TY - JOUR KW - Humans KW - Adult KW - Female KW - Male KW - Middle Aged KW - High-Throughput Nucleotide Sequencing KW - Intraocular Lymphoma KW - Myeloid Differentiation Factor 88 KW - Cross-Sectional Studies KW - Aqueous Humor KW - Biomarkers, Tumor KW - DNA Mutational Analysis KW - DNA, Neoplasm KW - In Situ Hybridization KW - Lymphoma, B-Cell KW - Mutation AU - John Gonzales AU - Thuy Doan AU - Jessica Shantha AU - Michele Bloomer AU - Michael Wilson AU - Joseph DeRisi AU - Nisha Acharya AB -

INTRODUCTION: Currently, the detection of pathogens or mutations associated with intraocular lymphomas heavily relies on prespecified, directed PCRs. With metagenomic deep sequencing (MDS), an unbiased high-throughput sequencing approach, all pathogens as well as all mutations present in the host's genome can be detected in the same small amount of ocular fluid.

METHODS: In this cross-sectional case series, aqueous fluid samples from two patients were submitted to MDS to identify pathogens as well as common and rare cancer mutations.

RESULTS: MDS of aqueous fluid from the first patient with vitreal lymphoma revealed the presence of both Epstein-Barr virus (HHV-4/EBV) and human herpes virus 8 (HHV-8) RNA. Aqueous fluid from the second patient with intraocular B-cell lymphoma demonstrated a less common mutation in the gene associated with B-cell lymphoma.

CONCLUSION: MDS detects pathogens that, in some instances, may drive the development of intraocular lymphomas. Moreover, MDS is able to identify both common and rare mutations associated with lymphomas.

BT - Br J Ophthalmol DA - 2018 01 DO - 10.1136/bjophthalmol-2017-311151 IS - 1 J2 - Br J Ophthalmol LA - eng N2 -

INTRODUCTION: Currently, the detection of pathogens or mutations associated with intraocular lymphomas heavily relies on prespecified, directed PCRs. With metagenomic deep sequencing (MDS), an unbiased high-throughput sequencing approach, all pathogens as well as all mutations present in the host's genome can be detected in the same small amount of ocular fluid.

METHODS: In this cross-sectional case series, aqueous fluid samples from two patients were submitted to MDS to identify pathogens as well as common and rare cancer mutations.

RESULTS: MDS of aqueous fluid from the first patient with vitreal lymphoma revealed the presence of both Epstein-Barr virus (HHV-4/EBV) and human herpes virus 8 (HHV-8) RNA. Aqueous fluid from the second patient with intraocular B-cell lymphoma demonstrated a less common mutation in the gene associated with B-cell lymphoma.

CONCLUSION: MDS detects pathogens that, in some instances, may drive the development of intraocular lymphomas. Moreover, MDS is able to identify both common and rare mutations associated with lymphomas.

PY - 2018 SP - 6 EP - 8 T2 - Br J Ophthalmol TI - Metagenomic deep sequencing of aqueous fluid detects intraocular lymphomas. VL - 102 SN - 1468-2079 ER -