Lecocq Antoine, Alencar Anna Luiza Farias, Lazov Christina M, Rajiuddin Sheikh M, Bøtner Anette, Belsham Graham J
Department of Plant and Environmental Sciences, University of Copenhagen, 1871 Frederiksberg C, Denmark.
Department of Veterinary and Animal Sciences, University of Copenhagen, 1870 Frederiksberg C, Denmark.
Pathogens. 2024 Nov 25;13(12):1038. doi: 10.3390/pathogens13121038.
Insect larvae production offers the potential for large-scale synthesis of high-quality protein that can be used as feed or food. However, currently, there are limitations on the source of substrates for the insect larvae to use. One concern is the potential survival of animal pathogens within insect larvae if their feed is contaminated. In this study, the survival of a very stable virus, porcine parvovirus (PPV), within mealworm () and black soldier fly (BSF) () larvae has been analyzed after oral ingestion of the virus. PPV genomic DNA could be readily detected by PCR in both species of larvae up until 9 days post ingestion (DPI), the end of the study period. Furthermore, infection of susceptible PK15 cells by PPV from homogenized mealworm larvae could be detected until at least 3 DPI, using an immunoperoxidase staining method and, up until 9 DPI, with a more sensitive real time PCR assay. Thus, PPV can remain infectious within mealworm larvae during their main growth phase through to their harvesting. However, it may be considered that PPV is exceptional in this respect since it displays unusual stability, e.g., to heat.
昆虫幼虫生产为大规模合成可作为饲料或食物的高质量蛋白质提供了潜力。然而,目前昆虫幼虫可用的底物来源存在限制。一个担忧是,如果昆虫幼虫的饲料受到污染,动物病原体可能在昆虫幼虫体内存活。在本研究中,分析了在口服感染一种非常稳定的病毒——猪细小病毒(PPV)后,黄粉虫幼虫和黑水虻幼虫体内该病毒的存活情况。直到摄入病毒后9天(dpi,研究期结束),通过PCR在两种幼虫中都能轻易检测到PPV基因组DNA。此外,使用免疫过氧化物酶染色法,直到至少3 dpi,以及使用更灵敏的实时PCR检测法直到9 dpi,均能检测到来自匀浆黄粉虫幼虫的PPV对易感PK15细胞的感染。因此,PPV在黄粉虫幼虫的主要生长阶段直至收获期间都可保持感染性。然而,鉴于PPV表现出不同寻常的稳定性,例如对热的稳定性,在这方面它可能被认为是例外情况。