Rapid and reasonable molecular identification of bacteria and fungi in microbiological diagnostics using rapid real-time PCR and Sanger sequencing

被引:12
|
作者
Sting, Reinhard [1 ]
Eisenberg, Tobias [2 ]
Hrubenja, Maja [1 ]
机构
[1] Chem & Vet Invest Off Stuttgart CVUAS, Schaflandstr 3-3, D-70736 Fellbach, Germany
[2] Hessian State Lab, Schubertstr 60, D-35392 Giessen, Germany
关键词
DNA sequencing; 16S rRNA gene; rpoB gene; ITS1/2; region; LSU D1/D2 region; 16S RIBOSOMAL-RNA; INTERNAL TRANSCRIBED SPACER; LARGE-SUBUNIT; REGION; AMPLIFICATION; DATABASE; GENES; D1/D2; RDNA;
D O I
10.1016/j.mimet.2019.03.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Analyses of short subunit gene sequences have been established for taxonomic classification and identification of bacteria and fungi. To produce partial bacterial ribosomal 16S rRNA and rpoB and fungal ribosomal ITS/LSU gene sequences for DNA sequencing, real-time PCR assays supplemented with the nucleic acid stain SYBR Green were created. Generation of PCR products was monitored based on amplification and melting curves. The PCR products were subsequently subjected to Sanger sequencing on demand for identification of bacteria and fungi in routine microbiological diagnostics within a period of two days. From a total of 78 bacterial isolates 40 (51%) or 67 (86%) could be identified at species level using only partial 16S rRNA or additionally rpoB gene sequences based on BLASTN (NCBI) database queries, respectively. Using partial 16S rRNA and rpoB gene sequencing unambiguous assignment was not possible for the closely related species of the Bacillus (B.) cereus group, Bordetella (B.) pertussis/B. parapertussis/B. bronchiseptica, Brucella spp., Enterobacter cloacae complex, Escherichia/Shigella spp., Staphylococcus (S.) hyicus/S. agnetis and Yersinia (Y.) pseudotuberculosis/Y. pestis. However, partial rpoB gene sequencing succeeded in identifying 27 bacterial isolates at species level in addition to 16S rRNA gene sequencing. Regarding ITS/LSU gene sequencing, best results could be achieved by ITS gene sequencing followed by LSU gene sequencing, resulting in 32 (63%) and 21 (43%) of a total of 51 fungal isolates that could be identified at species level, respectively. Insufficient identification at species level was observed for the genera Apiotrichum, Aspergillus, Cladosporium, Cryptococcus, Microsporum, Nannizziopsis, Penicillium, Trichosporon, and Tolypocladium included in this study. The concept of this procedure is suitable for rapid and reasonable molecular identification of bacteria and fungi within two days and is therefore applicable in routine microbiological diagnostic laboratories.
引用
收藏
页码:148 / 156
页数:9
相关论文
共 50 条
  • [1] Rapid Molecular Identification and Quantification of Allergenic Pollen By Real-Time PCR
    Teng, Michael
    Glaum, Mark C.
    Ledford, Dennis K.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2016, 137 (02) : AB119 - AB119
  • [2] Using real-time PCR as strategy to evaluate performance of PCR and Sanger sequencing reactions
    Freire-Paspuel, B.
    Burgos, G.
    FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, 2019, 7 (01) : 532 - 533
  • [3] Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
    Jung, Ju Yeon
    Yoon, Hyun Kyu
    An, Sanghyun
    Lee, Jee Won
    Ahn, Eu-Ree
    Kim, Yeon-Ji
    Park, Hyun-Chul
    Lee, Kyungmyung
    Hwang, Jung Ho
    Lim, Si-Keun
    SCIENTIFIC REPORTS, 2018, 8
  • [4] Rapid oral bacteria detection based on real-time PCR for the forensic identification of saliva
    Ju Yeon Jung
    Hyun Kyu Yoon
    Sanghyun An
    Jee Won Lee
    Eu-Ree Ahn
    Yeon-Ji Kim
    Hyun-Chul Park
    Kyungmyung Lee
    Jung Ho Hwang
    Si-Keun Lim
    Scientific Reports, 8
  • [5] Real-time PCR and its application for rapid plant disease diagnostics
    Schaad, NW
    Frederick, RD
    CANADIAN JOURNAL OF PLANT PATHOLOGY, 2002, 24 (03) : 250 - 258
  • [6] Rapid, multiplex and automated detection of bacteria and fungi in endophthalmitis via a microfluidic real-time pcr system
    Wang, Siyu
    Liu, Yiteng
    Li, Yingqi
    Gao, Yibo
    Zou, Zhongliang
    Xu, Na
    Song, Qi
    Liu, Fangyan
    Song, Yihong
    Wang, Xian
    Fan, Zixin
    JOURNAL OF OPHTHALMIC INFLAMMATION AND INFECTION, 2024, 14 (01):
  • [7] Rapid species identification of cooked poisonous mushrooms by using real-time PCR
    Maeta, Kazuhiko
    Ochi, Tomoya
    Tokimoto, Keisuke
    Shimomura, Norihiro
    Maekawa, Nitaro
    Kawaguchi, Nobuhisa
    Nakaya, Makoto
    Kitamoto, Yutaka
    Aimi, Tadanori
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2008, 74 (10) : 3306 - 3309
  • [8] Real-Time PCR and Sequencing Assays for Rapid Detection and Identification of Avian Schistosomes in Environmental Samples
    Jothikumar, Narayanan
    Mull, Bonnie J.
    Brant, Sara V.
    Loker, Eric S.
    Collinson, Jeremy
    Secor, W. Evan
    Hill, Vincent R.
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2015, 81 (12) : 4207 - 4215
  • [9] Rapid identification of Leishmania complexes by a real-time PCR assay
    Wortmann, G
    Hochberg, L
    Houng, HH
    Sweeney, C
    Zapor, M
    Aronson, N
    Weina, P
    Ockenhouse, CF
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2005, 73 (06): : 999 - 1004
  • [10] Rapid identification of bacteria by real-time amplification and sequencing of the 16S rRNA gene
    Vliegen, Inge
    Jacobs, Jan A.
    Beuken, Erik
    Bruggeman, Cathrien A.
    Vink, Cornelis
    JOURNAL OF MICROBIOLOGICAL METHODS, 2006, 66 (01) : 156 - 164