<HashMap><database>MetaboLights</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/m_MTBLS14111_LC-MS_positive_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Tabular>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/m_MTBLS14111_LC-MS_negative_reverse-phase_metabolite_profiling_v2_maf.tsv</Tabular><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/s_MTBLS14111.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/i_Investigation.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/a_MTBLS14111_LC-MS_negative_reverse-phase_metabolite_profiling.txt</Txt><Txt>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111/a_MTBLS14111_LC-MS_positive_reverse-phase_metabolite_profiling.txt</Txt></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><ftp_download_link>ftp://ftp.ebi.ac.uk/pub/databases/metabolights/studies/public/MTBLS14111</ftp_download_link><metabolite_identification_protocol>&lt;p>Metabolite identification was performed by matching accurate mass-to-charge ratio (m/z), retention time, and MS/MS fragmentation spectra against public databases (HMDB, Metlin, MassBank, and GNPS) and a CSF-specific metabolite library, with a mass tolerance of ≤5 ppm and MS/MS similarity score ≥0.7. Isotopes and adducts were annotated using CAMERA or similar tools, and metabolites were classified based on their chemical class and biological function for downstream statistical analysis.&lt;/p></metabolite_identification_protocol><repository>MetaboLights</repository><study_status>Public</study_status><ptm_modification></ptm_modification><instrument_platform>Liquid Chromatography MS - negative - reverse-phase</instrument_platform><instrument_platform>Liquid Chromatography MS - positive - reverse-phase</instrument_platform><chromatography_protocol>&lt;p>Chromatographic separation was performed on an Agilent 1290 Infinity II UHPLC system equipped with an Agilent 1290 Infinity II autosampler, using two complementary columns: an ACQUITY UPLC BEH C18 reverse-phase column (both 2.1 × 150 mm, 1.7 μm), each protected by a matching guard column. The column temperature was maintained at 45 °C, with mobile phases composed of acetonitrile, water, ammonium acetate, and formic acid, optimized for broad-spectrum metabolite detection in cerebrospinal fluid.&lt;/p></chromatography_protocol><publication>Characterization Epstein-Barr Virus-Associated Encephalitis via Identification of Metabolomic Biomarkers.</publication><submitter_affiliation>Southern medical University</submitter_affiliation><submitter_name>Muzi Wen</submitter_name><organism_part>Cerebrospinal fluid</organism_part><organism_part>Pooled sample</organism_part><technology_type>mass spectrometry assay</technology_type><disease></disease><extraction_protocol>&lt;p>Frozen CSF samples were thawed on ice and centrifuged at 10,000 g for 10 min at 4 °C to remove cellular debris. A 200 μL aliquot of supernatant was mixed with 800 μL of pre-cooled methanol (containing internal standards) to precipitate proteins, followed by vortexing and centrifugation at 12,000 g for 15 min at 4 °C. The supernatant was dried under vacuum, reconstituted in 100 μL of acetonitrile-water (9:1, v/v), and filtered through a 0.22 μm membrane before LC-MS analysis.&lt;/p></extraction_protocol><organism>Homo sapiens</organism><full_dataset_link>https://www.ebi.ac.uk/metabolights/MTBLS14111</full_dataset_link><author>Wenbin Pan.</author><author>Suyue Pan.</author><author>Gaoling Li.</author><author>Muzi Wen. Nanfang Hospital. Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou Road North 8838#, Guangzhou, China, 510515, China. Muzikk0080@163.com.</author><author>Chao Yuan.</author><author>Pei Shang. Nanfang Hospital. andy.shang666@hotmail.com.</author><author>Yuqiao Liao. Nanfang Hospital. cristy_lyq@163.com.</author><author>Ruoyi Zheng. Nanfang Hospital. Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou Road North 8838#, Guangzhou, China, 510515, China;. ZhengCindy324@163.com.</author><data_transformation_protocol>&lt;p>Raw LC-MS data were imported into commercial metabolomics software (e.g., Compound Discoverer 3.3, MS-DIAL, or XCMS Online) for peak detection, alignment, noise filtering, and normalization. Internal standards were used for quality control and signal correction, and only features with consistent detection across QC samples were retained for further analysis.&lt;/p></data_transformation_protocol><study_factor>Treatment</study_factor><submitter_email>Muzikk0080@163.com</submitter_email><sample_collection_protocol>&lt;p>Organism: Homo sapiens (Human)&lt;/p>&lt;p>Sample type: Cerebrospinal fluid (CSF)&lt;/p>&lt;p>Treatment groups: Antiviral drugs treatment; No treatment (control)&lt;/p>&lt;p>Collection method: CSF samples were collected via lumbar puncture at the L4–L5 intervertebral space using a 22G spinal needle. Approximately 10 mL of CSF was collected from each subject and immediately stored at −80 °C until analysis.&lt;/p>&lt;p>&amp;nbsp;&lt;/p></sample_collection_protocol><omics_type>Metabolomics</omics_type><study_design>Metabolomics</study_design><study_design>Acute disseminated encephalomyelitis</study_design><study_design>Epstein-Barr Virus</study_design><study_design>encephalitis</study_design><study_design>cerebrospinal fluid</study_design><curator_keywords>Metabolomics</curator_keywords><curator_keywords>Acute disseminated encephalomyelitis</curator_keywords><curator_keywords>Epstein-Barr Virus</curator_keywords><curator_keywords>encephalitis</curator_keywords><curator_keywords>cerebrospinal fluid</curator_keywords><mass_spectrometry_protocol>&lt;p>Mass spectrometric detection was carried out using a Q Exactive HF-X Orbitrap mass spectrometer (Thermo Fisher Scientific) coupled to the UHPLC system, equipped with a Heated Electrospray Ionization (HESI-II) source operating in both positive and negative ion modes. The quadrupole-Orbitrap hybrid mass analyzer was set to scan over an m/z range of 70–1050 for full MS acquisition and 50–1050 for data-dependent MS/MS acquisition, enabling high-resolution accurate mass measurement and comprehensive metabolite fragmentation analysis.&lt;/p></mass_spectrometry_protocol><metabolite_name>(+/-)-Equol</metabolite_name><metabolite_name>Prostaglandin G2</metabolite_name><metabolite_name>Lipoxin B4</metabolite_name><metabolite_name>6Ï«-Prostaglandin I1</metabolite_name><metabolite_name>Phenylacetylglutamine</metabolite_name><metabolite_name>(2R)-2,3-Dihydroxypropanoic acid</metabolite_name><metabolite_name>Folic acid</metabolite_name><metabolite_name>13(S)-HOTrE</metabolite_name><metabolite_name>N-Acetyl-L-histidine</metabolite_name><metabolite_name>4-(anilinomethylidene)-3-methyl-4,5-dihydroisoxazol-5-one</metabolite_name><metabolite_name>Deoxyinosine</metabolite_name><metabolite_name>Cytidine-5'-monophosphate</metabolite_name><metabolite_name>Dl-3,4-Dihydroxymandelic Acid</metabolite_name><metabolite_name>D-(-)-Mannitol</metabolite_name><metabolite_name>N-Acetylvaline</metabolite_name><metabolite_name>Isobutyryl carnitine</metabolite_name><metabolite_name>Hexanoylglycine</metabolite_name><metabolite_name>(+/-)5(6)-DiHET</metabolite_name><metabolite_name>3,8,9-trihydroxy-10-propyl-3,4,5,8,9,10-hexahydro-2H-oxecin-2-one</metabolite_name><metabolite_name>Quercetin-3ÉÇ-D-glucoside</metabolite_name><metabolite_name>Prostaglandin H2</metabolite_name><metabolite_name>Phenylglyoxylic acid</metabolite_name><metabolite_name>N2-Methylguanosine</metabolite_name><metabolite_name>FAHFA 18:2/20:4</metabolite_name><metabolite_name>Capric acid</metabolite_name><metabolite_name>1-Methylxanthine</metabolite_name><metabolite_name>D-Glucuronic acid</metabolite_name><metabolite_name>Syringic acid</metabolite_name><metabolite_name>2-Methylbutyroylcarnitine</metabolite_name><metabolite_name>13,14-dihydro-15-keto Prostaglandin D1</metabolite_name><metabolite_name>Ursolic acid</metabolite_name><metabolite_name>Capryloylglycine</metabolite_name><metabolite_name>Neopterin</metabolite_name><metabolite_name>6-(Dimethylamino)purine</metabolite_name><metabolite_name>PG 16:0_18:1</metabolite_name><metabolite_name>17Ï«-Hydroxyprogesterone</metabolite_name><metabolite_name>Dl-Indole-3-lactic acid</metabolite_name><metabolite_name>Prostaglandin E2</metabolite_name><metabolite_name>Prostaglandin E1</metabolite_name><metabolite_name>Prostaglandin E3</metabolite_name><metabolite_name>trans-10-Heptadecenoic Acid</metabolite_name><metabolite_name>Agnuside</metabolite_name><metabolite_name>20-Carboxy-Leukotriene B4</metabolite_name><metabolite_name>Mevalonic acid</metabolite_name><metabolite_name>Pyridoxamine 5-phosphate</metabolite_name><metabolite_name>Aflatoxin G1</metabolite_name><metabolite_name>Methyltestosterone</metabolite_name><metabolite_name>(2E)-4-Hydroxy-3,7-dimethyl-2,6-octadien-1-yl beta-D-glucopyranoside</metabolite_name><metabolite_name>PE 18:0_22:6</metabolite_name><metabolite_name>PE 18:0_22:5</metabolite_name><metabolite_name>D-(+)-Maltose</metabolite_name><metabolite_name>(+/-)12(13)-DiHOME</metabolite_name><metabolite_name>Glycitein</metabolite_name><metabolite_name>Pseudouridine</metabolite_name><metabolite_name>Isophorone</metabolite_name><metabolite_name>N-Acetylneuraminic acid</metabolite_name><metabolite_name>4-Pyridoxic acid</metabolite_name><metabolite_name>Pantothenic acid</metabolite_name><metabolite_name>10-Undecenoic acid</metabolite_name><metabolite_name>glutathione disulfide</metabolite_name><metabolite_name>3-[4-(tert-butyl)anilino]-2-(3-thienylcarbonyl)acrylonitrile</metabolite_name><metabolite_name>Isovaleric acid</metabolite_name><metabolite_name>Guanosine</metabolite_name><metabolite_name>N-Acetyl-L-methionine</metabolite_name><metabolite_name>3-Hydroxydecanoic acid</metabolite_name><metabolite_name>12(S)-HETE</metabolite_name><metabolite_name>4-Acetamidobutyric Acid</metabolite_name><metabolite_name>D-Glucosamine 6-phosphate</metabolite_name><metabolite_name>5'-S-Methyl-5'-thioadenosine</metabolite_name><metabolite_name>Chenodeoxycholic Acid</metabolite_name><metabolite_name>dUDP</metabolite_name><metabolite_name>Spiculisporic Acid</metabolite_name><metabolite_name>Guanosine triphosphate (GTP)</metabolite_name><metabolite_name>Triacanthine</metabolite_name><metabolite_name>L-Anserine</metabolite_name><metabolite_name>LPE 22:6</metabolite_name><metabolite_name>N-{[2-(2-thienyl)-1,3-thiazol-4-yl]methyl}benzamide</metabolite_name><metabolite_name>Hexadecanedioic acid</metabolite_name><metabolite_name>Oxaceprol</metabolite_name><metabolite_name>PC 18:0_22:4</metabolite_name><metabolite_name>3-Furoic acid</metabolite_name><metabolite_name>3-Coumaric acid</metabolite_name><metabolite_name>3-{[(4-amino-1,3,5-triazin-2-yl)thio]methyl}benzonitrile</metabolite_name><metabolite_name>Prostaglandin D3</metabolite_name><metabolite_name>1-(4-methylphenyl)-3-(2-pyridylthio)pyrrolidine-2,5-dione</metabolite_name><metabolite_name>Isorhamnetin</metabolite_name><metabolite_name>Asp-glu</metabolite_name><metabolite_name>Naringin</metabolite_name><metabolite_name>8Z,11Z,14Z-Eicosatrienoic acid</metabolite_name><metabolite_name>LPE 8:0</metabolite_name><metabolite_name>Uridine</metabolite_name><metabolite_name>Asaraldehyde</metabolite_name><metabolite_name>D-Gluconic acid</metabolite_name><metabolite_name>N-Acetyl-DL-tryptophan</metabolite_name><metabolite_name>5-Aminosalicylic Acid</metabolite_name><metabolite_name>trans-Petroselinic acid</metabolite_name><metabolite_name>Homogentisic Acid</metabolite_name><metabolite_name>Vitamin B2</metabolite_name><metabolite_name>LPC 20:3</metabolite_name><metabolite_name>LPC 20:4</metabolite_name><metabolite_name>Androsterone glucuronide</metabolite_name><metabolite_name>Equol</metabolite_name><metabolite_name>Dulcitol</metabolite_name><metabolite_name>Prostaglandin A2</metabolite_name><metabolite_name>Prostaglandin A3</metabolite_name><metabolite_name>Testosterone sulfate</metabolite_name><metabolite_name>Orotidine 5'-monophosphate</metabolite_name><metabolite_name>DL-3,4-Dihydroxyphenyl glycol</metabolite_name><metabolite_name>PE 18:1_22:6</metabolite_name><metabolite_name>3-benzyl-1-butyl-4-hydroxy-1,2-dihydroquinolin-2-one</metabolite_name><metabolite_name>beta-Nicotinamide mononucleotide</metabolite_name><metabolite_name>Glycoursodeoxycholic acid</metabolite_name><metabolite_name>Lysope 18:1</metabolite_name><metabolite_name>2-[(4-chlorophenyl)sulfonyl]-N,N-dimethylacetamide</metabolite_name><metabolite_name>2-Hydroxyestradiol</metabolite_name><metabolite_name>Uric acid</metabolite_name><metabolite_name>Prostaglandin B2</metabolite_name><metabolite_name>ÉÇ-Estradiol</metabolite_name><metabolite_name>L-(+)-Tartaric acid</metabolite_name><metabolite_name>3-Hydroxy-3-methylglutaric acid</metabolite_name><metabolite_name>23-Norcholic acid</metabolite_name><metabolite_name>L-Tyrosine</metabolite_name><metabolite_name>Adipamide</metabolite_name><metabolite_name>1,5-Anhydro-D-glucitol</metabolite_name><metabolite_name>Cyclohexaneacetic acid</metabolite_name><metabolite_name>3-Hydroxybutyric acid</metabolite_name><metabolite_name>2-Isopropylmalate</metabolite_name><metabolite_name>Phenylpyruvic acid</metabolite_name><metabolite_name>2-Deoxyuridine</metabolite_name><metabolite_name>GTP</metabolite_name><metabolite_name>Melatonin</metabolite_name><metabolite_name>Ascorbic acid</metabolite_name><metabolite_name>Sucrose</metabolite_name><metabolite_name>2-Methylbutyl beta-D-glucopyranoside</metabolite_name><metabolite_name>2-Hydroxy-2-methyl-3-buten-1-yl beta-D-glucopyranoside</metabolite_name><metabolite_name>Tetradecanedioic acid</metabolite_name><metabolite_name>Propionyl-L-carnitine</metabolite_name><metabolite_name>Docosahexaenoic acid</metabolite_name><metabolite_name>gamma-Glutamyltyrosine</metabolite_name><metabolite_name>Sedoheptulose 1,7-bisphosphate</metabolite_name><metabolite_name>LPE 20:4</metabolite_name><metabolite_name>LPE O-18:1</metabolite_name><metabolite_name>PC(16:0/16:0)</metabolite_name><metabolite_name>PE O-17:1_22:6</metabolite_name><metabolite_name>Phloretin</metabolite_name><metabolite_name>LPC 18:2</metabolite_name><metabolite_name>Thromoboxane B1</metabolite_name><metabolite_name>N-Acetyl-L-tyrosine</metabolite_name><metabolite_name>Taurocholic acid</metabolite_name><metabolite_name>gamma-Glutamylleucine</metabolite_name><metabolite_name>gamma-Glutamylmethionine</metabolite_name><metabolite_name>LPC 18:0</metabolite_name><metabolite_name>LPC 18:1</metabolite_name><metabolite_name>PC O-16:0_22:6</metabolite_name><metabolite_name>11ÉÇ-Prostaglandin E2</metabolite_name><metabolite_name>4-benzyl-N-(3,5-dichlorophenyl)-1,4-diazepane-1-carboxamide</metabolite_name><metabolite_name>PE O-18:0_22:4</metabolite_name><metabolite_name>Glutamic acid</metabolite_name><metabolite_name>Suberic acid</metabolite_name><metabolite_name>15(R),19(R)-Hydroxy prostaglandin F2Ï«</metabolite_name><metabolite_name>5-Methylcytidine</metabolite_name><metabolite_name>L-Threonic acid</metabolite_name><metabolite_name>Rifampicin</metabolite_name><metabolite_name>N-Acetyl-aspartic acid</metabolite_name><metabolite_name>D-Pantethine</metabolite_name><metabolite_name>N-Sulfo-glucosamine sodium salt</metabolite_name><metabolite_name>D-Threose</metabolite_name><metabolite_name>Citric acid</metabolite_name><metabolite_name>L-serine</metabolite_name><metabolite_name>Prostaglandin F3Ï«</metabolite_name><metabolite_name>(3beta,9xi)-3-(beta-D-Glucopyranosyloxy)-14-hydroxycard-20(22)-enolide</metabolite_name><metabolite_name>2-Arachidonyl glycerol ether</metabolite_name><metabolite_name>P-Toluenesulfonic acid</metabolite_name><metabolite_name>Prostaglandin K2</metabolite_name><metabolite_name>11-Epiprostaglandin E1</metabolite_name><metabolite_name>15(R),19(R)-Hydroxy prostaglandin F1Ï«</metabolite_name><metabolite_name>Glycocholic acid</metabolite_name><metabolite_name>Adenosine 3'5'-cyclic monophosphate</metabolite_name><metabolite_name>P-Coumaroyl Agmatine</metabolite_name><metabolite_name>Levodopa</metabolite_name><metabolite_name>5-Aminopentanoate</metabolite_name><metabolite_name>Jasmonic acid</metabolite_name><metabolite_name>L-Ascorbate</metabolite_name><metabolite_name>Tretinoin</metabolite_name><metabolite_name>2-Hydroxycaproic acid</metabolite_name><metabolite_name>3-Phenyllactic acid</metabolite_name><metabolite_name>Milbemectin A4</metabolite_name><metabolite_name>11-Ketoetiocholanolone</metabolite_name><metabolite_name>Adrenosterone</metabolite_name><metabolite_name>D-(+)-Galactose</metabolite_name><metabolite_name>Acetaminophen glucuronide</metabolite_name><metabolite_name>Indole-3-lactic acid</metabolite_name><metabolite_name>2-(4-aminophenoxy)isophthalonitrile</metabolite_name><metabolite_name>Ofloxacin impurity E</metabolite_name><metabolite_name>Monobutyl phthalate</metabolite_name><metabolite_name>Taurochenodeoxycholic acid</metabolite_name><metabolite_name>PE O-18:0_20:4</metabolite_name><metabolite_name>2-Aminoadipic acid</metabolite_name><metabolite_name>Vanillyl alcohol</metabolite_name><metabolite_name>Adenosine 5'-phosphosulfate</metabolite_name><metabolite_name>23-Nordeoxycholic acid</metabolite_name><metabolite_name>Genistein</metabolite_name><metabolite_name>PG 18:0_18:1</metabolite_name><metabolite_name>Hydrocortisone</metabolite_name><metabolite_name>N-Acetyl-Dl-glutamic acid</metabolite_name><metabolite_name>10-Hydroxydecanoic acid</metabolite_name><metabolite_name>Ethyl-ÉÇ-D-glucuronide</metabolite_name><metabolite_name>cis-Aconitic acid</metabolite_name><metabolite_name>4-Hydroxy-3- methoxyphenylglycol sulfate</metabolite_name><metabolite_name>7-Ketolithocholic acid</metabolite_name><metabolite_name>D(-)-Amygdalin</metabolite_name><metabolite_name>Glycochenodeoxycholic acid</metabolite_name><metabolite_name>1-Methyluric acid</metabolite_name><metabolite_name>(©I)9-HpODE</metabolite_name><metabolite_name>N-Acetylalanine</metabolite_name><metabolite_name>Punicic Acid</metabolite_name><metabolite_name>CTP</metabolite_name><metabolite_name>Taurine</metabolite_name><metabolite_name>L-Cysteine-glutathione gisulfide</metabolite_name><metabolite_name>Gamma-Glu-Leu</metabolite_name><metabolite_name>DL-4-Hydroxyphenyllactic acid</metabolite_name><metabolite_name>Ñ´-Ribono-1,4-lactone</metabolite_name><metabolite_name>Lithocholic acid</metabolite_name><metabolite_name>MAG (18:2)</metabolite_name><metabolite_name>FAHFA 16:0/18:2</metabolite_name><metabolite_name>2-Hydroxyhippuric acid</metabolite_name><metabolite_name>N-Acetylsphingosine</metabolite_name><metabolite_name>PE O-16:1_22:6</metabolite_name><metabolite_name>Tetrahydroaldosterone</metabolite_name><metabolite_name>o-Toluic Acid</metabolite_name><metabolite_name>5-Hydroxytryptophan</metabolite_name><metabolite_name>2-[(3S)-1-(Cyclohexylmethyl)-3-pyrrolidinyl]-5-fluoro-1H-benzimidazole</metabolite_name><metabolite_name>4-Hydroxybenzylcyanide</metabolite_name><metabolite_name>alpha-Ketoglutaric acid</metabolite_name><metabolite_name>Ï«-Aspartylphenylalanine</metabolite_name><metabolite_name>LPC 14:0</metabolite_name><metabolite_name>ST 24:2;O4</metabolite_name><metabolite_name>Methyl 3-indolyacetate</metabolite_name><metabolite_name>N-Acetyl-Asp-Glu</metabolite_name><metabolite_name>N-lactoyl-phenylalanine</metabolite_name><metabolite_name>Porphobilinogen</metabolite_name><metabolite_name>All-cis-4,7,10,13,16-docosapentaenoic acid</metabolite_name><metabolite_name>MAG (18:3)</metabolite_name><metabolite_name>4-Oxoproline</metabolite_name><metabolite_name>L-Arabinitol</metabolite_name><metabolite_name>Ibuprofen metabolite B</metabolite_name><metabolite_name>N6-Succinyl Adenosine</metabolite_name><metabolite_name>Chlortetracycline</metabolite_name><metabolite_name>PE-Cer 12:1;2O/22:0</metabolite_name><metabolite_name>Lauric acid</metabolite_name><metabolite_name>Calcitriol</metabolite_name><metabolite_name>6-bromo-3-(2-phenylethanhydrazonoyl)-2H-chromen-2-one</metabolite_name><metabolite_name>6-Deoxy-D-glucose</metabolite_name><metabolite_name>3,5-dimethyl-N'-[4-(trifluoromethyl)benzoyl]isoxazole-4-carbohydrazide</metabolite_name><metabolite_name>L-Tryptophan</metabolite_name><metabolite_name>4-Butylresorcinol</metabolite_name><metabolite_name>Pentadecanoic acid</metabolite_name><metabolite_name>N'-(4-methoxybenzoyl)-2-[(1-naphthylmethyl)thio]acetohydrazide</metabolite_name><metabolite_name>LPC 15:0</metabolite_name><metabolite_name>13,14-Dihydro-15-keto Prostaglandin A2</metabolite_name><metabolite_name>Serotonin</metabolite_name><metabolite_name>FAHFA 18:0/20:2</metabolite_name><metabolite_name>Ferulic acid</metabolite_name><metabolite_name>8,15-Dihete</metabolite_name><metabolite_name>2-Methoxyestradiol</metabolite_name><metabolite_name>2-(Formylamino)Benzoic Acid</metabolite_name><metabolite_name>Levothyroxine</metabolite_name><metabolite_name>LysoPE 18:0</metabolite_name><metabolite_name>19(R)-Hydroxy prostaglandin F2Ï«</metabolite_name><metabolite_name>Eicosapentaenoic acid</metabolite_name><metabolite_name>Lysopc 17:0</metabolite_name><metabolite_name>Mycophenolic acid</metabolite_name><metabolite_name>D-Xylonic Acid</metabolite_name><metabolite_name>4-Hydroxybutyric acid (GHB)</metabolite_name><metabolite_name>Dehydrocholic acid</metabolite_name><metabolite_name>D-(-)-Glutamine</metabolite_name><metabolite_name>5-Aminolevulinic acid</metabolite_name><metabolite_name>Caprylic acid</metabolite_name><metabolite_name>17(S)-HpDHA</metabolite_name><metabolite_name>Cortodoxone</metabolite_name><metabolite_name>(S)-Leucic acid</metabolite_name><metabolite_name>6-phospho-D-glucono-1,5-lactone</metabolite_name><metabolite_name>LPC 16:0</metabolite_name><metabolite_name>LPC 16:1</metabolite_name><metabolite_name>N2,N2-Dimethylguanosine</metabolite_name><metabolite_name>Lauric acid ethyl ester</metabolite_name><metabolite_name>Dehydroepiandrosterone</metabolite_name><metabolite_name>N-acetyl-L-ornithine</metabolite_name><metabolite_name>1-(4-Methoxyphenyl)-2-propanone</metabolite_name><metabolite_name>L-Malate</metabolite_name><metabolite_name>Gluconolactone</metabolite_name><metabolite_name>Isorhapontigenin</metabolite_name><metabolite_name>2-Phenylpropionic acid</metabolite_name><metabolite_name>4-[2-(2-oxo-1-imidazolidinyl)ethyl]-1lambda~6~,4-thiazinane-1,1-dione</metabolite_name><metabolite_name>LNAPE 16:0/N-20:0</metabolite_name><metabolite_name>N-Acetyl-DL-phenylalanine</metabolite_name><metabolite_name>Hippuric acid</metabolite_name><metabolite_name>15-OxoEDE</metabolite_name><metabolite_name>methadone-d9</metabolite_name><metabolite_name>N1-[3-(acetylamino)-2-oxo-2H-chromen-6-yl]-4-nitrobenzamide</metabolite_name><metabolite_name>Homovanillic acid</metabolite_name><metabolite_name>L-(-)-Glyceric acid</metabolite_name><metabolite_name>Triiodothyronine</metabolite_name><metabolite_name>2-Hydroxybutyric acid</metabolite_name><metabolite_name>Quinolinic acid</metabolite_name><metabolite_name>5-Methyluridine</metabolite_name><metabolite_name>D-Ala-D-Ala</metabolite_name><metabolite_name>JWH 018 N-pentanoic acid metabolite</metabolite_name><metabolite_name>Gly-Phe</metabolite_name><metabolite_name>D-Proline</metabolite_name><metabolite_name>Citraconic acid</metabolite_name><metabolite_name>Purine</metabolite_name><metabolite_name>Corchorifatty acid F</metabolite_name><metabolite_name>16-(Hexopyranosyloxy)-7-hydroxy-8,9-epoxypimaran-18-oic acid</metabolite_name><metabolite_name>Oxoadipic Acid</metabolite_name><metabolite_name>Glycerophospho-N-palmitoyl ethanolamine</metabolite_name><metabolite_name>Dl-3-Hydroxy-kynurenine</metabolite_name><metabolite_name>Cholic acid</metabolite_name><metabolite_name>Neohesperidin</metabolite_name><metabolite_name>Palmitic acid</metabolite_name><metabolite_name>Arachidonic acid</metabolite_name><metabolite_name>isoleucine</metabolite_name><metabolite_name>2,3-dinor Prostaglandin E1</metabolite_name><metabolite_name>PA 18:0_18:2</metabolite_name><metabolite_name>D-(+)-Mannose</metabolite_name><metabolite_name>16-Hydroxyhexadecanoic acid</metabolite_name><metabolite_name>alpha-D-Glucopyranosyl 2-O-(2-methylbutanoyl)-alpha-D-glucopyranoside</metabolite_name><metabolite_name>Ethylmalonic acid</metabolite_name><metabolite_name>3-[(methoxycarbonyl)amino]-2,2,3-trimethylbutanoic acid</metabolite_name><metabolite_name>13-Hpotre(R)</metabolite_name><metabolite_name>PG 18:1_18:1</metabolite_name><metabolite_name>4-Hydroxybenzoic acid</metabolite_name><metabolite_name>3-[3-(beta-D-Glucopyranosyloxy)-2-hydroxyphenyl]propanoic acid</metabolite_name><metabolite_name>Soyasaponin I</metabolite_name><metabolite_name>Maltotriose</metabolite_name><metabolite_name>N-Acetyl-1-aspartylglutamic acid</metabolite_name><metabolite_name>Valproic acid</metabolite_name><metabolite_name>Sebacic acid</metabolite_name><metabolite_name>N-Phenylacetylglutamine</metabolite_name><metabolite_name>Quercetin</metabolite_name><metabolite_name>PC 16:0_20:5</metabolite_name><metabolite_name>N4-Acetylcytidine</metabolite_name><metabolite_name>PC O-18:0_22:6</metabolite_name><metabolite_name>Nicotinamide</metabolite_name><metabolite_name>3-Methyl-2-oxobutanoic acid</metabolite_name><metabolite_name>Theophylline</metabolite_name><metabolite_name>3-(3-Methoxyphenyl)propionic acid</metabolite_name><metabolite_name>(©I)5(6)-DiHET</metabolite_name><metabolite_name>Cyclohexylsulfamate</metabolite_name><metabolite_name>Ethylmalonate</metabolite_name><metabolite_name>3-Indoxyl sulphate</metabolite_name><metabolite_name>4-Methyl-2-Oxopentanoic Acid</metabolite_name><metabolite_name>3-Methylglutaric acid</metabolite_name><metabolite_name>LPC 22:6</metabolite_name><metabolite_name>2-Hydroxyvaleric acid</metabolite_name><metabolite_name>Quinoline-4-carboxylic acid</metabolite_name><metabolite_name>D-Glucarate</metabolite_name><metabolite_name>Thr-Leu</metabolite_name><metabolite_name>N-Acetyl-DL-serine</metabolite_name><metabolite_name>2-{2-oxo-2-[(2-oxo-3-azepanyl)amino]ethoxy}acetic acid</metabolite_name><metabolite_name>Kynurenine</metabolite_name><metabolite_name>Luteolin</metabolite_name><metabolite_name>Ribulose-5-phosphate</metabolite_name><metabolite_name>(+/-)9,10-dihydroxy-12Z-octadecenoic acid</metabolite_name><metabolite_name>4-Methylphenol</metabolite_name><metabolite_name>Ascorbyl palmitate</metabolite_name><metabolite_name>Dodecanedioic acid</metabolite_name><metabolite_name>Ï«-Cyclodextrin</metabolite_name><metabolite_name>Xanthine</metabolite_name><metabolite_name>SM 8:1;2O/34:0</metabolite_name><metabolite_name>beta-Estradiol 17-Acetate</metabolite_name><metabolite_name>LPE 18:1</metabolite_name><metabolite_name>19(R)-hydroxy Prostaglandin A2</metabolite_name><metabolite_name>Ï«-D-Glucose-1,6-bisphosphate</metabolite_name><metabolite_name>LPE 18:3</metabolite_name><metabolite_name>L-Threonic acid Calcium Salt</metabolite_name><metabolite_name>Deoxyguanosine diphosphate (dGDP)</metabolite_name><metabolite_name>FAHFA 14:0/16:2</metabolite_name><metabolite_name>Aldosterone</metabolite_name><metabolite_name>3-Hydroxysebacic acid</metabolite_name><metabolite_name>D-Fructose 6-phosphate</metabolite_name><metabolite_name>L-Glutathione (reduced)</metabolite_name><metabolite_name>Nicotinamide N-oxide</metabolite_name><metabolite_name>LPC O-16:0</metabolite_name><metabolite_name>LPC O-16:1</metabolite_name><metabolite_name>13,14-dihydro-15-keto-tetranor Prostaglandin D2</metabolite_name><metabolite_name>LNAPE 22:4/N-18:0</metabolite_name><metabolite_name>2-[(4,6-dichloro-1,3-benzothiazol-2-yl)thio]aniline</metabolite_name><metabolite_name>Gluconic acid</metabolite_name><metabolite_name>Inositol</metabolite_name><metabolite_name>7-Methylxanthine</metabolite_name><metabolite_name>N-Acetylglycine</metabolite_name><metabolite_name>1,7-Bis(4-hydroxyphenyl)-3,5-heptanediol</metabolite_name><metabolite_name>2-Hydroxy-3-methylbutanoic acid</metabolite_name><metabolite_name>ethyl 4-chloro-3-[(3,5-dichloro-2-hydroxybenzylidene)amino]benzoate</metabolite_name><metabolite_name>N-Acetyl-D-alloisoleucine</metabolite_name><metabolite_name>Erythronolactone</metabolite_name><metabolite_name>Phenobarbital</metabolite_name><metabolite_name>diethyl 2-{[2-(2,4-dichlorophenoxy)anilino]methylidene}malonate</metabolite_name><metabolite_name>Dl-Lanthionine</metabolite_name><metabolite_name>2-Hydroxybenzaldehyde N-(4,6-dichloro-1,3-benzothiazol-2-yl)hydrazone</metabolite_name><metabolite_name>Thiodiglycolic acid</metabolite_name><metabolite_name>1a,1b-Dihomo prostaglandin E1</metabolite_name><metabolite_name>Lipoic acid</metabolite_name><metabolite_name>albiflorin</metabolite_name><metabolite_name>3-Oxo-7alpha,12alpha-hydroxy-5beta-cholanoic acid</metabolite_name><metabolite_name>PC O-18:1_16:0</metabolite_name><metabolite_name>Azelaic acid</metabolite_name><metabolite_name>2-(Dimethylamino)Guanosine</metabolite_name><metabolite_name>SM 8:1;2O/24:0</metabolite_name><metabolite_name>O1-[4-(tert-butyl)benzoyl]-2-(tert-butylsulfonyl)ethanehydroximamide</metabolite_name><metabolite_name>Dimetghyl 4-Hydroxyisophthalate</metabolite_name><metabolite_name>5-Methoxyindole-3-Carbaldehyde</metabolite_name><metabolite_name>2-Hydroxy-4-methylthiobutanoic acid</metabolite_name><metabolite_name>PC O-16:1_22:6</metabolite_name><metabolite_name>Rutin</metabolite_name><metabolite_name>Deoxycholic acid</metabolite_name><metabolite_name>Glycodeoxycholic acid</metabolite_name><metabolite_name>Estrone</metabolite_name><metabolite_name>D-2-Aminoadipic acid</metabolite_name><metabolite_name>Biopterin</metabolite_name><metabolite_name>N1-[4-(2-thienylthio)phenyl]-4-chlorobenzamide</metabolite_name><metabolite_name>Mestranol</metabolite_name><metabolite_name>LPE 16:0</metabolite_name><metabolite_name>2-Methoxyestradiol (2-MeOE2)</metabolite_name><metabolite_name>N1-(2-methyl-4-nitrophenyl)acetamide</metabolite_name></additional><is_claimable>false</is_claimable><name>Characterization Epstein-Barr Virus-Associated Encephalitis via Identification of Metabolomic Biomarkers</name><description>&lt;p>Objective:&amp;nbsp;Fulminant Epstein-Barr Virus (EBV) infection may lead to fatal outcomes in patients with EBV-associated encephalitis (EBVAE). To investigate potential&amp;nbsp;biomarkers in EBVAE, we utilized an untargeted metabolomic methodology to identify disease-associated biomarkers in patients with EBVAE.&amp;nbsp;&lt;/p>&lt;p>Methods:&amp;nbsp;Cerebrospinal fluid (CSF) from 15 patients with EBVAE and 6 control subjects with functional neurological disorders were collected and analyzed utilizing untargeted metabolomics. Metabolites were annotated, clustered, and subjected to statistical analysis.&lt;/p>&lt;p>Results:&amp;nbsp;Significant metabolomic alterations were observed between EBVAE patients and controls:&amp;nbsp;164&amp;nbsp;CSF metabolites were identified to be upregulated and&amp;nbsp;115&amp;nbsp;downregulated in patients with EBVAE. Among those, serotonin and tryptophan were markedly elevated in patients with EBVAE. Interestingly, 6 patients tested positive for glial fibrillary acidic protein (GFAP) antibodies in CSF met the criteria for GFAP-astrocytopathy (GFAP-A). Astrocytic&amp;nbsp;monoamine derivative methylphenyl ethylene glycol was significantly elevated in GFAP-A subgroup compared with GFAP Ab-negative group. 6 out of 15 patients with EBVAE progressed to acute disseminated encephalomyelitis (ADEM). Gamma-aminobutyric acid (GABA) was found to be negatively correlated with Glasgow Coma Scale (GCS) scores (r = -0.858, p &amp;lt; 0.001) in the ADEM subgroup.&lt;/p>&lt;p>Conclusion:&amp;nbsp;Our study first characterizes the metabolomic profile of patients with EBVAE, including those with EBV positive GFAP-A or ADEM.&amp;nbsp;&lt;/p></description><dates><publication>2026-03-23</publication><submission>2026-03-23</submission></dates><accession>MTBLS14111</accession><cross_references><KEGG>Com_27_pos</KEGG><KEGG>Com_28_pos</KEGG><KEGG>Com_35_pos</KEGG><KEGG>Com_39_pos</KEGG><KEGG>Com_50_pos</KEGG><KEGG>Com_54_pos</KEGG><KEGG>Com_64_pos</KEGG><KEGG>Com_70_pos</KEGG><KEGG>Com_76_pos</KEGG><KEGG>Com_82_pos</KEGG><KEGG>Com_89_pos</KEGG><KEGG>Com_107_pos</KEGG><KEGG>Com_137_pos</KEGG><KEGG>Com_183_pos</KEGG><KEGG>Com_211_pos</KEGG><KEGG>Com_221_pos</KEGG><KEGG>Com_304_pos</KEGG><KEGG>Com_321_pos</KEGG><KEGG>Com_373_pos</KEGG><KEGG>Com_375_pos</KEGG><KEGG>Com_391_pos</KEGG><KEGG>Com_404_pos</KEGG><KEGG>Com_516_pos</KEGG><KEGG>Com_548_pos</KEGG><KEGG>Com_562_pos</KEGG><KEGG>Com_565_pos</KEGG><KEGG>Com_573_pos</KEGG><KEGG>Com_606_pos</KEGG><KEGG>Com_612_pos</KEGG><KEGG>Com_729_pos</KEGG><KEGG>Com_738_pos</KEGG><KEGG>Com_781_pos</KEGG><KEGG>Com_793_pos</KEGG><KEGG>Com_806_pos</KEGG><KEGG>Com_940_pos</KEGG><KEGG>Com_1048_pos</KEGG><KEGG>Com_1156_pos</KEGG><KEGG>Com_1236_pos</KEGG><KEGG>Com_1259_pos</KEGG><KEGG>Com_1293_pos</KEGG><KEGG>Com_1486_pos</KEGG><KEGG>Com_1870_pos</KEGG><KEGG>Com_1988_pos</KEGG><KEGG>Com_2166_pos</KEGG><KEGG>Com_2463_pos</KEGG><KEGG>Com_2773_pos</KEGG><KEGG>Com_2990_pos</KEGG><KEGG>Com_2996_pos</KEGG><KEGG>Com_3837_pos</KEGG><KEGG>Com_4132_pos</KEGG><KEGG>Com_4248_pos</KEGG><KEGG>Com_4441_pos</KEGG><KEGG>Com_4462_pos</KEGG><KEGG>Com_4825_pos</KEGG><KEGG>Com_7938_pos</KEGG><KEGG>Com_7975_pos</KEGG><KEGG>Com_8364_pos</KEGG><KEGG>Com_8526_pos</KEGG><KEGG>Com_12474_pos</KEGG><KEGG>Com_12996_pos</KEGG><KEGG>Com_9_pos</KEGG><KEGG>Com_33_pos</KEGG><KEGG>Com_41_pos</KEGG><KEGG>Com_43_pos</KEGG><KEGG>Com_47_pos</KEGG><KEGG>Com_72_pos</KEGG><KEGG>Com_98_pos</KEGG><KEGG>Com_114_pos</KEGG><KEGG>Com_206_pos</KEGG><KEGG>Com_452_pos</KEGG><KEGG>Com_839_pos</KEGG><KEGG>Com_1105_pos</KEGG><KEGG>Com_1419_pos</KEGG><KEGG>Com_2096_pos</KEGG><KEGG>Com_2161_pos</KEGG><KEGG>Com_2193_pos</KEGG><KEGG>Com_2734_pos</KEGG><KEGG>Com_3311_pos</KEGG><KEGG>Com_3630_pos</KEGG><KEGG>Com_3750_pos</KEGG><KEGG>Com_5800_pos</KEGG><KEGG>Com_7700_pos</KEGG><KEGG>Com_22_pos</KEGG><KEGG>Com_23_pos</KEGG><KEGG>Com_36_pos</KEGG><KEGG>Com_49_pos</KEGG><KEGG>Com_56_pos</KEGG><KEGG>Com_68_pos</KEGG><KEGG>Com_80_pos</KEGG><KEGG>Com_96_pos</KEGG><KEGG>Com_102_pos</KEGG><KEGG>Com_127_pos</KEGG><KEGG>Com_131_pos</KEGG><KEGG>Com_153_pos</KEGG><KEGG>Com_158_pos</KEGG><KEGG>Com_162_pos</KEGG><KEGG>Com_175_pos</KEGG><KEGG>Com_246_pos</KEGG><KEGG>Com_249_pos</KEGG><KEGG>Com_252_pos</KEGG><KEGG>Com_263_pos</KEGG><KEGG>Com_271_pos</KEGG><KEGG>Com_282_pos</KEGG><KEGG>Com_311_pos</KEGG><KEGG>Com_327_pos</KEGG><KEGG>Com_337_pos</KEGG><KEGG>Com_338_pos</KEGG><KEGG>Com_345_pos</KEGG><KEGG>Com_363_pos</KEGG><KEGG>Com_367_pos</KEGG><KEGG>Com_400_pos</KEGG><KEGG>Com_428_pos</KEGG><KEGG>Com_429_pos</KEGG><KEGG>Com_446_pos</KEGG><KEGG>Com_458_pos</KEGG><KEGG>Com_482_pos</KEGG><KEGG>Com_510_pos</KEGG><KEGG>Com_511_pos</KEGG><KEGG>Com_519_pos</KEGG><KEGG>Com_538_pos</KEGG><KEGG>Com_593_pos</KEGG><KEGG>Com_609_pos</KEGG><KEGG>Com_647_pos</KEGG><KEGG>Com_656_pos</KEGG><KEGG>Com_670_pos</KEGG><KEGG>Com_703_pos</KEGG><KEGG>Com_718_pos</KEGG><KEGG>Com_730_pos</KEGG><KEGG>Com_743_pos</KEGG><KEGG>Com_747_pos</KEGG><KEGG>Com_750_pos</KEGG><KEGG>Com_756_pos</KEGG><KEGG>Com_779_pos</KEGG><KEGG>Com_780_pos</KEGG><KEGG>Com_794_pos</KEGG><KEGG>Com_808_pos</KEGG><KEGG>Com_825_pos</KEGG><KEGG>Com_827_pos</KEGG><KEGG>Com_881_pos</KEGG><KEGG>Com_903_pos</KEGG><KEGG>Com_905_pos</KEGG><KEGG>Com_920_pos</KEGG><KEGG>Com_927_pos</KEGG><KEGG>Com_941_pos</KEGG><KEGG>Com_944_pos</KEGG><KEGG>Com_945_pos</KEGG><KEGG>Com_1021_pos</KEGG><KEGG>Com_1037_pos</KEGG><KEGG>Com_1054_pos</KEGG><KEGG>Com_1075_pos</KEGG><KEGG>Com_1175_pos</KEGG><KEGG>Com_1207_pos</KEGG><KEGG>Com_1209_pos</KEGG><KEGG>Com_1215_pos</KEGG><KEGG>Com_1226_pos</KEGG><KEGG>Com_1243_pos</KEGG><KEGG>Com_1250_pos</KEGG><KEGG>Com_1255_pos</KEGG><KEGG>Com_1257_pos</KEGG><KEGG>Com_1288_pos</KEGG><KEGG>Com_1289_pos</KEGG><KEGG>Com_1296_pos</KEGG><KEGG>Com_1388_pos</KEGG><KEGG>Com_1405_pos</KEGG><KEGG>Com_1408_pos</KEGG><KEGG>Com_1412_pos</KEGG><KEGG>Com_1443_pos</KEGG><KEGG>Com_1481_pos</KEGG><KEGG>Com_1485_pos</KEGG><KEGG>Com_1498_pos</KEGG><KEGG>Com_1602_pos</KEGG><KEGG>Com_1629_pos</KEGG><KEGG>Com_1690_pos</KEGG><KEGG>Com_1709_pos</KEGG><KEGG>Com_1713_pos</KEGG><KEGG>Com_1783_pos</KEGG><KEGG>Com_1785_pos</KEGG><KEGG>Com_1797_pos</KEGG><KEGG>Com_1798_pos</KEGG><KEGG>Com_1825_pos</KEGG><KEGG>Com_1846_pos</KEGG><KEGG>Com_1880_pos</KEGG><KEGG>Com_1899_pos</KEGG><KEGG>Com_1918_pos</KEGG><KEGG>Com_1934_pos</KEGG><KEGG>Com_1939_pos</KEGG><KEGG>Com_1941_pos</KEGG><KEGG>Com_1948_pos</KEGG><KEGG>Com_1952_pos</KEGG><KEGG>Com_1958_pos</KEGG><KEGG>Com_1990_pos</KEGG><KEGG>Com_1991_pos</KEGG><KEGG>Com_2048_pos</KEGG><KEGG>Com_2076_pos</KEGG><KEGG>Com_2088_pos</KEGG><KEGG>Com_2114_pos</KEGG><KEGG>Com_2117_pos</KEGG><KEGG>Com_2172_pos</KEGG><KEGG>Com_2180_pos</KEGG><KEGG>Com_2203_pos</KEGG><KEGG>Com_2286_pos</KEGG><KEGG>Com_2296_pos</KEGG><KEGG>Com_2318_pos</KEGG><KEGG>Com_2340_pos</KEGG><KEGG>Com_2391_pos</KEGG><KEGG>Com_2408_pos</KEGG><KEGG>Com_2417_pos</KEGG><KEGG>Com_2443_pos</KEGG><KEGG>Com_2542_pos</KEGG><KEGG>Com_2547_pos</KEGG><KEGG>Com_2554_pos</KEGG><KEGG>Com_2568_pos</KEGG><KEGG>Com_2572_pos</KEGG><KEGG>Com_2582_pos</KEGG><KEGG>Com_2642_pos</KEGG><KEGG>Com_2669_pos</KEGG><KEGG>Com_2682_pos</KEGG><KEGG>Com_2685_pos</KEGG><KEGG>Com_2691_pos</KEGG><KEGG>Com_2735_pos</KEGG><KEGG>Com_2737_pos</KEGG><KEGG>Com_2760_pos</KEGG><KEGG>Com_2781_pos</KEGG><KEGG>Com_2791_pos</KEGG><KEGG>Com_2802_pos</KEGG><KEGG>Com_2809_pos</KEGG><KEGG>Com_2825_pos</KEGG><KEGG>Com_2872_pos</KEGG><KEGG>Com_2878_pos</KEGG><KEGG>Com_2916_pos</KEGG><KEGG>Com_2921_pos</KEGG><KEGG>Com_2958_pos</KEGG><KEGG>Com_2988_pos</KEGG><KEGG>Com_3038_pos</KEGG><KEGG>Com_3039_pos</KEGG><KEGG>Com_3094_pos</KEGG><KEGG>Com_3110_pos</KEGG><KEGG>Com_3221_pos</KEGG><KEGG>Com_3224_pos</KEGG><KEGG>Com_3241_pos</KEGG><KEGG>Com_3278_pos</KEGG><KEGG>Com_3284_pos</KEGG><KEGG>Com_3367_pos</KEGG><KEGG>Com_3378_pos</KEGG><KEGG>Com_3405_pos</KEGG><KEGG>Com_3420_pos</KEGG><KEGG>Com_3435_pos</KEGG><KEGG>Com_3436_pos</KEGG><KEGG>Com_3496_pos</KEGG><KEGG>Com_3504_pos</KEGG><KEGG>Com_3506_pos</KEGG><KEGG>Com_3527_pos</KEGG><KEGG>Com_3533_pos</KEGG><KEGG>Com_3541_pos</KEGG><KEGG>Com_3564_pos</KEGG><KEGG>Com_3584_pos</KEGG><KEGG>Com_3599_pos</KEGG><KEGG>Com_3605_pos</KEGG><KEGG>Com_3643_pos</KEGG><KEGG>Com_3647_pos</KEGG><KEGG>Com_3672_pos</KEGG><KEGG>Com_3692_pos</KEGG><KEGG>Com_3744_pos</KEGG><KEGG>Com_3767_pos</KEGG><KEGG>Com_3776_pos</KEGG><KEGG>Com_3777_pos</KEGG><KEGG>Com_3828_pos</KEGG><KEGG>Com_3840_pos</KEGG><KEGG>Com_3895_pos</KEGG><KEGG>Com_3948_pos</KEGG><KEGG>Com_3955_pos</KEGG><KEGG>Com_3962_pos</KEGG><KEGG>Com_4006_pos</KEGG><KEGG>Com_4041_pos</KEGG><KEGG>Com_4054_pos</KEGG><KEGG>Com_4057_pos</KEGG><KEGG>Com_4087_pos</KEGG><KEGG>Com_4122_pos</KEGG><KEGG>Com_4135_pos</KEGG><KEGG>Com_4174_pos</KEGG><KEGG>Com_4324_pos</KEGG><KEGG>Com_4347_pos</KEGG><KEGG>Com_4355_pos</KEGG><KEGG>Com_4378_pos</KEGG><KEGG>Com_4403_pos</KEGG><KEGG>Com_4406_pos</KEGG><KEGG>Com_4448_pos</KEGG><KEGG>Com_4506_pos</KEGG><KEGG>Com_4512_pos</KEGG><KEGG>Com_4537_pos</KEGG><KEGG>Com_4553_pos</KEGG><KEGG>Com_4598_pos</KEGG><KEGG>Com_4708_pos</KEGG><KEGG>Com_4719_pos</KEGG><KEGG>Com_4736_pos</KEGG><KEGG>Com_4747_pos</KEGG><KEGG>Com_4795_pos</KEGG><KEGG>Com_4921_pos</KEGG><KEGG>Com_4933_pos</KEGG><KEGG>Com_4963_pos</KEGG><KEGG>Com_5046_pos</KEGG><KEGG>Com_5052_pos</KEGG><KEGG>Com_5068_pos</KEGG><KEGG>Com_5084_pos</KEGG><KEGG>Com_5198_pos</KEGG><KEGG>Com_5203_pos</KEGG><KEGG>Com_5244_pos</KEGG><KEGG>Com_5251_pos</KEGG><KEGG>Com_5260_pos</KEGG><KEGG>Com_5392_pos</KEGG><KEGG>Com_5410_pos</KEGG><KEGG>Com_5426_pos</KEGG><KEGG>Com_5456_pos</KEGG><KEGG>Com_5458_pos</KEGG><KEGG>Com_5476_pos</KEGG><KEGG>Com_5507_pos</KEGG><KEGG>Com_5525_pos</KEGG><KEGG>Com_5539_pos</KEGG><KEGG>Com_5572_pos</KEGG><KEGG>Com_5638_pos</KEGG><KEGG>Com_5643_pos</KEGG><KEGG>Com_5661_pos</KEGG><KEGG>Com_5687_pos</KEGG><KEGG>Com_5723_pos</KEGG><KEGG>Com_5761_pos</KEGG><KEGG>Com_5803_pos</KEGG><KEGG>Com_5831_pos</KEGG><KEGG>Com_5912_pos</KEGG><KEGG>Com_5939_pos</KEGG><KEGG>Com_5966_pos</KEGG><KEGG>Com_5972_pos</KEGG><KEGG>Com_5991_pos</KEGG><KEGG>Com_6020_pos</KEGG><KEGG>Com_6039_pos</KEGG><KEGG>Com_6082_pos</KEGG><KEGG>Com_6109_pos</KEGG><KEGG>Com_6114_pos</KEGG><KEGG>Com_6144_pos</KEGG><KEGG>Com_6171_pos</KEGG><KEGG>Com_6194_pos</KEGG><KEGG>Com_6207_pos</KEGG><KEGG>Com_6227_pos</KEGG><KEGG>Com_6253_pos</KEGG><KEGG>Com_6276_pos</KEGG><KEGG>Com_6307_pos</KEGG><KEGG>Com_6324_pos</KEGG><KEGG>Com_6331_pos</KEGG><KEGG>Com_6357_pos</KEGG><KEGG>Com_6382_pos</KEGG><KEGG>Com_6388_pos</KEGG><KEGG>Com_6482_pos</KEGG><KEGG>Com_6535_pos</KEGG><KEGG>Com_6648_pos</KEGG><KEGG>Com_6678_pos</KEGG><KEGG>Com_6694_pos</KEGG><KEGG>Com_6705_pos</KEGG><KEGG>Com_6741_pos</KEGG><KEGG>Com_6748_pos</KEGG><KEGG>Com_6766_pos</KEGG><KEGG>Com_6772_pos</KEGG><KEGG>Com_6856_pos</KEGG><KEGG>Com_6881_pos</KEGG><KEGG>Com_6936_pos</KEGG><KEGG>Com_6954_pos</KEGG><KEGG>Com_7027_pos</KEGG><KEGG>Com_7050_pos</KEGG><KEGG>Com_7154_pos</KEGG><KEGG>Com_7159_pos</KEGG><KEGG>Com_7167_pos</KEGG><KEGG>Com_7172_pos</KEGG><KEGG>Com_7180_pos</KEGG><KEGG>Com_7205_pos</KEGG><KEGG>Com_7236_pos</KEGG><KEGG>Com_7276_pos</KEGG><KEGG>Com_7290_pos</KEGG><KEGG>Com_7327_pos</KEGG><KEGG>Com_7329_pos</KEGG><KEGG>Com_7339_pos</KEGG><KEGG>Com_7364_pos</KEGG><KEGG>Com_7371_pos</KEGG><KEGG>Com_7464_pos</KEGG><KEGG>Com_7498_pos</KEGG><KEGG>Com_7502_pos</KEGG><KEGG>Com_7524_pos</KEGG><KEGG>Com_7534_pos</KEGG><KEGG>Com_7541_pos</KEGG><KEGG>Com_7551_pos</KEGG><KEGG>Com_7613_pos</KEGG><KEGG>Com_7617_pos</KEGG><KEGG>Com_7721_pos</KEGG><KEGG>Com_7754_pos</KEGG><KEGG>Com_7766_pos</KEGG><KEGG>Com_7806_pos</KEGG><KEGG>Com_7814_pos</KEGG><KEGG>Com_7858_pos</KEGG><KEGG>Com_7860_pos</KEGG><KEGG>Com_7863_pos</KEGG><KEGG>Com_7875_pos</KEGG><KEGG>Com_7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