Virological and serological characterization of vaccinated and non-vaccinated piglet subpopulations coming from vaccinated and non-vaccinated sows.

The present study describes the virological and serological profiles of PCV2 vaccinated (V) and non-vaccinated (NV) piglet subpopulations coming from V and NV sows in a PCV2 subclinically infected farm. Four hundred seventy-six piglets born from V or NV sows were further subdivided in a total of four groups: NV sows-NV pigs (NV-NV), NV sows-V pigs (NV-V); V sows-NV pigs (V-NV) and V sows-V pigs (V-V). Seventy-five pigs were randomly selected at the beginning of the trial from each group and they were bled at 4, 8, 12, 16, 21 and 25 weeks of age. All animals included in the trial were weighed at 4 and 25 weeks of age and their average daily weight gain (ADWG) was calculated. Serum samples obtained at different time points were used to assess PCV2 infection (viremia) and the level of antibodies by means of immunoperoxidase monolayer assay (IPMA) against this pathogen. IPMA titers (classified in high, medium or low) and PCR results (positive or negative) were analyzed using a multiple correspondence and K-means cluster analysis. According to these tests, animals included in the study were classified into the following four clusters: (1) 93 piglets that were viremic mainly from 12 to 25 weeks of age and with PCV2 antibody titers increasing over time; (2) 75 piglets with late PCV2 infection and seroconversion (later than 16 weeks of age); (3) 26 piglets with high but decreasing PCV2 antibody titers and low percentages of PCV2 PCR positive serum samples; and (4) 105 piglets with medium and high IPMA titers throughout the trial and sporadic PCR positive samples. The defined subpopulations of piglets were observed in all experimental groups (NV-NV, NV-V, V-NV and V-V) although in variable percentages. Thus, animals from clusters 1 and 2 belonged mainly to the NV-NV and V-NV groups and animals from clusters 3 and 4 were distributed mainly into the NV-V and V-V groups. Finally, the ADWG of pigs belonging to clusters 3 and 4 was significantly higher (p=0.02) than that of pigs belonging to clusters 1 and 2. Within each cluster, no statistically significant differences were found in ADWG between treatment groups.

Humoral response and colostral antibody transfer following 'one-dose' pre-mating vaccination of sows against porcine circovirus type-2.

The objective of this study was to investigate the presence of porcine circovirus type 2 (PCV2) DNA and antibody to the virus in the serum and colostrum of sows vaccinated prior to mating and in their offspring. Seventy-seven sows were randomly distributed into vaccinated (V, n=36) and non-vaccinated (NV, n=41) groups. One week before mating, sows were given a PCV2 vaccine (V group) or PBS (NV group) IM. Blood samples were taken from the sows at fixed time-points and colostrum samples were taken at farrowing. Blood samples were also taken from the piglets of the sows at 4 weeks of age. The results indicated that vaccination prior to mating elicited a strong, homogeneous humoral response and, in consequence, more homogeneous colostral PCV2 antibody concentrations.

The blurred border between porcine circovirus type 2-systemic disease and porcine respiratory disease complex.

Porcine respiratory disease complex (PRDC) is the name used to describe a clinical presentation characterized by respiratory signs and poor growth in growing-finishing pigs. Porcine circovirus type 2 (PCV2) is one of the pathogens potentially involved in the presentation of this complex, although, it has been mainly linked to PCV2-systemic disease (PCV2-SD). However, some reports have suggested that PCV2 can cause respiratory lesions in the absence of systemic lymphoid damage; this apparently different condition has been referred as PCV2-lung disease (PCV2-LD). The present study analysed retrospectively the relation between PRDC and PCV2 infection from a pathological point of view. Of the 317 selected pigs suffering from PRDC and submitted for necropsy between 1998 and 2011, the most prevalent lesions were subacute interstitial pneumonia (27.7%) and the combination of subacute interstitial pneumonia plus catarrhal-purulent bronchopneumonia (28.4%). Two hundred and twenty-six pigs were positive for PCV2 by in situ hybridization (ISH); using immunohistochemical techniques, 77 were positive for porcine reproductive and respiratory syndrome virus and 3 for swine influenza virus. Among positive pigs for PCV2 ISH, 184 animals suffered from PCV2-SD. The rest of 42 PCV2 ISH positive pigs had no lymphoid lesions and low amount of viral nucleic acid in these tissues and, therefore, did not qualify for PCVD-SD; only 9 had concomitant PCV2 ISH positivity in the lung, also to a low amount. In conclusion, all PRDC-PCV2 ISH positive cases had evidence of viral systemic infection. These results suggest that PCV2-LD is probably a negligible condition and PCV2 mainly contributes to PRDC in relation to PCV2-SD occurrence.