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首页> 外文期刊>International Journal of Food Microbiology >Revealing the microbiota of marketed edible insects through PCR-DGGE, metagenomic sequencing and real-time PCR
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Revealing the microbiota of marketed edible insects through PCR-DGGE, metagenomic sequencing and real-time PCR

机译:通过PCR-DGGE揭示营销食用昆虫的微生物群,偏见测序和实时PCR

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The present study aimed to identify the microbiota present in six species of processed edible insects produced in Thailand and marketed worldwide via the internet, namely, giant water bugs (Belostoma lutarium), black ants (Polyrhachis), winged termites (alates, Termitoidae), rhino beetles (Hyboschema contractum), mole crickets (Gryllotalpidae), and silkworm pupae (Bombyx mori). For each species, two samples of boiled, dried and salted insects were purchased. The microbial DNA was extracted from the insect samples and subjected to polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE), high-throughput sequencing and qualitative real-time PCR assays. The microbiota of the analyzed samples were widely characterized by the presence of spore-forming bacteria mainly represented by the genera Bacillus and Clostridium. Moreover, the genera Anaerobacillus, Paenibacillus, Geobacillus, Pseudomonas, Stenotrophomonas, Massilia, Delftia, Lactobacillus, Staphylococcus, Streptococcus, Vagococcus, and Vibrio were also detected. Real-time PCR allowed for ascertainment of the absence of Coxiella burnetii, Shiga toxin-producing E. coli (STEC), and Pseudomonas aeruginosa in all samples. The results of this study confirm the importance of combining different molecular techniques to characterize the biodiversity of complex ecosystems such as edible insects. The presence of potential human pathogens suggests the need for a careful application of good manufacturing practices during insect processing. This study provides further data that will be useful in risk analyses of edible insects as a novel food source.
机译:本研究旨在鉴定泰国生产的六种加工食用昆虫中的微生物群,并通过互联网销售全世界,即巨大水虫(Belostoma Lutarium),黑蚂蚁(Polyhachis),翼白蚁(Alates,Termitoidae),犀牛甲虫(Hyboschema收缩),鼹鼠蟋蟀(Gryllotalpidae)和蚕蛹(Bombyx Mori)。对于每种物种,购买了两种煮沸的,干燥和盐酸昆虫样品。从昆虫样品中提取微生物DNA,并进行聚合酶链反应变性梯度凝胶电泳(PCR-DGGE),高通量测序和定性实时PCR测定。分析的样品的微生物会被广泛的特征,其特征在于孢子形成细菌的存在,主要由Genera Bacillus和Clostridium表示。此外,还检测了属anaerobacillus,Paenibacillus,Geobacillus,假单胞菌,斯内特科米马拉斯,塞尔利亚,Delftia,乳酸杆菌,葡萄球菌,链球菌,凹陷和vibroco和vibro。实时PCR允许确定缺乏Coxiella Burnetii,Shiga毒素的生产大肠杆菌(STEC),以及所有样品中的假单胞菌铜绿假单胞菌。本研究的结果证实了与不同的分子技术相结合的重要性,以表征复杂生态系统等食用昆虫的生物多样性。潜在的人类病原体的存在表明需要在昆虫加工过程中仔细应用良好的制造实践。本研究提供了进一步的数据,该数据将是可食用昆虫作为新型食物来源的风险分析。

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