Wen Shubo, She Lemuge, Dang Sheng, Liao Ao, Li Xiaorui, Zhang Shuai, Song Yang, Li Xiangyang, Zhai Jingbo
College of Animal Science and Technology, Inner Mongolia Minzu University, Tongliao, China.
Brucellosis Prevention and Treatment Technology Research Center, Tongliao, China.
Front Vet Sci. 2024 Sep 9;11:1440769. doi: 10.3389/fvets.2024.1440769. eCollection 2024.
Porcine Parvovirus (PPV) is a significant pathogen in the pig industry, with eight genotypes, including PPV7, identified since its emergence in 2016. Co-infections with viruses such as Porcine Circovirus 2 (PCV2) and Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) pose serious risks to swine health. Thus, there is an urgent need for rapid, sensitive, and specific detection methods suitable for use in field settings or laboratories with limited resources.
We developed a CRISPR/Cas12a-based assay combined with recombinase polymerase amplification (RPA) for the rapid detection of PPV7. Specific RPA primers and five CRISPR RNAs (crRNAs) were designed to target a highly conserved region within the NS1 gene of PPV7. Optimization of crRNA and single-stranded DNA (ssDNA) concentrations was performed to enhance the assay's performance.
CrRNA optimization identified crRNA-05 as the optimal candidate for Cas12a-based detection of PPV7, as all synthesized crRNAs demonstrated similar performance. The optimal crRNA concentration was determined to be 200 nM, yielding consistent results across tested concentrations. For ssDNA optimization, the strongest fluorescence signal was achieved with 500 nM of the FAM-BHQ ssDNA receptor. The assay showed a minimal detection limit of 100copies/μl for PPV7, confirmed through fluorescence and lateral flow detection methods. Specificity testing indicated that only PPV7 DNA samples returned positive results, confirming the assay's accuracy. In tests of 50 lung tissue samples from diseased pigs, the RPA-Cas12a assay identified 29 positive samples (58%), surpassing the 22 positive samples (44%) detected by conventional PCR. This highlights the RPA-Cas12a method's enhanced detection capability and its potential utility in clinical surveillance and management of PPV7 in swine populations.
The RPA-Cas12a assay effectively detects PPV7 in clinical samples, enhancing disease surveillance and control in pigs. Its adaptability to resource-limited settings significantly improves PPV7 management and prevention strategies, thereby supporting the overall health and development of the pig industry.
猪细小病毒(PPV)是养猪业中的一种重要病原体,自2016年出现以来已鉴定出包括PPV7在内的8种基因型。与猪圆环病毒2型(PCV2)和猪繁殖与呼吸综合征病毒(PRRSV)等病毒的共同感染对猪的健康构成严重风险。因此,迫切需要适用于现场环境或资源有限实验室的快速、灵敏且特异的检测方法。
我们开发了一种基于CRISPR/Cas12a的检测方法,并结合重组酶聚合酶扩增(RPA)用于快速检测PPV7。设计了特异性RPA引物和5种CRISPR RNA(crRNA)以靶向PPV7 NS1基因内的一个高度保守区域。对crRNA和单链DNA(ssDNA)浓度进行了优化以提高检测方法的性能。
crRNA优化确定crRNA-05是基于Cas12a检测PPV7的最佳候选者,因为所有合成的crRNA表现出相似的性能。确定最佳crRNA浓度为200 nM,在测试浓度范围内产生一致的结果。对于ssDNA优化,500 nM的FAM-BHQ ssDNA受体产生最强的荧光信号。该检测方法对PPV7的最低检测限为100拷贝/μl,通过荧光和侧流检测方法得到证实。特异性测试表明只有PPV7 DNA样本返回阳性结果,证实了该检测方法的准确性。在对50份病猪肺组织样本的检测中,RPA-Cas12a检测方法鉴定出29份阳性样本(58%),超过了传统PCR检测出的22份阳性样本(44%)。这突出了RPA-Cas12a方法增强的检测能力及其在猪群中PPV7临床监测和管理中的潜在效用。
RPA-Cas12a检测方法有效地检测临床样本中的PPV7,加强了猪病的监测和控制。其对资源有限环境的适应性显著改善了PPV7的管理和预防策略,从而支持养猪业的整体健康和发展。