Quantitative CrAssphage real-time PCR assay derived from data of multiple geographically distant populations

被引:32
作者
Cinek, Ondrej [1 ,2 ]
Mazankova, Karla [1 ,2 ]
Kramna, Lenka [1 ,2 ]
Odeh, Rasha [3 ]
Alassaf, Abeer [3 ]
Ibekwe, MaryAnn U. [4 ]
Ahmadov, Gunduz [5 ]
Mekki, Hanan [6 ]
Abdullah, Mohammed A. [6 ,7 ]
Elmahi, Bashir M. E. [6 ,7 ]
Hyoety, Heikki [8 ,9 ]
Rainetova, Petra [10 ]
机构
[1] Charles Univ Prague, Dept Pediat, Fac Med 2, Prague, Czech Republic
[2] Univ Hosp Motol, Prague, Czech Republic
[3] Univ Jordan, Dept Pediat, Sch Med, Amman, Jordan
[4] Ebonyi State Univ, Dept Pediat, Abakaliki, Nigeria
[5] Azerbaijan Med Univ, Baku, Azerbaijan
[6] Univ Khartoum, Dept Paediat & Child Hlth, Fac Med, Khartoum, Sudan
[7] Sudan Childhood Diabet Ctr, Khartoum, Sudan
[8] Univ Tampere, Fac Med & Life Sci, Dept Virol, Tampere, Finland
[9] Pirkanmaa Hosp Dist, Fimlab Labs, Tampere, Finland
[10] Natl Inst Publ Hlth, Ctr Epidemiol & Microbiol, Prague, Czech Republic
关键词
Africa; Asia; polymorphism; virome; HUMAN FECAL POLLUTION; ISLET AUTOIMMUNITY; CHILDREN; SAMPLES;
D O I
10.1002/jmv.25012
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
After its computational inference from human stool metagenomes, the CrAssphage has proven to be the most prevalent phage in the human gut, with presumably very wide geographic distribution. The currently available molecular assays do not sufficiently reflect the CrAssphage sequence variability. Here, we report a novel real-time PCR assay whose primers and probes are derived from data of multiple CrAssphage strains obtained from gut viral metagenomes of European, Asian, and African subjects. This assay can be useful in analyses of putative bacterial host co-occurence, and in association studies of non-infectious diseases where the phage may modify the content of gut bacteriomes.
引用
收藏
页码:767 / 771
页数:5
相关论文
共 8 条
[1]   Imbalance of bacteriome profiles within the Finnish Diabetes Prediction and Prevention study: Parallel use of 16S profiling and virome sequencing in stool samples from children with islet autoimmunity and matched controls [J].
Cinek, Ondrej ;
Kramna, Lenka ;
Lin, Jake ;
Oikarinen, Sami ;
Kolarova, Katerina ;
Ilonen, Jorma ;
Simell, Olli ;
Veijola, Riitta ;
Autio, Reija ;
Hyoty, Heikki .
PEDIATRIC DIABETES, 2017, 18 (07) :588-598
[2]   A highly abundant bacteriophage discovered in the unknown sequences of human faecal metagenomes [J].
Dutilh, Bas E. ;
Cassman, Noriko ;
McNair, Katelyn ;
Sanchez, Savannah E. ;
Silva, Genivaldo G. Z. ;
Boling, Lance ;
Barr, Jeremy J. ;
Speth, Daan R. ;
Seguritan, Victor ;
Aziz, Ramy K. ;
Felts, Ben ;
Dinsdale, Elizabeth A. ;
Mokili, John L. ;
Edwards, Robert A. .
NATURE COMMUNICATIONS, 2014, 5
[3]  
Dutilh BE., 2014, BACTERIOPHAGE, V4, DOI DOI 10.4161/21597081.2014.979664
[4]   Determination of crAssphage in water samples and applicability for tracking human faecal pollution [J].
Garcia-Aljaro, Cristina ;
Balleste, Elisenda ;
Muniesa, Maite ;
Jofre, Juan .
MICROBIAL BIOTECHNOLOGY, 2017, 10 (06) :1775-1780
[5]   Gut Virome Sequencing in Children With Early Islet Autoimmunity [J].
Kramna, Lenka ;
Kolarova, Katerina ;
Oikarinen, Sami ;
Pursiheimo, Juha-Pekka ;
Ilonen, Jorma ;
Simell, Olli ;
Knip, Mikael ;
Veijola, Riitta ;
Hyoty, Heikki ;
Cinek, Ondrej .
DIABETES CARE, 2015, 38 (05) :930-933
[6]   crAssphage is not associated with diarrhoea and has high genetic diversity [J].
Liang, Y. Y. ;
Zhang, W. ;
Tong, Y. G. ;
Chen, S. P. .
EPIDEMIOLOGY AND INFECTION, 2016, 144 (16) :3549-3553
[7]   Development and application of a real-time polymerase chain reaction assay for detection of a novel gut bacteriophage (crAssphage) [J].
Liang, Yuying ;
Jin, Xin ;
Huang, Yuan ;
Chen, Shuiping .
JOURNAL OF MEDICAL VIROLOGY, 2018, 90 (03) :464-468
[8]   Quantitative CrAssphage PCR Assays for Human Fecal Pollution Measurement [J].
Stachler, Elyse ;
Kelty, Catherine ;
Sivaganesan, Mano ;
Li, Xiang ;
Bibby, Kyle ;
Shanks, Orin C. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2017, 51 (16) :9146-9154