1.Study on high throughput sequencing identification of Fructus Arctii and five counterfeit species mix power.
Yan-Ping XING ; Si-You CHEN ; Liang XU ; Yong-Man LIANG ; Jia-Hao WANG ; Bing WANG ; Tao LIU ; Ting-Guo KANG
China Journal of Chinese Materia Medica 2018;43(19):3862-3866
Fructus Arctii is a traditional Chinese medicine. The main counterfeit species are the seeds of Arctium tomentosum, Onopordum acanthium, Silybum marianum, Saussurea costus, Amorpha fruticosa. Traditional identification methods or molecular barcoding techniques can identify Fructus Arctii and its counterfeit species. However, the identification of the mixture of it and its spurious species is rarely reported. In this paper, we sequenced the ITS2 sequences of Fructus Arctii and 5 kinds of spurious species mix powder by high-throughput sequencing to identify the mixed powder species and providing new ideas for the identification of Fructus Arctii mix powder. The total DNA in mixed powder was extracted, and the ITS2 sequences in total DNA was amplified. Paired-end sequencing was performed on the DNA fragment of the community using the Illumina MiSeq platform. The sequence was analyzed by the software FLASH, QIIME and GraPhlAn etc. The results showed that the high quality ITS2 sequences of 39910 mix samples were obtained from the mixed samples, of which the total ITS2 sequence of the samples genus was 34 935. Phylogenetic analysis showed that the samples contained Fructus Arctii, A. tomentosum, O. acanthium, S. marianum, S. costus and A. fruticosa. Using ITS2 sequences as DNA barcodes, high-throughput sequencing technology can be used to detect the Fructus Arctii and its spurious specie in mixed powder, which can provide reference for the quality control, safe use of medicinal materials of Fructus Arctii and the identification of mixed powder of traditional Chinese medicine.
Arctium
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chemistry
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classification
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DNA Barcoding, Taxonomic
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DNA, Plant
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genetics
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DNA, Ribosomal Spacer
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genetics
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Drug Contamination
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Drugs, Chinese Herbal
;
standards
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Fabaceae
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Fruit
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High-Throughput Nucleotide Sequencing
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Milk Thistle
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Onopordum
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Phylogeny
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Saussurea
2.First Case Report of Bacteremia Due to Catabacter hongkongensis in a Korean Patient.
Yong Jun CHOI ; Eun Jeong WON ; Soo Hyun KIM ; Myung Geun SHIN ; Jong Hee SHIN ; Soon Pal SUH
Annals of Laboratory Medicine 2017;37(1):84-87
No abstract available.
Aged
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Anti-Bacterial Agents/pharmacology/therapeutic use
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Cefotaxime/analogs & derivatives/therapeutic use
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Cholangiopancreatography, Endoscopic Retrograde
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Gallstones/surgery
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Gram-Negative Anaerobic Bacteria/drug effects/genetics/*isolation & purification
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Gram-Negative Bacterial Infections/*diagnosis/drug therapy/microbiology
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Humans
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Male
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Metronidazole/therapeutic use
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Microbial Sensitivity Tests
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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Sequence Analysis, DNA
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Tomography, X-Ray Computed
3.Analysis of the Vaginal Microbiome by Next-Generation Sequencing and Evaluation of its Performance as a Clinical Diagnostic Tool in Vaginitis.
Ki Ho HONG ; Sung Kuk HONG ; Sung Im CHO ; Eunkyung RA ; Kyung Hee HAN ; Soon Beom KANG ; Eui Chong KIM ; Sung Sup PARK ; Moon Woo SEONG
Annals of Laboratory Medicine 2016;36(5):441-449
BACKGROUND: Next-generation sequencing (NGS) can detect many more microorganisms of a microbiome than traditional methods. This study aimed to analyze the vaginal microbiomes of Korean women by using NGS that included bacteria and other microorganisms. The NGS results were compared with the results of other assays, and NGS was evaluated for its feasibility for predicting vaginitis. METHODS: In total, 89 vaginal swab specimens were collected. Microscopic examinations of Gram staining and microbiological cultures were conducted on 67 specimens. NGS was performed with GS junior system on all of the vaginal specimens for the 16S rRNA, internal transcribed spacer (ITS), and Tvk genes to detect bacteria, fungi, and Trichomonas vaginalis. In addition, DNA probe assays of the Candida spp., Gardnerella vaginalis, and Trichomonas vaginalis were performed. Various predictors of diversity that were obtained from the NGS data were analyzed to predict vaginitis. RESULTS: ITS sequences were obtained in most of the specimens (56.2%). The compositions of the intermediate and vaginitis Nugent score groups were similar to each other but differed from the composition of the normal score group. The fraction of the Lactobacillus spp. showed the highest area under the curve value (0.8559) in ROC curve analysis. The NGS and DNA probe assay results showed good agreement (range, 86.2-89.7%). CONCLUSIONS: Fungi as well as bacteria should be considered for the investigation of vaginal microbiome. The intermediate and vaginitis Nugent score groups were indistinguishable in NGS. NGS is a promising diagnostic tool of the vaginal microbiome and vaginitis, although some problems need to be resolved.
Area Under Curve
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Bacteria/*genetics/isolation & purification
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Bacterial Proteins/genetics
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Candida/*genetics/isolation & purification
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Female
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Fungal Proteins/genetics
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Gardnerella vaginalis/genetics/isolation & purification
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High-Throughput Nucleotide Sequencing
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Humans
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*Microbiota
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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ROC Curve
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Sequence Analysis, DNA
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Trichomonas vaginalis/genetics/isolation & purification
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Vagina/*microbiology
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Vaginitis/*diagnosis/microbiology
4.Fusobacterium Isolates Recovered From Colonic Biopsies of Inflammatory Bowel Disease Patients in Korea.
Yangsoon LEE ; Chang Soo EUN ; A Reum LEE ; Chan Hyuk PARK ; Dong Soo HAN
Annals of Laboratory Medicine 2016;36(4):387-389
No abstract available.
Adult
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Aged
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Biopsy
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Colon/*microbiology/pathology
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Fusobacterium/genetics/*isolation & purification
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Humans
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Inflammatory Bowel Diseases/microbiology/*pathology
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Male
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Middle Aged
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Polymerase Chain Reaction
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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Republic of Korea
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Sequence Analysis, DNA
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Young Adult
5.Identification of Pasteurella canis in a Soft Tissue Infection Caused by a Dog Bite: The First Report in Korea.
Bongyoung KIM ; Hyunjoo PAI ; Kwang hyun LEE ; Yangsoon LEE
Annals of Laboratory Medicine 2016;36(6):617-619
No abstract available.
Animals
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Anti-Bacterial Agents/pharmacology
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Bites and Stings
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Disk Diffusion Antimicrobial Tests
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Dogs
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Female
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Humans
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Middle Aged
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Pasteurella/drug effects/genetics/*isolation & purification
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Pasteurella Infections/*diagnosis/microbiology
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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Republic of Korea
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Sequence Analysis, DNA
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Soft Tissue Infections/*diagnosis/microbiology
6.Flavobacterium ceti From Blood Samples of a Korean Patient With Alcoholic Liver Cirrhosis.
Ji Yeon SUNG ; Taek Soo KIM ; Sue SHIN ; Eun Youn ROH ; Jong Hyun YOON ; Eui Chong KIM
Annals of Laboratory Medicine 2015;35(3):384-386
No abstract available.
Asian Continental Ancestry Group
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Flavobacteriaceae Infections
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Flavobacterium/*genetics/isolation & purification
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Humans
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Liver Cirrhosis, Alcoholic/blood/*diagnosis/microbiology
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Male
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Middle Aged
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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Republic of Korea
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Sequence Analysis, DNA
7.First Case of Pulmonary Mycobacterium parascrofulaceum Infection in a Patient With Bronchiectasis in Korea.
Kyoung Bo KIM ; Sung Gyun PARK ; Jae Seok PARK ; Wonmok LEE ; Jung Sook HA ; Nam Hee RYOO ; Dong Seok JEON ; Jae Ryong KIM
Annals of Laboratory Medicine 2015;35(3):379-381
No abstract available.
Aged
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Bronchiectasis/*diagnosis/microbiology
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Humans
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Male
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Mycobacterium/classification/*genetics/isolation & purification
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Mycobacterium Infections/*diagnosis/microbiology
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Phylogeny
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Polymerase Chain Reaction
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RNA, Ribosomal, 16S/chemistry/genetics/metabolism
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Republic of Korea
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Sequence Analysis, DNA
8.Ancient Mitochondrial DNA Analyses of Ascaris Eggs Discovered in Coprolites from Joseon Tomb.
Chang Seok OH ; Min SEO ; Jong Ha HONG ; Jong Yil CHAI ; Seung Whan OH ; Jun Bum PARK ; Dong Hoon SHIN
The Korean Journal of Parasitology 2015;53(2):237-242
Analysis of ancient DNA (aDNA) extracted from Ascaris is very important for understanding the phylogenetic lineage of the parasite species. When aDNAs obtained from a Joseon tomb (SN2-19-1) coprolite in which Ascaris eggs were identified were amplified with primers for cytochrome b (cyt b) and 18S small subunit ribosomal RNA (18S rRNA) gene, the outcome exhibited Ascaris specific amplicon bands. By cloning, sequencing, and analysis of the amplified DNA, we obtained information valuable for comprehending genetic lineage of Ascaris prevalent among pre-modern Joseon peoples.
Adult
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Animals
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Ascariasis/diagnosis/history/*parasitology
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Ascaris/classification/genetics/*isolation & purification
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Base Sequence
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Cytochromes b/genetics
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DNA Primers/genetics
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DNA, Helminth/*genetics
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DNA, Mitochondrial/*genetics/history
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Female
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Fossils/history/parasitology
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History, Ancient
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Humans
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Male
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Molecular Sequence Data
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Mummies/history/*parasitology
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Ovum/chemistry/classification
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Phylogeny
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RNA, Ribosomal, 18S/genetics
9.The First Case of Concurrent Infective Endocarditis and Spondylitis Caused by Streptococcus tigurinus.
Borahm KIM ; Hee Jae HUH ; Doo Ryeon CHUNG ; Wook Sung KIM ; Chang Seok KI ; Nam Yong LEE
Annals of Laboratory Medicine 2015;35(6):654-656
No abstract available.
Acupuncture Therapy
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Aged
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DNA/chemistry/genetics/metabolism
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Echocardiography
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Endocarditis/*diagnosis/microbiology
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Humans
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Magnetic Resonance Imaging
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Male
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Polymerase Chain Reaction
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RNA, Ribosomal, 16S/genetics/metabolism
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Sequence Analysis, DNA
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Spondylitis/*diagnosis/microbiology
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Streptococcus/*genetics/isolation & purification
10.Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns.
Xuejing SUN ; Zuoming XI ; Jing ZHANG ; Baoyan LIU ; Xinli XING ; Xin HUANG ; Qing ZHAO
Chinese Journal of Medical Genetics 2015;32(6):766-770
OBJECTIVETo evaluate the efficacy of combined newborn hearing screening and deafness-related mutation screening.
METHODSEleven thousand and forty-six newborn babies were screened with otoacoustic emission, automatic auditory brainstem response and genetic testing using a standard protocol. Common mutations of three deafness-related genes have included GJB2 (c.235delC, c.299-300delAT), mtDNA 12srRNA (c.1494C>T, c.1555A>G) and SLC26A4 (c.2168A>G, c.IVS7-2A>G).
RESULTSThe detection rate for hearing loss in the first-step screening was 0.81% (90/11,046). 513 individuals were found to carry one or two mutant alleles, which gave a carrier rate of 4.64% (513/11,046). Five hundred and eighty-four newborns were positive for hearing screening and genetic screening. Among these, 19 have failed both tests, 71 have failed hearing screening, and 494 have failed genetic screening. The combined hearing and genetic screening has given a positive rate of 5.29%.
CONCLUSIONNeither hearing screening nor genetic screening is sufficient to identify individuals susceptible to auditory disorders. Combined used of these methods can improve the rate of detection.
Asian Continental Ancestry Group ; genetics ; China ; Connexin 26 ; Connexins ; genetics ; DNA Mutational Analysis ; DNA, Mitochondrial ; chemistry ; genetics ; Deafness ; diagnosis ; ethnology ; genetics ; Gene Frequency ; Genetic Predisposition to Disease ; ethnology ; genetics ; Genetic Testing ; methods ; Genotype ; Hearing ; genetics ; Hearing Tests ; Humans ; Infant, Newborn ; Membrane Transport Proteins ; genetics ; Mutation ; Neonatal Screening ; methods ; Polymerase Chain Reaction ; RNA, Ribosomal ; genetics ; Reproducibility of Results ; Sensitivity and Specificity

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