Centre for Biotechnology, Anna University, Guindy, Chennai, Tamil Nadu 600025, India.
Infect Genet Evol. 2010 May;10(4):591-4. doi: 10.1016/j.meegid.2010.01.012. Epub 2010 Feb 2.
Polymerase chain reaction based methods are promising tools for the monitoring and evaluation of the Global Program for the Elimination of Lymphatic Filariasis. The currently available PCR methods do not differentiate the DNA of Wuchereria bancrofti or Brugia malayi by a single PCR and hence are cumbersome. Therefore, we designed a single step PCR strategy for differentiating Bancroftian infection from Brugian infection based on a newly identified gene from the W. bancrofti genome, abundant larval transcript-2 (alt-2), which is abundantly expressed. The difference in PCR product sizes generated from the presence or absence of evolutionarily altered tandem repeats in alt-2 intron-3 differentiated W. bancrofti from B. malayi. The analysis was performed on the genomic DNA of microfilariae from a number of patient blood samples or microfilariae positive slides from different Indian geographical regions. The assay gave consistent results, differentiating the two filarial parasite species accurately. This alt-2 intron-3 based PCR assay can be a potential tool for the diagnosis and differentiation of co-infections by lymphatic filarial parasites.
基于聚合酶链反应(PCR)的方法是监测和评估全球消灭淋巴丝虫病规划的有前途的工具。目前可用的 PCR 方法不能通过单个 PCR 区分班氏丝虫或马来丝虫的 DNA,因此比较繁琐。因此,我们设计了一种基于从班氏丝虫基因组中新鉴定的 abundantly larval transcript-2(alt-2)基因的一步法 PCR 策略,该基因大量表达。alt-2 内含子-3 中存在或不存在进化改变的串联重复序列产生的 PCR 产物大小的差异可区分班氏丝虫和马来丝虫。对来自不同印度地理区域的一些患者血液样本或微丝蚴阳性载玻片的微丝蚴基因组 DNA 进行了分析。该检测方法给出了一致的结果,可准确区分两种丝虫寄生虫。这种基于 alt-2 内含子-3 的 PCR 检测方法可能是用于诊断和区分淋巴丝虫寄生虫合并感染的潜在工具。