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  1. KHOA H C CÔNG NGH PH JNG TH C LÂY TRUY N C
  2. KHOA H C CÔNG NGH granosa) và hàu cLa sông (Crassostrea rivularis) 1.660 ± 593,8 bào tL/cá th3 $ %c b. trí ng9u nhiên 20 s ch b8nh $ %c thu tX nh?ng vùng nuôi không b cá th3/thùng x.p (th3 tích n #c là 10 L/thùng, kích b8nh Perkinosis t i B c Liêu. Nhóm nghêu b8nh th #c 30 x 25 x 25 cm) C nhi8t $) là 28 - 300°C, $) $ %c thu tX huy8n C^n GiU, thành ph. H@ Chí Minh mBn 25‰. MŠi nghi8m thbc $ %c lBp l i 3 l^n. MŠi n i nghêu $ %c báo cáo có tP l8 nhi m Perkinsus $ n v thí nghi8m $ %c b. trí 20 cá th3 nghêu. Cá th3 cao. o kích th #c và cân kh.i l %ng tXng cá th3 nghêu ch
  3. KHOA H C CÔNG NGH nhi m chéo và gây ch
  4. KHOA H C CÔNG NGH B6ng 2. C Ung $) nhi m Perkinsus olseni khi $i u tr bwng Desferrioxamine ThUi gian C Ung $) nhi m (bào tL/cá th3) $i u tr (ngày) 10 mg/L 15 mg/L 30 mg/L .i chbng 1 1.688 ± 128 2.033 ± 51 2.031 ± 34 1.613 ± 220 2 1.858 ± 139 1.800 ± 95 1.653 ± 114 1.687 ± 150 3 1.713 ± 97 1.612 ± 91 1.840 ± 63 1.760 ± 126 4 1.379 ± 150 1.677 ± 78 1.840 ± 129 1.627 ± 282 5 1.475 ± 62 1.400 ± 65 1.550 ± 318 1.693 ± 165 6 1.519 ± 110 1.483 ± 46 1.325 ± 86 1.762 ± 199 Ghi chú: S. li8u di n gi6i giá tr trung bình ± sai s. chumn Tuy thUi gian $i u tr trong thí nghi8m ng n (6 phát tri3n. P. marinus có th3 tránh $ %c oxy hóa gây ngày) nh ng b #c $^u crng $ã cho th5y $ %c hi8u 6nh h Cng $
  5. KHOA H C CÔNG NGH 4. Elandalloussi, L. M., Leite, R. B., Rodrigues, P. 10. OIE, 2012. Manual of Diagnostic Tests for M., Afonso, R., Nunes, P. A. & Cancela, M. L., 2005a. Aquatic Animals. Effect of antiprotozoal drugs on the proliferation of 11. Park, K. I. & Choi, K. S., 2001. Spatial the bivalve parasite Perkinsus olseni. Aquaculture, distribution of the protozoan parasite Perkinsus sp. 243(1-4), 9-17. found in the Manila clams, Ruditapes philippinarum, 5. Ford, S. E., Zhe, Xu & Debrosse, G., 2001. Use in Korea. Aquaculture, 203, 9-22. of particle filtration and UV irradiation to prevent 12. Patricia, da S. M., Carolina, P. C., Jaíse, de A. infection by Haplosporidium nelsoni (MSX) and P. B., Fernando, R. Q. & Alexandre, A. W., 2016. Perkinsus marinus (Dermo) in hatchery-reared Epizootiology of Perkinsus sp. in Crassostrea gasar larval and juvenile oysters. Aquaculture, 194, 37-49. oysters in polyculture with shrimps in northeastern 6. Gauthier, J. D. & Vasta, G. R., 1994. Inhibition Brazil. Brazilian Journal of Veterinary Parasitology, of in vitro replication of the oyster parasite Perkinsus 25, 37-45. marinus by the natural iron chelators transferrin, 13. Ray, S. M., 1952. A culture technique for the lactoferrin, and desferrioxamine. Dev. Comp. diagnosis of infections with Dermocystidium Immunol. 18(4), 277-286. marinum, Mackin, Owen and Collier, in oysters. 7. Goggin, C. L., Sewell, K. B. & Lester, R. J. G., Science, 116, 360-361. 1989. Cross-infection experiments with Australian 14. Ray, S. M., 1954. Biological studies of Perkinsus species. Diseases of Aquatic Organisms, 7, Dermocystidium marinus, a fungus parasite of 55-59. oysters. Rice University, Houston, TX. 8. La Peyre, M. K., Nickens, A. D., Volety, A. K., 15. Smolowitz, R., 2013. A Review of Current Tolley, G. S. & La Peyer, J. F., 2003. Environmental State of Knowledge Concerning Perkinsus marinus. significance of freshets in reducing Perkinsus Effects on Crassostrea virginica (Gmelin) (the marinus infection in eastern oysters Crassostrea Eastern Oyster). Veterinary Pathology, 50(3), 404- virginica: potential management applications. Marine 411. Ecology Progress Series 248, 165-176. 16. Tasumi, S. & Vasta, G. R., 2007. A galectin of 9. Mackin, J. G. & Hopkins, S. H., 1962. Studies unique domain organization from hemocytes of the on oyster mortality in relation to natural eastern oyster (Crassostrea virginica) is a receptor environments and to oil fields in Louisiana. for the protistan parasite Perkinsus marinus. J. University of Texas Institute of Marine Science. Immunol, 179, 3086-3098. TRANSMISSION OF Perkinsus olseni AND TREATMENT IN LABORATORY CONDITIONS Pham Quoc Hung, Ngo Thi Ngoc Thuy, Nguyen Thi Hong Nhung Summary The protozoan parasite Perkinsus olseni is a pathogen causing mass and severe mortalities in bivalve mollusc species in many countries in the world. In order to reduce the loss caused by this pathogen, it is vital to determine the preventive and therapeutic measures. The current study investigated the transmission of P. olseni among bivalve species and therapeutic efficiency of deferoxamine against perkinsus infection. The result indicated that P. olseni can be transmitted directly between individuals of Ben Tre clams and from infected Meretrix lyrata to cockle Anadara granosa and estuarine oyster Crassostrea rivularis. Using deferoxamine at doses of 15 and 30 mg/L was shown to reduce intensity of P. olseni infection. Keywords: Ben Tre clam, Deferoxamine, Perkinsus olseni, transmission. Ng Ui ph6n bi8n: TS. Võ Võ Th< Th< Drng Ngày nh;n nh;n bài: 26/5/2017 Ngày thông qua ph6n ph6n bi8n: bi8n: 29/6/2017 Ngày duy8t duy8t $ ng: 6/7/2017 94 N«ng nghiÖp vµ ph¸t triÓn n«ng th«n - KỲ 1 - TH¸NG 3/2018
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