2014
DOI: 10.1186/1297-9716-45-12
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Vaccination of sows against type 2 Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) before artificial insemination protects against type 2 PRRSV challenge but does not protect against type 1 PRRSV challenge in late gestation

Abstract: The objective of the present study was to determine the effects of the commercially available type 2 Porcine Reproductive and Respiratory Syndrome Virus (PRRSV)-based modified live vaccine against type 1 and type 2 PRRSV challenge in pregnant sows. Half of the sows in the study were vaccinated with a type 2 PRRSV-based vaccine 4 weeks prior to artificial insemination while the other half remained non-vaccinated. Sows were then challenged intranasally with type 1 or type 2 PRRSV at 93 days of gestation. The sow… Show more

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Cited by 30 publications
(37 citation statements)
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“…In contrast, vaccination with the PRRSV-2 vaccine had limited effect on viremia following challenge with PRRSV-1 which also is in accordance with the outcome of most of the previous comparable studies with this vaccine [5,26,34].…”
Section: Discussionsupporting
confidence: 88%
“…In contrast, vaccination with the PRRSV-2 vaccine had limited effect on viremia following challenge with PRRSV-1 which also is in accordance with the outcome of most of the previous comparable studies with this vaccine [5,26,34].…”
Section: Discussionsupporting
confidence: 88%
“…PRRSV is classified into 2 major types: type 1 and type 2. There is very limited cross-protection between type 1 and type 2 PRRSV strains (17,18,70). Genetically, type 1 and type 2 PRRSVs share ϳ65% sequence identity (20,21).…”
Section: Discussionmentioning
confidence: 99%
“…Current PRRS MLV vaccines confer excellent protection against a PRRSV strain that is genetically similar to the vaccine strain (14,15). However, the levels of protection against heterologous PRRSV strains are highly variable and are considered suboptimal in all cases (10,(14)(15)(16)(17)(18)(19).…”
mentioning
confidence: 99%
“…However, it should be kept in mind that: (1) Protective NAb titers in blood (i.e. 1:8-1:32) are hard to obtain with just one application of currently available PRRSV vaccines (Han et al, 2014;Roca et al, 2012;Trus et al, 2014;Zuckermann et al, 2007); (2) Most of NAb are specific for the vaccine strain (homologous), as significant titers of cross-neutralizing antibodies are rare (Vu et al, 2011;Zhou et al, 2012); and (3) The anamnestic induction of NAb observed after heterologous challenge in some previously sensitized (vaccinated or previously infected) animals indicates a good prognosis of broad heterologous protection, but the anamnestic NAb response only seems to occur when a certain period of time has elapsed between primary sensitization and subsequent secondary heterologous challenge. The necessary length of time appears to be 2-3 months, if the challenge is one month or less, the anamnestic NAb response is not detected (Osorio et al, 1998;Scortti et al, 2006;Zuckermann et al, 2007).…”
Section: Role Of Neutralizing Antibodies In Protectionmentioning
confidence: 99%