많은 연구에 따르면 Tenebrio molitor은 유충 단계에서 플라스틱을 섭취할 수 있다고 보고되었다. 이 연구의 목적은 T. molitor 유충의 성장과 발달에 발포폴리스티렌 섭취가 미치는 영향을 조사하는 것이다. 밀기울을 섭취한 유충의 성장률은 발포폴리스티렌을 섭취한 유충의 성장률보다 더 좋았고(p < 0.001) 발포폴리스티렌을 섭취한 유 충의 번데기로 전환되는 기간은 밀기울을 섭취한 유충의 번데기로 전환되는 기간보다 더 빨랐다(p < 0.001). 하지만 두 처리구간 생존율은 유의미한 차이가 없었다(p = 0.786). 이 결과에 따르면 발포폴리스티렌을 섭취한 유충은 체중 감소와 짧은 발육기간이 특징이지만 생존하는 것에는 문제가 없었다. 따라서 우리는 T. molitor가 플라스틱 폐기물 의 지속 가능하고 친환경적인 제거를 위한 주요 자원이라는 결론을 내렸다.

거저리는 식품으로 사용되기 때문에 유충기가 오래 지속되면 더 좋다. 반면에 거저리의 개체수 유지를 위 해 성장을 가속화하기 위해서는 유충이 빨리 성충이 되면 더 좋다. 이 연구에서는 개체군 밀도가 거저리의 발달 시 간에 미치는 영향을 구명하였다. 이를 위해 상단 7 cm, 하단 5 cm, 높이 3 cm 크기의 용기를 사용했다. 거저리는 용기 당 1, 2, 5, 10, 20마리의 밀도로 용기에서 서식하였다. 용기에 밀기울 1 g을 넣고 거저리의 먹이 여부에 따라 라벨을 붙였다. 실험은 세 번 반복되었다. 모든 실험에서 개체군 밀도가 높을수록 유충에서 번데기로의 변환 시간이 짧았 지만 번데기에서 성충으로 변환되는 시간은 크게 다르지 않았다. 또한 먹이가 있는 그룹에서 번데기로의 변환 시간 이 단축되었지만, 성충으로 변환되는 시간에는 차이가 없었다. 이 연구 결과는 유충기를 연장하기 위해 더 낮은 밀 도가 필요하고 더 빠른 속도로 성충이 필요하다면 밀도가 더 높아야 한다는 것을 보여주었다. 결론적으로 거저리의 발달 시간은 개체수 밀도에 의해 제어할 수 있을 것이다.

Tenebrio molitor(T. molitor) is gaining attention as a sustainable food source with high nutrient content. Understanding their immune system, paricularly the role of Tak1 in the Imd pathway, is essential for mass breeding. This study investigates TmTak1 function in T. molitor. we investigated the immune function of TmTak1, followed by systemic infection using E. coli, S. aureus, and C. albicans. As a result, Silencing TmTak1 significantly affects expression levels of AMPs in the whole body, Fat bodies, and Integuments. These results showed lower expression levels of AMP compared to the control group during E.coli injection.

Tumor necrosis factor receptor-associated factor (TRAF) is known to regulate antimicrobial peptides (AMPs) production in mammals. Here, to understand the immunological function of TmTRAF against microbial challenge, the induction patterns of TmTRAF against microbial infection was investigated by qRT-PCR in the whole-body and tissue of young larvae. In addition, the effects of TmTRAF RNAi on larval mortality and expression of 15 AMP genes in response to microbial infection were investigated. Our studies may help to understand the basic role of AMP production.

In insects, the glutathione S-transferase is initiated in both the detoxification process and the protection of cellular membranes against oxidative damage. In this study, we identified the open reading frame (ORF) sequence of GST-iso1 and 2 from Tenebrio molitor (TmGST-iso1 and 2). To investigate the expression patterrns of TmGST-iso1 and 2 in response to herbicide, 0.06, 0.6, and 6 ㎍/㎕ of butachlor (FarmHannong, Seoul, South Korea) was challenged into T. molitor larvae, resulting that the TmGST-iso1 were highly induced at 3 and 24 h-post injection. Whereas, the highest expression of TmGST-iso2 was detected at 24 h after treatment. This study may contribute to basic information about the detoxifying activities of T. molitor.

Pelle, a serine/threonine kinase, is an intracellular component of the Toll pathway and is involved in antimicrobial peptides (AMPs) production due to pathogenic infection. It is known that the Pelle phosphorylates Cactus and activates the NF-κB signaling pathway in Drosophila, but it is not studied in Tenebrio molitor. In this study we investigated the tissue-specific expression patterns of the Pelle following pathogenic infection at 3, 6, 9, 12, and 24 hours. Additionally, larval mortality and AMP expression against microbial injection were investigated in dsPelle-treated T. molitor larvae. Our results may help to understand the antimicrobial function of TmPelle.

It is well known that the JNK pathway regulates AMP production against pathogenic infection in both vertebrates and invertebrates. Tenebrio molitor hep (Tmhep) is an homolog of MAP kinase kinase in mammals. Here, we investigate the immunological function of Tmhep in responses in microbial infection using RNA interference technology. The results showed that silencing of Tmhep increased the larval mortality against microbial challenge, as well as reduced AMP production compared to the control group (dsEGFP-treated group). Conclusively, Tmhep plays an critical role in antimicrobial defense in T. molitor larvae.

We introduce a method for preserving yellow mealwom (Tenebrio molitor) larvae for an extended period and show that a high percentage of larvae can survive in good health under low-temperature storage conditions combined with specific diapause termination conditions. When storing larvae for 140 days, the storage temperature can be varied based on our goals, giving us control over yellow mealworm production to meet specific demands. To produce adult beetles, storing larvae at 15 ℃ with wheat bran and ending diapause at 30 ℃ resulted in 90% pupation rate, with 60% becoming adults in 21 days. If our aim is larvae production, storing them at 10–12 ℃ with wheat bran and ending diapause at 25–30 ℃ allows the larvae to reach a suitable weight for processing. This approach ensures long-term storage of yellow mealworm larvae and provides a practical way to control their development, allowing efficient mass production tailored to market demands.