional diagnostic tests. Pathogens were identified using a rapid computational pipeline to analyze the non-host sequences obtained from MDS. RESULTS: Unbiased MDS of intraocular fluid produced results concordant with known diagnoses in subjects with (n = 4) and without (n = 1) uveitis. Samples positive for Cryptococcus neoformans, Toxoplasma gondii, and herpes simplex virus 1 as tested by a Clinical Laboratory Improvement Amendments-certified laboratory were correctly identified with MDS. Rubella virus was identified in one case of chronic bilateral idiopathic uveitis. The subject’s strain was most closely related to a German rubella virus strain isolated in 1992, one year before he developed a fever and rash while living in Germany. The pattern and the number of viral identified mutations present in the patient’s strain were consistent with long-term viral replication in the eye. CONCLUSIONS: MDS can identify fungi, parasites, and DNA and RNA viruses in minute volumes of intraocular fluid samples. The identification of chronic intraocular rubella virus infection highlights the eye’s role as a long-term pathogen reservoir, which has implications for virus eradication and emerging global epidemics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-016-0344-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-25 /pmc/articles/PMC4997733/ /pubmed/27562436 http://dx.doi.org/10.1186/s13073-016-0344-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Doan, Thuy Wilson, Michael R. Crawford, Emily D. Chow, Eric D. Khan, Lillian M. Knopp, Kristeene A. O’Donovan, Brian D. Xia, Dongxiang Hacker, Jill K. Stewart, Jay M. Gonzales, John A. Acharya, Nisha R. DeRisi, Joseph L. Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title | Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title_full | Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title_fullStr | Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title_full_unstemmed | Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title_short | Illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
title_sort | illuminating uveitis: metagenomic deep sequencing identifies common and rare pathogens |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997733/ https://www.ncbi.nlm.nih.gov/pubmed/27562436 http://dx.doi.org/10.1186/s13073-016-0344-6 |
work_keys_str_mv | AT doanthuy illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT wilsonmichaelr illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT crawfordemilyd illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT chowericd illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT khanlillianm illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT knoppkristeenea illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT odonovanbriand illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT xiadongxiang illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT hackerjillk illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT stewartjaym illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT gonzalesjohna illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT acharyanishar illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens AT derisijosephl illuminatinguveitismetagenomicdeepsequencingidentifiescommonandrarepathogens |