{"refrec":{"BRefID":280879,"RR":"<b>Melena, J.; Bayot, B.; Betancourt, I.; Amano, Y.; Panchana, F.; Alday, V.; Calderon, J.; Stern, S.; Roch, P.; Bonami, J.R.</b> (2006). Pre-exposure to infectious hypodermal and haematopoietic necrosis virus or to inactivated white spot syndrome virus (WSSV) confers protection against WSSV in <i>Penaeus vannamei</i> (Boone) post-larvae. <i>J. Fish Dis. 29(10)</i>: 589-600. <a href=\"http://dx.doi.org/10.1111/j.1365-2761.2006.00739.x\" target=\"_blank\">dx.doi.org/10.1111/j.1365-2761.2006.00739.x</a>","BEntID":272898,"PublicFlag":1,"CheckedFlag":1,"wosflag":1,"vabbflag":1,"RefStringPartII":". <i>J. Fish Dis. 29(10)</i>: 589-600. <a href=\"https://dx.doi.org/10.1111/j.1365-2761.2006.00739.x\" target=\"_blank\">https://dx.doi.org/10.1111/j.1365-2761.2006.00739.x</a>","DocTypID":8,"DocType":"Journal article","MarineFlag":1,"FreshFlag":0,"BrackishFlag":0,"TerrestrialFlag":0,"Authorstring":"Melena, J.; Bayot, B.; Betancourt, I.; Amano, Y.; Panchana, F.; Alday, V.; Calderon, J.; Stern, S.; Roch, P.; Bonami, J.R.","OrigTitleTranslFlag":0,"Authorstringtrunc":"Melena, J. <i>et al.</i>","Englishabstract":"Larvae and post-larvae of <i>Penaeus vannamei</i> (Boone) were submitted to primary challenge with infectious hypodermal and haematopoietic necrosis virus (IHHNV) or formalin-inactivated white spot syndrome virus (WSSV). Survival rate and viral load were evaluated after secondary <i>per os</i> challenge with WSSV at post-larval stage 45 (PL45). Only shrimp treated with inactivated WSSV at PL35 or with IHHNV infection at nauplius 5, zoea 1 and PL22 were alive (4.7% and 4%, respectively) at 10 days post-infection (p.i.). Moreover, at 9 days p.i. there was 100% mortality in all remaining treatments, while there was 94% mortality in shrimp treated with inactivated WSSV at PL35 and 95% mortality in shrimp previously treated with IHHNV at N5, Z1 and PL22. Based on viral genome copy quantification by real-time PCR, surviving shrimp previously challenged with IHHNV at PL22 contained the lowest load of WSSV (0–1 × 10<sup>3</sup> copies <i>μ</i>g<sup>−1</sup> of DNA). In addition, surviving shrimp previously exposed to inactivated WSSV at PL35 also contained few WSSV (0–2 × 10<sup>3</sup> copies <i>μ</i>g<sup>−1</sup> of DNA). Consequently, pre-exposure to either IHHNV or inactivated WSSV resulted in slower WSSV replication and delayed mortality. 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