Persistence of Penaeus stylirostris densovirus delays mortality caused by white spot syndrome virus infection in black tiger shrimp (Penaeus monodon)

被引:14
作者
Molthathong, Sudkhate [1 ,2 ]
Jitrakorn, Sarocha [2 ,3 ]
Joyjinda, Yutthana [2 ]
Boonchird, Chuenchit [1 ]
Witchayachamnarnkul, Boonsirm [2 ,4 ]
Pongtippatee, Pattira [5 ]
Flegel, Timothy [1 ,2 ,3 ]
Saksmerprome, Vanvimon [2 ,3 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Biotechnol, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Sci, Centex Shrimp, Bangkok 10400, Thailand
[3] NSTDA, Natl Ctr Genet Engn & Biotechnol BIOTEC, Pathum Thani 12120, Thailand
[4] Shrimp Genet Improvement Ctr, Surat Thani, Thailand
[5] Aquat Anim Biotechnol Res Ctr, Surat Thani 84100, Thailand
关键词
PstDNV; IHHNV; Shrimp; WSSV; Real-time PCR; Multiplex PCR; HEMATOPOIETIC NECROSIS VIRUS; POLYMERASE-CHAIN-REACTION; GENOME; SEQUENCES; IHHNV;
D O I
10.1186/1746-6148-9-33
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Persistent infection of Penaeus stylirostris densovirus (PstDNV) (also called IHHNV) and its noninfectious inserts in the black tiger shrimp, Penaeus monodon (P. monodon) genome are commonly found without apparent disease. Here, we introduced the method of multiplex PCR in order to differentiate shrimp with viral inserts from ones with the infectious virus. The method allowed us to study the effect of pre-infection of IHHNV, in comparison to IHHNV inserts, on WSSV resistance in P. monodon. Results: A multiplex PCR system was developed to amplify the entire IHHNV genome, ensuring the accurate diagnosis. Field samples containing IHHNV DNA templates as low as 20 pg or equivalent 150 viral copies can be detected by this method. By challenging the two groups of diagnosed shrimp with WSSV, we found that shrimp with IHHNV infection and those with viral inserts responded to WSSV differently. Considering cumulative mortality, average time to death of shrimp in IHHNV-infected group (day 14) was significantly delayed relative to that (day 10) of IHHNV-inserted group. Real-time PCR analysis of WSSV copy number indicated the lower amount of WSSV in the IHHNV-infected group than the virus-inserted group. The ratio of IHHNV: WSSV copy number in all determined IHHNV-infected samples ranged from approximately 4 to 300-fold. Conclusion: The multiplex PCR assay developed herein proved optimal for convenient differentiation of shrimp specimens with real IHHNV infection and those with insert types. Diagnosed shrimp were also found to exhibit different WSSV tolerance. After exposed to WSSV, the naturally pre-infected IHHNV P. monodon were less susceptible to WSSV and, consequently, survived longer than the IHHNV-inserted shrimp.
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页数:7
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