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ZusammenfassungIn einem Jungsauenerzeugerbetrieb in Niederösterreich traten über mehrere Jahre hinweg gehäuft Atemwegserkrankungen bei Jungsauen aus Eigenremontierung nach Einstallung in die Altsauenherde auf. Im Herbst 2019 wurden zudem Fruchtbarkeitsstörungen in Form von Spätaborten und Umrauschen beobachtet. Bei der Untersuchung von Nasentupfern mittels PCR auf Influenza-A-Virus (IAV) konnte bei 3 Jungsauen mit respiratorischer Symptomatik und Fieber der IAV-Subtyp H1avN1 nachgewiesen werden. Die Untersuchung der Serumproben dieser Tiere an 2 Zeitpunkten im Abstand von 3 Wochen ergab jedoch keinen Nachweis von Antikörpern im Hämagglutinationshemmtest (HAH), der standardmäßig im Labor verwendet wurde. Auch bei der Untersuchung von Sauen weiterer Altersgruppen waren keine eindeutigen Antikörpertiter gegenüber H1avN1 detektierbar. Nach Erweiterung des diagnostischen Panels des HAH um 7 H1avN1-Testantigene konnte eine Serokonversion um bis zu 3 Titerstufen bei den PCR-positiven Sauen gegenüber 2 verschiedenen H1avN1-Isolaten gemessen werden. Darüber hinaus ließen sich auch bei der Mehrzahl der restlichen untersuchten Altersgruppen hohe Antikörpertiter gegen diese beiden H1avN1-Teststämme nachweisen. Nach Anwendung des europaweit zugelassenen trivalenten Influenzaimpfstoffs konnte das klinische Erscheinungsbild in der Herde deutlich verbessert werden. Der Fallbericht verdeutlicht, dass für eine zielgerichtete Influenzadiagnostik der direkte und der indirekte Erregernachweis kombiniert verwendet werden sollten. Zudem wurde gezeigt, dass die kontinuierliche Anpassung von Testantigenen an die im Feld zirkulierenden Isolate überaus entscheidend für die Aussagekraft des HAH wäre.

Swine influenza A viruses (swIAVs) can play a crucial role in the generation of new human pandemic viruses. In this study, in-depth passive surveillance comprising nearly 2,500 European swine holdings and more than 18,000 individual samples identified a year-round presence of up to four major swIAV lineages on more than 50% of farms surveilled. Phylogenetic analyses show that intensive reassortment with human pandemic A(H1N1)/2009 (H1pdm) virus produced an expanding and novel repertoire of at least 31 distinct swIAV genotypes and 12 distinct hemagglutinin/neuraminidase combinations with largely unknown consequences for virulence and host tropism. Several viral isolates were resistant to the human antiviral MxA protein, a prerequisite for zoonotic transmission and stable introduction into human populations. A pronounced antigenic variation was noted in swIAV, and several H1pdm lineages antigenically distinct from current seasonal human H1pdm co-circulate in swine. Thus, European swine populations represent reservoirs for emerging IAV strains with zoonotic and, possibly, pre-pandemic potential.

BACKGROUNDHuman- or avian-to-swine transmissions have founded several autonomously circulating influenza A virus (IAV) lineages in swine populations that cause economically important respiratory disease. Little is known on other human influenza virus types, like B (IBV) and C (ICV) in European swine, and of the recently detected novel animal influenza virus type D (IDV).OBJECTIVESDevelopment of a cost-effective diagnostic tool for large-scale surveillance programmes targeting all four influenza virus types.METHODSAn influenza ABCD tetraplex real-time RT-PCR (RT-qPCR) was developed in the frame of this study. A selection of reference virus strains, and more than 4,000 porcine samples from a passive IAV surveillance programme in European swine with acute respiratory disease were examined.RESULTSTwo IBV, a single IDV but no ICV infections were identified by tetraplex RT-qPCR. IBV and IDV results were confirmed by conventional RT-PCR and partial sequence analysis.CONCLUSIONSThe tetraplex RT-qPCR proved fit for purpose as a sensitive, specific and high throughput tool to study influenza virus transmission at the human-animal interface. Complementing close-meshed active virological and serological surveillance is required to better understand the true incidence and prevalence of influenza virus type B, C and D infections in swine. This article is protected by copyright. All rights reserved.

Torque teno virus (TTV) is a non-enveloped virus with a circular, single-stranded DNA genome. TTV is currently classified in the unassigned genus Anellovirus, and distinct TTVs of tentative species-status infect a wide range of vertebrates. In domestic pigs and wild boars, porcine TTV occurs in two genogroups, TTV1 and TTV2, which are currently detected using only conventional PCR assays. To allow high-throughput testing, the present study describes development of a multiplex real-time (rt)-PCR assay for efficient simultaneous detection of TTV1 and TTV2. To demonstrate usefulness of this rt-PCR assay for large-scale testing, 203 serum samples from domestic pigs were screened for TTV infection. The detected rates of single TTV1, single TTV2, and double TTV1/TTV2 infections were 32, 17, and 32% and represent the first report on the occurrence of porcine TTV in Germany. In addition, 100 wild boar lung samples were tested that confirmed high prevalences of TTV infection. Moreover, establishment of genogroup-specific rt-PCR standards allowed the determination of mean viral genomic loads in sera from TTV-infected swine to about 10(4.5)/ml, respectively. To verify the specificity of the rt-PCR assay, conventional PCR assays that amplify genogroup-specific, size-distinguishable products from the TTV untranslated regions were designed. In total, 50 clones derived from 24 PCR products obtained from 19 TTV1 and TTV2 single- or double-infected animals were sequenced. Phylogenetic analyses of these sequences demonstrated the frequent occurrence of multiple infections with distinct porcine TTVs of the same genogroup. Moreover, two porcine TTV full-length sequences were established, one for each genogroup.

SummaryObjective: The aim of this field study was to explore the occurrence of and factors associated with the detection of swine influenza virus (SIV) by RTqPCR in weaner pigs and sows from herds with a history of respiratory or reproductive disorders. Material and methods: The sample set was based on nasal swabs from 823 sows (123 submissions) and 562 weaner pigs (80 submissions). Nasal swab samples were taken and submitted by 51 veterinary practices from all over Germany. Corresponding to the pig density most of the submissions ori ginated from the north-western part of Germany. The nasal swabs were used to detect SIV RNA by real-time RT-PCR (RTqPCR). Subtyping of SIV RNA by conventional RT-PCR and sequencing was attempted directly from clinical samples or from isolates when available. The herd characteristics, management and housing conditions of the pig herd as well as the course of the disease were collected by a telephone questionnaire with the herd attending veterinarian. Results: SIV was detected by RTqPCR in 53.8% of the submissions from weaner pigs with a history of respiratory disease. Moreover SIV was detected in 10.6% of the submissions from sows. The predominant endemic subtype found in nasal swabs from sows and weaner pigs was H1N1 (60.5%) whereas subtypes H1N2 (14.0%) and H3N2 (14.0%) were detected less frequently. In addition, human pandemic H1N1 virus or reassortants thereof were found in 11.5%. Conclusion and clinical relevance: The results underline the significance of a SIV infection in young pigs. A significant lower detection of SIV in weaner pigs was associated with the vaccination of piglets against porcine circovirus type 2 (PCV2), possibly indicating an interaction of SIV and PCV2. Most of the positive samples from sows originated from gilts, whereas only two originated from sows. An association between reproductive disorders and the detection of SIV could not be confirmed.

Samples were collected from 203 wild boars (Sus scrofa) hunted in Baden-Wurtemburg, Germany from November-January 2008 and 2009. Samples from the lung and tonsil were analyzed by quantitative polymerase chain reaction (qPCR) for porcine reproductive and respiratory syndrome virus (PRRSV) type 1 (European type) and type 2 (American type). A qPCR to detect porcine circovirus type 2 (PCV2)-specific genome was performed on tissue homogenates including lung, tonsils, and inguinal lymph nodes. Serum samples were tested for antibodies against PRRSV and PCV2 by enzyme-linked immunosorbent assay (ELISA). No PRRSV was detected in any of the 203 samples and one sample had detectable antibodies against PRRSV. We detected PCV2 in organ materials from 103 wild boars with a prevalence of 50.7%. The number of wild boars positive for PCV2 by PCR varied according to the population density of wild boars among woodlands. More positive samples were detected in woodlands with a high density of wild boars. We found no correlation between the number of PCV2-positive wild boars and the density of domestic pigs in the surrounding area. The number of wild boars positive for antibodies against PCV2 by the INGEZIM Circovirus IgG/IgM test kit was low (53 sera positive for IgG- and three sera positive for IgM-antibodies) in comparison to the higher positive results from the INGEZIM CIRCO IgG test kit (102 positive and 12 inconclusive results).

Pulmonary dysfunction was evaluated in pigs infected with porcine reproductive and respiratory syndrome virus (PRRSV, isolate VR-2332) and compared to clinical and pathological findings. Infected pigs developed fever, reduced appetite, respiratory distress and dullness at 9 days post-inoculation (dpi). Non-invasive pulmonary function tests using impulse oscillometry and rebreathing of test gases (He, CO) revealed peripheral airway obstruction, reduced lung compliance and reduced lung CO-transfer factor. PRRSV-induced pulmonary dysfunction was most marked at 9-18 dpi and was accompanied by a significantly increased respiratory rate and decreased tidal volume. Expiration was affected more than inspiration. On histopathological examination, multifocal areas of interstitial pneumonia (more severe and extensive at 10 dpi than 21 dpi) were identified as a possible structural basis for reduced lung compliance and gas exchange disturbances. (C) 2009 Elsevier Ltd. All rights reserved

Am 11. und 12. Mai 1999 fand das 16. Jenaer Symposium im Bundesinstitut fur gesundheitlichen Verbraucherschutz und Veterinarmedizin (BgW), Fachbereich 4 „Bakterielle Tierseuchen und Bekampfung von Zoonosen“ in Jena statt. Im Mittelpunkt der Tagung standen die Themenkomplexe „Respiratorische Erkrankungen und Zoonosen der Schweine“.