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Article

Lack of Acute Toxicity and Mutagenicity from Recombinant Epinephelus lanceolatus Piscidin Expressed in Pichia pastoris

1
Division of Applied Toxicology, Taiwan Agricultural Chemicals and Toxic Substances Research Institute, Council of Agriculture, Taichung City 41358, Taiwan
2
Department and Graduate Institute of Aquaculture, National Kaohsiung University of Science and Technology, Kaohsiung 811, Taiwan
3
Anbil Dharmalingam Agricultural College and Research Institute, Tamil Nadu Agricultural University, Tiruchchirapalli, Tamil Nadu 620027, India
4
Marine Research Station, Institute of Cellular and Organismic Biology, Academia Sinica, 23-10 Dahuen Road, Jiaushi, Ilan 262, Taiwan
5
The iEGG and Animal Biotechnology Center, National Chung Hsing University, Taichung 402, Taiwan
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Mar. Drugs 2020, 18(4), 206; https://doi.org/10.3390/md18040206
Submission received: 16 March 2020 / Revised: 4 April 2020 / Accepted: 8 April 2020 / Published: 11 April 2020

Abstract

The antimicrobial peptide (AMP) piscidin was identified from Epinephelus lanceolatus and demonstrated to possess antimicrobial and immune-related functions. Supplementation of feed with recombinant Epinephelus lanceolatus piscidin (rEP)-expressing yeast pellets may minimize the excessive use of antibiotics and control pathogens in aquaculture or animal husbandry. However, before implementing rEP as a supplement, it is necessary to understand whether it harbors any toxicity. Since toxicological information on the topic is scarce, the present investigation was carried out to test whether rEP exhibits allergenic and/or toxic effects. In an oral acute toxicity test (OECD 425), Sprague Dawley (SD) rats were administered rEP dissolved in reverse osmosis water, yielding an LD50 > 5000 mg/kg (no observed animal death). The compound was therefore classified as non-toxic by oral administration. In an acute respiratory toxicity test (OECD 403), heads and noses of SD rats were exposed to liquid aerosol for 4 h (the highest concentration that could be administered without causing any animal death), and a lethal concentration (LC50) > 0.88 mg/L was obtained. The mass medium aerodynamics diameter (MMAD) of rEP aerosol particles was 8.18 μm and mass medium aerodynamics diameter (GSD) was 3.04, which meant that 25.90% could enter the airway (<4 μm) of a rat, and 58.06% (<10 μm) could be inhaled by humans. An ocular irritation test (OECD 405) with rEP powder was performed on New Zealand White (NZW) rabbits. Signs of irritation included conjunctival swelling and diffuse flushing 1 h after administration. The signs were less apparent after 24 h and disappeared after 72 h. The classification assigned to the powder was mild eye irritation. Skin sensitization was performed for a local lymphoproliferative test (OECD 442B) using BALB/c mice, with the highest soluble concentration of the rEP considered to be 100% test substance; formulations were diluted to 50% and 25%, and bromodeoxyuridine (BrdU) incorporation was used to measure the degree of lymphocyte proliferation. The stimulation indexes (SIs) were 1.06 (100%), 0.44 (50%), and 0.77 (25%), all of which were less than the cutoff value for a positive sensitization result (1.6). Negative response was also seen in the bacterial reverse mutation test (OECD 471), and no chromosomal effects on Chinese hamster ovary (CHO)-K1 cells were observed (OECD 487). Based on these six toxicity tests, rEP showed neither acute toxic effects in experimental animals nor mutagenicity. Thus, rEP can be considered safe for use in subsequent research on its application as a feed additive for poultry, cattle, or aquatic animals.
Keywords: Epinephelus lanceolatus piscidin; antimicrobial peptide; recombinant piscidin; toxic effects; allergic effects; mutagenetic toxicity Epinephelus lanceolatus piscidin; antimicrobial peptide; recombinant piscidin; toxic effects; allergic effects; mutagenetic toxicity

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MDPI and ACS Style

Chen, H.-C.; Pan, C.-Y.; Rajanbabu, V.; Lee, Y.-Y.; Tsai, W.-R.; Chen, J.-Y. Lack of Acute Toxicity and Mutagenicity from Recombinant Epinephelus lanceolatus Piscidin Expressed in Pichia pastoris. Mar. Drugs 2020, 18, 206. https://doi.org/10.3390/md18040206

AMA Style

Chen H-C, Pan C-Y, Rajanbabu V, Lee Y-Y, Tsai W-R, Chen J-Y. Lack of Acute Toxicity and Mutagenicity from Recombinant Epinephelus lanceolatus Piscidin Expressed in Pichia pastoris. Marine Drugs. 2020; 18(4):206. https://doi.org/10.3390/md18040206

Chicago/Turabian Style

Chen, Hsiao-Ching, Chieh-Yu Pan, Venugopal Rajanbabu, Yen-Yun Lee, Wei-Ren Tsai, and Jyh-Yih Chen. 2020. "Lack of Acute Toxicity and Mutagenicity from Recombinant Epinephelus lanceolatus Piscidin Expressed in Pichia pastoris" Marine Drugs 18, no. 4: 206. https://doi.org/10.3390/md18040206

APA Style

Chen, H.-C., Pan, C.-Y., Rajanbabu, V., Lee, Y.-Y., Tsai, W.-R., & Chen, J.-Y. (2020). Lack of Acute Toxicity and Mutagenicity from Recombinant Epinephelus lanceolatus Piscidin Expressed in Pichia pastoris. Marine Drugs, 18(4), 206. https://doi.org/10.3390/md18040206

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