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Occurrence ofClostridium perfringens vegetative cells and spores throughout an industrial production process of black soldier fly larvae (Hermetia illucens)

In: Journal of Insects as Food and Feed
Authors:
N. Van Looveren KU Leuven, Department of Microbial and Molecular Systems (M2S), Lab4Food, Geel Campus, 2440 Geel, Belgium.
KU Leuven, Leuven Food Science and Nutrition Research Centre (LFoRCe), Leuven, Belgium.

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https://orcid.org/0000-0001-9183-3494
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D. Vandeweyer KU Leuven, Department of Microbial and Molecular Systems (M2S), Lab4Food, Geel Campus, 2440 Geel, Belgium.
KU Leuven, Leuven Food Science and Nutrition Research Centre (LFoRCe), Leuven, Belgium.

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J. van Schelt Bestico B.V., 2651 BE Berkel en Rodenrijs, the Netherlands.

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L. Van Campenhout KU Leuven, Department of Microbial and Molecular Systems (M2S), Lab4Food, Geel Campus, 2440 Geel, Belgium.
KU Leuven, Leuven Food Science and Nutrition Research Centre (LFoRCe), Leuven, Belgium.

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Open Access

The main use of black soldier fly larvae (Hermetia illucens) is currently as an animal feed ingredient. While the bacterial community of the larvae has been characterised repeatedly via sequencing, microbiological safety assessment based on culture-dependent techniques is still scarce. This study focused on the occurrence of the spore-forming foodborne pathogenClostridium perfringens during rearing and consecutive processing of the larvae, based on observations in a single rearing facility.C. perfringens vegetative cells and spores were determined, in addition to total viable counts, total aerobic spore counts and intrinsic parameters including pH, water activity and moisture content. All samples were obtained from an industrial production plant. In a preliminary experiment, substrate ingredients and dried larvae were analysed, but the larvae were produced with a previous batch of the substrate mixture. A second, more detailed, experiment was performed where all samples were collected sequentially from the same production run (substrate ingredients, substrate mixture, starting larvae, harvested larvae, residue, dried larvae and stored dried larvae). In the two experiments, (presumptive)C. perfringens, as determined on tryptose sulphite cycloserine agar, was found at low numbers in the ingredients and in the second experiment it was also found in the substrate mixture. Over the two experiments, totalC. perfringens counts (i.e. vegetative cells plus spores) ranged between 3.0±0.1 and <1.2±0.5 log cfu/g andC. perfringens spores ranged between 2.5±0.1 and <1.0±0.0 log cfu/g. Interestingly, vegetative cells and spores ofC. perfringens were below the detection limit in all larvae samples. Therefore, it appears that at this production site and based on the samples investigated, the pathogen did not colonise the larvae. However, these results indicate that insect producers should monitor this pathogen among others, and install good hygiene practices to avoid contamination.

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