McNulty Samantha N, Weil Gary J, Heinz Michael, Crosby Seth D, Fischer Peter U
Internal Medicine/Infectious Diseases Division, Washington University School of Medicine, Campus Mailbox 8051, 660 S. Euclid Avenue, St. Louis, MO 63110, USA.
Exp Parasitol. 2008 Jun;119(2):256-63. doi: 10.1016/j.exppara.2008.02.003. Epub 2008 Feb 19.
Genetic characterization of field isolates and clinical specimens of filarial nematodes is often limited by a shortage of DNA; therefore, we evaluated a multiple displacement amplification (MDA) based whole genome amplification method. The quality of amplified DNA was examined by conventional PCR, real-time PCR, and DNA hybridization. MDA of 5.0 ng of adult Brugia malayi DNA and one-fifteenth of the DNA isolated from a single microfilaria resulted in 6.3 and 4.2 microg of amplified DNA, respectively. Amplified DNA was equivalent to native genomic DNA for hybridization to B. malayi BAC library clones or to an oligonucleotide microarray with approximately 18,000 filarial DNA sequences. MDA is useful for whole genome amplification of filarial DNA from very small amounts of starting material. This technology will permit detailed studies of genetic diversity that were not previously feasible.
丝状线虫野外分离株和临床标本的基因特征分析常常因DNA短缺而受到限制;因此,我们评估了一种基于多重置换扩增(MDA)的全基因组扩增方法。通过常规PCR、实时PCR和DNA杂交检测扩增DNA的质量。对5.0 ng马来布鲁线虫成虫DNA以及从单个微丝蚴分离的DNA的十五分之一进行MDA,分别产生了6.3 μg和4.2 μg的扩增DNA。扩增DNA与马来布鲁线虫BAC文库克隆或与含有约18,000个丝状DNA序列的寡核苷酸微阵列杂交时,等同于天然基因组DNA。MDA可用于从极少量起始材料中对丝状DNA进行全基因组扩增。这项技术将使以前无法进行的遗传多样性详细研究成为可能。