Gou Hongchao, Bian Zhibiao, Cai Rujian, Jiang Zhiyong, Song Shuai, Li Yan, Chu Pinpin, Yang Dongxia, Zang Ying-An, Li Chunling
Institute of Animal Health, Guangdong Academy of Agricultural Sciences, Guangzhou, China.
Guangdong Provincial Key Laboratory of Livestock Disease Prevention, Guangzhou, China.
Front Vet Sci. 2020 Aug 4;7:407. doi: 10.3389/fvets.2020.00407. eCollection 2020.
In 2016, a novel porcine circovirus (PCV), PCV3, was identified in USA. Subsequently, it was proved to be also epidemic in China, Poland, and Korea. To analyze and control the epidemic situation of PCV3, it is necessary to establish accurate and high-throughput detection methods. In this study, the colorimetric isothermal multiple-self-matching-initiated amplification (IMSA) using cresol red was developed to detect PCV3 for the first time. The reaction can be easily performed by incubating the tube at 63°C for 60 min. By the addition of pH-sensitive indicator dye cresol red, the initial color of the reaction mixture is red. When PCV3 capsid gene DNA was positive in the sample, the color of the reaction mixture changed from red to yellow after the isothermal incubation at 63°C, while the negative control maintained the red color. The colorimetric IMSA displayed good specificity in detecting PCV3, PCV2, and PCV1 and 4 porcine DNA pathogens. Moreover, it has a low and repeatable detection limit of 10 copies, which is consistent with TaqMan-based qPCR, but 10 times more sensitive than PCR. In diagnosing 128 clinical specimens, it not only showed 100% agreement with qPCR but also detected 15 positive results more than PCR. The colorimetric IMSA we offered might be a good choice for PCV3 epidemiological investigation and point-of-care testing.
2016年,一种新型猪圆环病毒(PCV)——PCV3在美国被发现。随后,事实证明它在中国、波兰和韩国也有流行。为了分析和控制PCV3的疫情,有必要建立准确且高通量的检测方法。在本研究中,首次开发了使用甲酚红的比色等温多重自匹配引发扩增(IMSA)法来检测PCV3。该反应通过将试管在63°C孵育60分钟即可轻松完成。通过添加对pH敏感的指示染料甲酚红,反应混合物的初始颜色为红色。当样品中的PCV3衣壳基因DNA呈阳性时,在63°C等温孵育后,反应混合物的颜色从红色变为黄色,而阴性对照保持红色。比色IMSA在检测PCV3、PCV2以及PCV1和4种猪DNA病原体时表现出良好的特异性。此外,它具有低至10个拷贝的可重复检测限,这与基于TaqMan的定量PCR一致,但比PCR灵敏10倍。在诊断128份临床标本时,它不仅与定量PCR的结果100%一致,而且比PCR多检测出15个阳性结果。我们提供的比色IMSA可能是PCV3流行病学调查和即时检测的一个不错选择。