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Development of phage delivery by bioencapsulation of artemia nauplii with Edwardsiella tarda phage (ETP-1).
Nikapitiya, Chamilani; Dananjaya, S H S; Edirisinghe, Shan Lakmal; Chandrarathna, H P S U; Lee, Jehee; De Zoysa, Mahanama.
Afiliação
  • Nikapitiya C; College of Veterinary Medicine, Chungnam National University, Yuseong-gu, Daejeon, 34134, Republic of Korea.
  • Dananjaya SHS; College of Veterinary Medicine, Chungnam National University, Yuseong-gu, Daejeon, 34134, Republic of Korea.
  • Edirisinghe SL; College of Veterinary Medicine, Chungnam National University, Yuseong-gu, Daejeon, 34134, Republic of Korea.
  • Chandrarathna HPSU; College of Veterinary Medicine, Chungnam National University, Yuseong-gu, Daejeon, 34134, Republic of Korea.
  • Lee J; Fish Vaccine Research Center, Jeju National University, Jeju, Jeju Self-Governing Province, 63243, Republic of Korea. jehee@jejunu.ac.kr.
  • De Zoysa M; Department of Marine Life Sciences, Jeju National University, Jeju, Jeju Self-Governing Province, 63243, Republic of Korea. jehee@jejunu.ac.kr.
Braz J Microbiol ; 51(4): 2153-2162, 2020 Dec.
Article em En | MEDLINE | ID: mdl-32651888
ABSTRACT
This study proposed that phage-enriched artemia could be a useful tool for transferring phage into the cultured fish (larvae or adult) as a feed, and introduce mode of phage administration and its safety in concern of tissue adaptation for efficient phage therapy in aquatic animals. First, whether Edwardsiella tarda phage (ETP-1) could attach or ingest by the artemia and optimum time period for the ETP-1 enrichment with artemia were investigated. ETP-1 dispersion, abundance and persistency, and zebrafish immune transcriptional responses and histopathology were evaluated after feeding the fish with ETP-1-enriched artemia. Hatched artemia nauplii (36 h) were enriched with 1.90 × 1011 PFUmL-1 of ETP-1, and maintained at 25 °C. The highest enrichment level was obtained after 4 h (3.00 × 109 PFUmL-1), and artemia were alive and active similar to control for 8 h. ETP-1 disseminated dose dependently to all the tissues rapidly (12 h). However, when feeding discontinued, it drastically decreased at day 3 with high abundance and persistency in the spleen (1.02 × 103) followed by the kidney (4.00 × 101) and the gut (1 × 101 PFUmL-1) for highest ETP-1-enriched artemia dose. In contrast, during continuous delivery of ETP-1-enriched artemia, ETP-1 detected in all the tissues (at day 10 gut; 1.90 × 107, kidney; 3.33 × 106, spleen; 5.52 × 105, liver; 6.20 × 104 PFUmL-1mg-1 tissues). Though the phage abundance varied, results indicated that oral fed ETP-1-enriched artemia disperse to the neighboring organs, even the absence of host as phage carrier. Non-significant differences of immune transcriptional and histopathology analysis between ETP-1-enriched artemia fed and controls suggest that no adverse apparent immune stimulation in host occurred, and use of ETP-1 at 1011 PFUmL-1 was safe. With further supportive studies, live artemia-mediated phage delivery method could be used as a promising tool during phage therapy against pathogenic bacteria to control aquatic diseases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 3_ND Problema de saúde: 3_neglected_diseases / 3_zoonosis Assunto principal: Artemia / Edwardsiella tarda / Terapia por Fagos / Ração Animal Limite: Animals Idioma: En Revista: Braz J Microbiol Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 3_ND Problema de saúde: 3_neglected_diseases / 3_zoonosis Assunto principal: Artemia / Edwardsiella tarda / Terapia por Fagos / Ração Animal Limite: Animals Idioma: En Revista: Braz J Microbiol Ano de publicação: 2020 Tipo de documento: Article
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