Whole genome amplification (WGA) for archiving and genotyping of clinical isolates of Cryptosporidium species

被引:11
作者
Bouzid, Maha [1 ]
Heavens, Darren [2 ]
Elwin, Kristin [3 ]
Chalmers, Rachel M. [3 ]
Hadfield, Stephen J. [3 ]
Hunter, Paul R. [1 ]
Tyler, Kevin M. [1 ]
机构
[1] Univ E Anglia, Biomed Res Ctr, Sch Med Hlth Policy & Practice, Norwich NR4 7TJ, Norfolk, England
[2] John Innes Ctr, Genome Lab, Norwich NR4 7UH, Norfolk, England
[3] Singleton Hosp, UK Cryptosporidium Reference Unit, NPHS Microbiol Swansea, Swansea SA2 8QA, W Glam, Wales
关键词
whole genome amplification; multi-displacement amplification; Cryptosporidium DNA; genotyping; MULTIPLE DISPLACEMENT AMPLIFICATION; PHI-29; DNA-POLYMERASE; SINGLE-CELL; PARVUM; PCR; HUMANS; IDENTIFICATION; QUANTITATION; TRANSMISSION; FIDELITY;
D O I
10.1017/S0031182009991132
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Clinical and environmental isolates of pathogens are often unique and may be unculturable, yielding a very limited amount of DNA for genetic Studies. Cryptosporidium in particular are difficult to propagate. Whole genome amplification (WGA) is a valuable technique for amplifying genomic material. In this study, we tested 5 WGA commercial kits using Cryptosporidium clinical isolates. DNA of 5 C. hominis and 5 C. parvum clinical isolates and C. parvum IOWA reference strain were used. The majority of the samples were amplified by all of the kits tested. The integrity and fidelity of the amplified genomic DNA were assessed by sequence analysis of several PCR products of varying length. We found evidence that one kit in particular may be more error prone while another seemed the more suitable kit for Cryptosporidium clinical samples, generating high molecular weight DNA from all the samples with high fidelity. Thus WGA was found to be a useful technique for producing amplified DNA Suitable for downstream genotyping techniques and archiving of Cryptosporidium clinical isolates.
引用
收藏
页码:27 / 36
页数:10
相关论文
共 40 条
[1]   PicoGreen quantitation of DNA: Effective evaluation of samples pre- or post-PCR [J].
Ahn, SJ ;
Costa, J ;
Emanuel, JR .
NUCLEIC ACIDS RESEARCH, 1996, 24 (13) :2623-2625
[2]   Microsatellite markers reveal a spectrum of population structures in the malaria parasite Plasmodium falciparum [J].
Anderson, TJC ;
Haubold, B ;
Williams, JT ;
Estrada-Franco, JG ;
Richardson, L ;
Mollinedo, R ;
Bockarie, M ;
Mokili, J ;
Mharakurwa, S ;
French, N ;
Whitworth, J ;
Velez, ID ;
Brockman, AH ;
Nosten, F ;
Ferreira, MU ;
Day, KP .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (10) :1467-1482
[3]   Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel [J].
Barker, DL ;
Hansen, MST ;
Faruqi, AF ;
Giannola, D ;
Irsula, OR ;
Lasken, RS ;
Latterich, M ;
Makarov, V ;
Oliphant, A ;
Pinter, JH ;
Shen, R ;
Sleptsova, I ;
Ziehler, W ;
Lai, E .
GENOME RESEARCH, 2004, 14 (05) :901-907
[4]   Comparison of yield and genotyping performance of multiple displacement OmniPlex™ whole genome amplified DNA generated from multiple DNA sources [J].
Bergen, AW ;
Haque, KA ;
Qi, Y ;
Beerman, MB ;
Garcia-Closas, M ;
Rothman, N ;
Chanock, SJ .
HUMAN MUTATION, 2005, 26 (03) :262-270
[5]  
BLANCO L, 1989, J BIOL CHEM, V264, P8935
[6]   Detection and surveillance of waterborne protozoan parasites [J].
Bouzid, Maha ;
Steverding, Dietmar ;
Tyler, Kevin M. .
CURRENT OPINION IN BIOTECHNOLOGY, 2008, 19 (03) :302-306
[7]  
Burgos Marcos V, 2004, Biomed., V24, P188
[8]   A microsatellite marker reveals population heterogeneity within human and animal genotypes of Cryptosporidium parvum [J].
Cacciò, S ;
Homan, W ;
Camilli, R ;
Traldi, G ;
Kortbeek, T ;
Pozio, E .
PARASITOLOGY, 2000, 120 :237-244
[9]   Molecular characterization of the Cryptosporidium parvum IOWA isolate kept in different laboratories [J].
Cama, Vitaliano A. ;
Arrowood, Michael J. ;
Ortega, Ynes R. ;
Xiao, Lihua .
JOURNAL OF EUKARYOTIC MICROBIOLOGY, 2006, 53 :S40-S42
[10]   Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA [J].
Cheung, VG ;
Nelson, SF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14676-14679