A novel Respiratory Health Score (RHS) supports a role of acute lung damage and pig breed in the course of an Actinobacillus pleuropneumoniaeinfection
- Doris Hoeltig1,
- Isabel Hennig-Pauka1,
- Kerstin Thies1,
- Thomas Rehm2,
- Martin Beyerbach3,
- Katrin Strutzberg-Minder4,
- Gerald F Gerlach†2Email author,
- Karl-Heinz Waldmann†1 and
- FUGATO-consortium IRAS
© Hoeltig et al; licensee BioMed Central Ltd. 2009
Received: 23 October 2008
Accepted: 21 April 2009
Published: 21 April 2009
Bacterial lung infections are a major cause of economic losses in the pig industry; they are responsible for approximately 50% of the antibiotics used in pigs and, therefore, also present an increasing concern to consumer protection agencies. In response to this changing market we investigated the feasibility of an old approach aimed at the breeding selection of more resistant pigs. As a first step in this direction we applied a new respiratory health score system to study the susceptibility of four different pig breeding lines (German Landrace, Piétrain, Hampshire, Large White) towards the respiratory tract pathogen Actinobacillus (A.) pleuropneumoniae.
A controlled experimental aerosol infection with an A. pleuropneumoniae serotype 7 isolate was performed using 106 weaning pigs of defined breeding lines from the breeds German Landrace, Piétrain, Hamphire, and Large White. Pigs were clinically assessed on days 4 and 20 post infection following a novel scoring system, the Respiratory Health Score (RHS), which combines clinical, sonographic and radiographic examination results. The ranking on day 4 was significantly correlated with the ranking based on the pathomorphological Lung Lesion Score (LLS; Spearman Rank Correlation Coefficient of 0.86 [p < 0.0001]). Based on their RHS pigs were assigned to the different quartiles independent of the breeding line. The RHS-based rankings of pigs on day 4 and on day 20 were highly correlated (Spearman Rank Correlation Coefficient of 0.82 [p < 0.0001]) independent of the breeding line. Pigs of the Hampshire line were predominantly found in the lowest scoring quartile (47.6%) and absent in the highest scoring quartile. In contrast, pigs of the German Landrace and Piétrain breeding lines were predominantly found in the highest scoring quartile (32.3% and 35.7%, respectively).
These results demonstrate that the RHS obtained from live pigs shows a highly significant correlation to the lung lesion score considered as a "gold standard". The correlation of the ranking at days 4 and 20 post infection implies that the course of disease is highly dependent on the acute lung damage. The different severity of signs among the tested pig breeding lines clearly suggests a genetic difference in the susceptibility of pigs to A. pleuropneumoniae infection.
Bacterial respiratory diseases caused by Mycoplasma hyopneumoniae, Actinobacillus pleuropneumoniae, and Haemophilus parasuis are of major importance in the pig industry [1–3]. They cause severe economic losses due to premature deaths and reduced daily weight gains . Currently, productivity in infected herds is improved by antibiotic treatment and by vaccination regiments. However, vaccination efficacy is hampered by limited cross-serovar protection [5, 6], and treatment is impeded by the increasing occurrence of resistant strains . In addition, in recent years the interest of consumers in quality assurance along the pork production chain has greatly heightened. Thus, today there is a strongly increasing demand for pork obtained from healthy animals not subjected to treatment during the fattening period [8, 9].
In response to this changing market an old approach aimed at the breeding selection of more resistant pigs has gained renewed attention. In the past it could be shown that breed is an important factor influencing the baseline immune traits and, therefore, the response to various stressors or infectious challenges . For example, the susceptibility of pigs towards E. coli K88 which was identified to be of monogenic origin has been successfully suppressed by a targeted breeding approach [11, 12]. More recently, Reiner et al. showed that different breeds have distinct susceptibilities towards Pseudorabies virus  and Sarcocystis miescheriana ; QTL-mapping revealed that increased resistance to these pathogens is a complex trait. Also in the field of avian , ovine  and bovine diseases  natural resistance to different pathogens could be ascertained and used for the selection of a breeding population with increased resistance.
Concerning respiratory diseases of pigs a number of studies dealing with breed-dependent susceptibility towards viral infection (PCV-2, PRRSV) have been performed [18–22]. All of these studies provide strong evidence for genetic factors accountable for differences in susceptibility towards viral lung infections. In addition, a number of studies implied that there also is an influence of breed on the mortality of pigs suffering from bacterial lung infection [23–26].
The availability of increasing molecular information and new technologies such as i) a draft sequence of the porcine genome, ii) whole genome expression arrays, and iii) a porcine single nucleotide polymorphism (SNP) chip with 50.000 SNP now potentially facilitate the investigation of complex traits. As a first step in this direction we investigated the susceptibility of four different pig breeding lines (German Landrace, Piétrain, Hampshire, Large White) to infection with A. pleuropneumoniae. In order to minimize environmentally-induced variability, all pigs originated from the same herd and were subjected to experimental aerosol infection in a well-established A. pleuropneumoniae model [27–30]. All animals were phenotyped using an elaborate clinical investigation scheme including sonography and radiography before infection as well as on days 4 and 20 post infection , and a clinical assessment system, the Respiratory Health Score (RHS) was developed. Including all clinical investigation results this RHS facilitates an exact determination of the lung status in the living pig. Therefore, unlike the Lung Lesion Score (LLS), which is used as gold-standard for lung investigations until now , the RHS allows the comparison of the lung status at different time points after infection. The animals were consecutively ranked according to disease severity in acute (day 4) and chronic infection (day 20). Subsequently, the ranking of animals on both days and the number of animals from different breeding lines in the ranking quartiles were compared.
Development and validation of the Respiratory Health Score (RHS)
Upon infection the severity of clinical symptoms ranged from no symptoms to death. Clinical symptoms were typical for A. pleuropneumoniae infection with body temperatures up to 41.9°C, dyspnoea, coughing and apathy; likewise, ultrasonographic and radiographic results with comet tail artefacts, interruption of the pleural line, liver-like parenchyma texture, abscesses, bronchography, and increasing lung opacity were typical for porcine pleuropneumonia.
Comparative ranking of pigs on days 4 and 20 post infection
Susceptibility of different breeding lines upon infection with A. pleuropneumoniae
Range of RHS-points within the ranking quartiles at 4 and 20 days post infection
day 4 p. inf
(n = 96)
day 20 p. inf.
(n = 45)
0 – 2.1
0.21 – 3.33
2.11 – 10.7
3.34 – 18.8
10.71 – 27.5
18.81 – 34.91
27.51 – 95.61
34.92 – 99.12
RHS-based distribution of pigs from different breeding lines into ranking quartiles on day 4 post infection
German Landrace5) n = 27
Hampshire n = 21
Piétrain n = 28
Large White n = 16
RHS-based distribution of pigs from different breeding lines into ranking quartiles on on day 20 post infection
German Landrace5) n = 18
Hampshire n = 11
Piétrain n = 16
The intention of this study was to establish a combined quantitative scoring system to determine the lung status of diseased pigs avoiding the necessity of necropsy. All individual examination methods had been established previously, and the resulting individual scores (clinical, ultrasonographic and radiographic score) had been evaluated [31, 33–36]. However, none of these scores resulted in a ranking of pigs that correlated with the LLS considered as "gold standard". In the current work we examined the suitability of a combined score designated as Respiratory Health Score (RHS) including the clinical score and both ultrasonographic and radiographic examination of the lungs, as lung tissue alterations do not inevitably lead to clinical symptoms. These lung tissue alterations, however, can be visualized using imaging techniques with both radiographic and ultrasonographic examination methods having different limitations [37–42]. Also, neither ultrasonography nor radiography alone accurately depict the severity of lung tissue alterations. While affections of the pleura as well as sequestration of lung tissue at the lung surface could be clearly identified during the ultrasonographic examination, deep tissue alterations with no contact to the lung surface could only be detected radiographically. Using both methods, however, allows a comprehensive evaluation of the lung condition . For this reason the results of both methods are combined with the clinical score to result in a single value, the RHS. The RHS and the LLS are significantly correlated and, therefore, the RHS was considered appropriate as an alternative to the LLS. Since both imaging techniques can only be performed under anaesthesia the frequency of investigations is limited as immunosuppressive effects from anaesthesia cannot be excluded. In our experimental design we kept at least 14 days between two subsequent anaesthesias thereby minimizing possible detrimental effects. Despite these limitations the RHS, in our hands, is an excellent tool for all scientific investigations, where consecutive quantifications of the lung status during the course of disease in individual pigs are required.
The RHS system was applied to investigate the ranking of pigs in acute (day 4) and chronic infection (day 20 post infection). This comparison of RHS in the acute and chronic stages of disease was done to investigate the impact of the acute lung damage on the course of disease upon A. pleuropneumoniae infection. In the past, pigs with a low adaptive immune response have been compared to those with a high adaptive immune response ; the latter were then selected for breeding  hypothesising that these pigs might show an increase in general resistance to infectious diseases. However, since the degree of acute lung damage which is modulated by the innate immune system appears to have a strong impact on the course of disease the innate immune system might also play an important role in disease development.
Investigating possible differences among the breeding lines used in the study, various environmental factors with a potential influence on susceptibility such as origin of the pigs, age, and infectious dose were all standardized. Sex as another potential factor had been shown previously to not influence the course of disease . Other factors such as the social hierarchy within groups, differences in physical development between breeds , and the ability to adapt to new environments (e.g. unfamiliar management procedures or facilities, climate, herd size, or the contact to ubiquitous and contaminating microorganisms) were minimized by the experimental set-up in this study [45, 24, 46]. Thus, environmental and management conditions were highly standardized, and experiments were performed in groups containing a single breed as well as in groups containing different breeds.
The result of this study confirmed the low susceptibility of Hampshire pigs that had been described previously . Likewise, the previously described susceptibility within the breeds of Large White and German Landrace  was confirmed, and pigs of the Piétrain breeding line were found to be equally susceptible based on the RHS. The greater susceptibility of Large White pigs compared to the German Landrace pigs that was described after bacterial lung infections as well as after PCV-2 infections by other workers [23, 18] could not be observed. In contrast, the German Landrace pigs have to be considered as most susceptible as only pigs of this breeding line died or had to be euthanized due to severe clinical symptoms. This difference may be due to differences between local breeding lines or simply caused by the small number of Large White pigs in this study.
The genetic mechanisms responsible for the differences observed in susceptibility to A. pleuropneumoniae serotype 7 infection are still unknown; since the general mechanisms of pathogenicity are species-specific we expect similar results upon infection with other A. pleuropneumoniae serotypes. Future studies on this subject will be greatly facilitated by the finding that the acute lung damage appears to be decisive for the course of disease which allows termination of infection experiments on day 4 post infection without loss of information. Therefore, this work is considered to be an essential first step in the development of genetic markers that could be used for a breeding selection aimed at the increase of resistance to A. pleuropneumoniae infection. In addition, it might facilitate studies investigating genetic resistance of pigs to other bacterial respiratory tract pathogens.
In the course of these studies we demonstrated that the Respiratory Health Score (RHS) developed shows a highly significant correlation to the Lung Lesion Score (LLS) considered as a "gold standard". Therefore, the RHS allows the comparison of the lung status at different time points during infection in the same pig. The results of the lung status comparison between acute and chronic stage of pleuropneumonia strongly suggests that the acute lung damage is decisive for the course of disease. Furthermore, the different severity of symptoms among the tested breeding lines clearly implies that they have a highly distinct genetic susceptibility to A. pleuropneumoniae infection.
Animals, animal housing, and time course
A total of 106 pigs (40 German Landrace, 28 Pietrain, 22 Hampshire, 16 Large White) were infected. Three pigs (two German Landrace, one Hampshire) were not included into the study since the had contracted Oedema Disease. Due to severe clinical symptoms seven animals died or were sacrificed before day 4, and four animals were sacrificed after day 4 and before day 20 (all German Landrace). Thus, for 92 pigs (27 German Landrace, 28 Piétrain, 21 Hampshire, 16 Large White) both, a RHS and a LLS could be obtained. Of these, 47 pigs (9 German Landrace, 12 Piétrain, 10 Hampshire, 16 Large White) were randomly selected and sacrificed on day 4; the remaining 45 pigs (18 German Landrace, 16 Piétrain, 11 Hampshire) were sacrificed on day 20 post infection. Material from the same pigs was simultaneously used in a parallel study investigating expression levels of immune markers in relation to breeding line and the disease severity .
At the time of infection pigs were 6 to 7 weeks old and were tested negative for A. pleuropneumoniae using an ApxIIA  and an ApxIVA ELISA . In addition, all pigs tested negative for Mycoplasma hyopneumoniae and PRRS by antibody ELISA (HerdChek*, IDEXX Laboratories, Westbrook, Maine, USA), and Influenca-A-Virus by hemagglutination inhibition test using porcine H1N1, H1N2 and H3N2 strains. During the entire time (before and after infection) pigs were kept under standardized containment level 2 conditions with 8 m2 floor space per 10 pigs, with standardized climate and diet, and cared for in accordance with the principles outlined by the European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes (European Treaty Series, nos. 123 http://conventions.coe.int/treaty/EN/treaties/html/123.htm and 170 http://conventions.coe.int/treaty/EN/treaties/html/170.htm; approval number: 33-42502-05/941). In order to reduce the impact of stress on the examination results pigs were randomised into different groups at the age of four weeks and accustomed to handling over a one- to two-week period prior to aerosol infection. The examination period lasted four weeks, from seven days before until 20 days after infection. Radiography and sonography were done three times, namely on day 7 before and on days 4 and 20 after infection.
At the end of the experiment pigs were necropsised; the lung damage was quantified using the Lung Lesion Score (LLS) proposed by Hannan et al.  and specified in the European Pharmacopoeia for the testing of A. pleuropneumoniae vaccines (3 rd edn., EDQM, Council of Europe, Strassbourg, France). The LLS is determined after the removal of the lungs from the thorax in the course of necropsy. The lungs are palpated and areas of non-physiological consistence are recorded in a schematic map of the porcine lung. In this map the pulmonary lobes are subdivided into triangles (7 triangles for each, cranial and middle lobes, 19 triangles for caudal lobes, and 8 triangles for the Lobus accessories). In the LLS (maximum value of 35) each lobe contributes a maximum score of 5 (tissue damage in the entire lobe). To determine the LLS the damaged area is determined by counting the number of triangles indicating tissue damage and expressing it as a fraction of five for each lobe. The values for each of the seven lobes are added to result in the LLS.
Experimental infection and clinical investigation
Aerosol infection was performed using A. pleuropneumoniae serotype 7 strain AP76 as previously described [50, 51]; during infection approximately 1 × 105 bacteria were nebulised for five pigs resulting in an aerosol with 1 × 102 colony forming units (cfu) of A. pleuropneumoniae per litre aerosol.
Clinical signs were monitored daily and consisted of an assessment of general appearance (posture, behaviour, feed intake, temperature, vomiting) and respiratory tract (breathing noise, dyspnoea, respiratory frequency, coughing, pulsoxymetric oxygen saturation [Pulsoxymeter NPB-40, Fa. Nellcor Puritan Benett Inc., Boulder, U.S.A.] and cyanosis); pulsoxymetric oxygen saturation was measured at the lower side of the tail . Parameters with two specifications (vomiting) were scored with 0 or 4 points, parameters with three specifications (dyspnoe) with 0, 2, or 4 points, parameters with four specifications (breathing noise, coughing, feed intake) with 0, 1.33, 2,67, or 4 points, and the remaining parameters with five specifications with 0, 1, 2, 3, or 4 points . The points were added and divided by 11 to result in the daily clinical score resulting in a score of 0 for a healthy animal and a maximum score of 4 for a severely diseased animal; a dead animal was scored with 5 points. The clinical score on day 4 is the sum of the daily clinical score from days 1 to 4; the clinical score on day 20 is calculated accordingly .
Ultrasonographic and radiographic examinations of the lungs both were performed under anaesthesia with 15 mg/kg Ketamine i.m. (Ursotamin®, Fa. Serum-Werk-Bernburg AG, Bernburg, Germany) and 2 mg/kg i.m. Azaperon (Stresnil®, Fa. Janssen-Cilag GmbH, Baar, Switzerland). Ultrasonography of the lungs was performed with an 8 MHz linear scanner (LOGIQ™ Book XP, Fa. GE Medical Systems, Chalfont St. Giles, Great Britain) in lateral position. On either side of the chest each intercostal space was scanned in dorso-ventral direction. Right and left lung are each divided into 5 sections, and each section is sub-divided into the intercostal spaces . Comet-tail-artefacts, echogenicity, consolidations, and sequesters were analysed with a point range from 0 (physiological findings) to 8 (no unaltered lung tissue seen). The addition of the score points given for the observed alterations resulted in the sonographic score with a score of 200 being lethal .
Radiography was carried out in two views (latero-lateral and dorso-ventral; Convix Generator 360, Fa. Picker Int., Munich, Germany, 400 mAs, 110 kV, 1000 ms) using a shutter priority (Precimat, Fa. Picker Int.). In the radiographic score the lung was divided into eight sections. Bronchial, alveolar and interstitial patterns, cardiac and diaphragm silhouette and sequesters were analysed with a point range from 0 to 3. The addition of the score points given for the observed alterations resulted in the radiographic score with a score of 50 being lethal .
Development of a Respiratory Health Score (RHS)
For quantification of the examination results the Respiratory Health Score (RHS) was developed based on a combination of the clinical, sonographic and radiographic scores. The RHS is a score that indicates the degree of lung alteration in percent of the maximum alteration possible in a live animal. Briefly, individual scores are normalized by division with the score causing death in an animal, added, divided by three and multiplied by 100 in order to get a value in percent (Fig. 1). Therefore, the RHS has a possible range from 0 to 100%.
For statistical analyses of the data SAS® software (SAS Institute Inc., Cary, NC, USA) was used. Correlations of i) LLS and RHS and ii) RHS on days 4 and day 20 post infection were assessed by calculating the Spearman Rank Correlation Coefficient.
This research was supported by the Development Association for Biotechnology (FBF) and the German Ministry of Education and Research (BMBF) (FUGATO, IRAS FKZ 0313389 A-E).
other IRAS members are: Hannover Medical School, Helmholtz Centre for Infection Research Braunschweig, Max Planck Institute for Molecular Genetics, Otto-von-Guericke University Magdeburg, LIONEX GmbH Braunschweig, RZPD GmbH Berlin, and the contributing scientists (in alphabetical order) Benga L, Blöcker H, Danilowicz E, Drungowski M, Herwig R, Kahlisch D, Leeb T, Martinez R, Naim HY, Pabst R, Probst I, Radelof U, Rothkötter HJ, Singh M, Spallek R, Stanke F, Tümmler B, Valentin-Weigand P, Wagner F.
- Altrock Av: Occurrence of bacterial agents in lungs of pigs and evaluation of their resistance to antibiotics. Berl Munch Tierarztl Wschr. 1998, 111: 164-172.Google Scholar
- Ross RF: Mycoplasma disease. Disease of Swine. Edited by: Leman AD, Straw B, Glock R, Mengeling WL, D'Allaire S, Taylor DJ. Ames, Iowa State University Press; 1992:552-559. 7Google Scholar
- Sebunya TNK, Saunders JR: Haemophilus pleuropneumoniae infection in swine: a review. J Am Vet Med Assoc. 1983, 182: 1331-1337.PubMedGoogle Scholar
- Noyes EP, Feeney D, Pijoan C: Comparison of the effect of pneumonia detected during lifetime with pneumonia detected at slaughter on growth in swine. J Am Vet Med Assoc. 1990, 197: 1025-1029.PubMedGoogle Scholar
- Fenwick B, Henry S: Porcine pleuropneumonia. J Am Vet Med Assoc. 1994, 204: 1334-1340.PubMedGoogle Scholar
- Higgins R, Lariviere S, Mittal KR, Martineau GP, Rousseau P, Cameron J: Evaluation of a killed vaccine against porcine pleuropneumonia due to Haemophilus pleuropneumoniae. Can Vet J. 1985, 26: 86-89.PubMed CentralPubMedGoogle Scholar
- White DG, Zhao S, Simjee S, Wagner DD, McDermott PF: Antimicrobial resistance of foodborne pathogens. Microbes Infect. 2002, 4: 405-412. 10.1016/S1286-4579(02)01554-X.View ArticlePubMedGoogle Scholar
- Borowy N: Ist das Schwein gesund, freut sich der Verbraucher. Leibnitz Nordost. 2005, 1: 9-10.Google Scholar
- Van Oirschot JT: Vaccination in food animal populations. Vaccine. 1994, 12: 415-418. 10.1016/0264-410X(94)90117-1.View ArticlePubMedGoogle Scholar
- Sutherland MA, Rodriguez-Zas SL, Ellis M, Salak-Johnson JL: Breed and age affect baseline immune traits, cortisol and performance in growing pigs. J Anim Sci. 2005, 83: 2087-2095.PubMedGoogle Scholar
- Meijerink E, Fries R, Vögeli P, Masabandra J, Wigger G, Stricker C, Neuenschwander S, Bertschinger HU, Stranzinger G: Two alpha(1,2) fucosyltransferase genes on porcine chromosome 6q11 are closly linked to the blood group inhibitor S and Escherichia coli F18 receptor (ECF18R) loci. Mamm Genome. 1997, 8: 736-741. 10.1007/s003359900556.View ArticlePubMedGoogle Scholar
- Voegeli P, Meijerink E, Fries R, Neuenschwander S, Vorlander N, Stranzinger G, Bertschinger HU: [A molecular test for the detection of E. coli F18 receptors: a breakthrough in the struggle against edema disease and post-weaning diarrhea in swine]. Schweiz Arch Tierheilkd. 1997, 139 (11): 479-484.Google Scholar
- Reiner G, Melchinger E, Kramarowa M, Pfaff E, Büttner M, Saalmüller A, Geldermann H: Detection of quantitative trait loci for resistance/susceptibility to pseudorabies virus in swine. J Gen Virol. 2002, 83: 167-172.View ArticlePubMedGoogle Scholar
- Reiner G, Willems H, Berge T, Fischer R, Köhler F, Hepp S, Hertrampf B, Kliemt D, Daugschies A, Geldermann H, Mackenstedt U, Zahner H: Mapping of quantitative trait loci for resistance/susceptibility to Sarcocystis miescheriana in swine. Genomics. 2007, 89: 638-646. 10.1016/j.ygeno.2007.01.011.View ArticlePubMedGoogle Scholar
- Cole RK: Studies on genetic resistance to Marek's disease. Avian Dis. 1968, 12: 9-28. 10.2307/1588081.View ArticlePubMedGoogle Scholar
- Stear MJ, Wakelin D: Genetic resitance to parasitic infection. Rev sci tech Off Int Epiz. 1998, 17: 143-153.Google Scholar
- Heringstad B, Klemetsdal G, Ruane J: Selection for mastitis resitance in daity cattle: a review with focus on the situation in the Nordic countries. Livestock Prod Sci. 2000, 64: 95-106. 10.1016/S0301-6226(99)00128-1.View ArticleGoogle Scholar
- Opriessnig T, Fenaux M, Thomas P, Hoogland MJ, Rothschild MF, Meng XJ, Halbur PG: Evidence of breed-dependend differences in susceptibility to porcine circovirus type-2-associated disease and lesions. Vet Pathol. 2006, 43: 281-293. 10.1354/vp.43-3-281.View ArticlePubMedGoogle Scholar
- Vincent AL, Thacker BL, Halbur PG, Rothschild MF, Thacker EL: An investigation of susceptibility to porcine reproductive and respiratory syndrome virus between two genetically diverse commercial lines of pigs. J Anim Sci. 2006, 84: 49-57.PubMedGoogle Scholar
- Halbur P, Rothschild MF, Thacker B: Differences in susceptibility of Duroc, Hampshire and Meishan pigs to infection with high-virulence strain (VR2385) of porcine reproductive and respiratory syndrome virus (PRRSV). J Anim Breed Genet. 1998, 115: 181-189.View ArticleGoogle Scholar
- Petry DB, Holl JW, Weber JS, Doster AR, Osorio FA, Johnson RK: Biological response to porcine respiratory and reproductive syndrome virus in pigs of two genetic populations. J Anim Sci. 83: 1494-1502.Google Scholar
- Petry DB, Lunney J, Boyd P, Kuhar D, Blankenship E, Johnson RK: Differential immunity in pigs with high and low response to porcine reproductive and respiratory syndrome virus infection. J Anim Sci. 2007, 85: 2075-2092. 10.2527/jas.2006-721.View ArticlePubMedGoogle Scholar
- Jones JET: The incidence and nature of diseases causing death in pigs aged 2–7 month in a commercial herd. Br Vet J. 1968, 125: 492-505.Google Scholar
- Straw BE, Neubauer GD, Leman AD: Factors affecting mortality in finishing pigs. J Am Vet Med Assoc. 1983, 183: 452-455.PubMedGoogle Scholar
- Lundeheim N: Genetic analysis of respiratory diseases in pigs. Acta Agric Scand. 1979, 29 (3): 209-215.View ArticleGoogle Scholar
- Jorgensen B: Group-level effects of breed and sire on diseases and influence of diseases on performance of pigs in Danish test stations. Prev Vet Med. 1992, 14 (3–4): 281-292. 10.1016/0167-5877(92)90024-A.View ArticleGoogle Scholar
- Baltes N, Topitak W, Gerlach GF, Hennig-Pauka I, Hoffmann-Moujahid M, Ganter M, Rothkotter HJ: Actinobacillus pleuropneumoniae iron transport and urease activity: effects on bacterial virulence and host immune response. Infect Immun. 2001, 69: 472-478. 10.1128/IAI.69.1.472-478.2001.PubMed CentralView ArticlePubMedGoogle Scholar
- Baltes N, Hennig-Pauka I, Jacobsen I, Gruber AD, Gerlach GF: Identification of dimethyl sulfoxide reductase in Actinobacillus pleuropneumoniae and its role in infection. Infect Immun. 2003, 71: 6784-6792. 10.1128/IAI.71.12.6784-6792.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Baltes N, Tonpitak W, Hennig-Pauka I, Gruber AD, Gerlach GF: Actinobacillus pleuropneumoniae serotype 7 siderophore receptor FhuA is not required for virulence. FEMS Microbiol Lett. 2003, 220: 41-48. 10.1016/S0378-1097(03)00064-8.View ArticlePubMedGoogle Scholar
- Jacobsen I, Hennig-Pauka I, Baltes N, Trost M, Gerlach GF: Enzymes involved in anaerobic respiration appaer to play a role in Actinobacillus pleuropneumoniae virulence. Infect Immun. 2005, 73: 226-234. 10.1128/IAI.73.1.226-234.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Hoeltig D, Hennig-Pauka I, Thies K, Rehm T, Gerlach GF, Waldmann KH: Comparison of the diagnostic statement of clinical, radiographic and ultrasonographic results after an experimental infection with Actinobacillus pleuropneumoniae in pigs. Berl Munch Tierarztl Wochenschr. 2008, 121 (11/12): 422-431.Google Scholar
- Hannan PC, Bhogal BS, Fish JP: Tylosin tartrate and tiamutilin effects on experimental piglet pneumonia induced with pig lung homogenate containing mycoplasmas, bacteria and viruses. Res Vet Sci. 1982, 33: 76-88.PubMedGoogle Scholar
- Dudziak D: Klinische Verlaufskontrolle einer oralen Chlortetrazyklinbehandlung bei lungenkranken Schweinen mittels Röntgendiagnostik und Pulsoxymetrie. Dissertation, Tieraerztliche Hochschule Hannover Hannover. 1995, [http://elib.tiho-hannover.de/dissertations/95dudziak-d.pdf]Google Scholar
- Gierke Kv: Klinische Diagnostik von Lungenerkrankungen beim Schwein mit besonderer Berücksichtigung der Röntgenuntersuchung im Vergleich mit pathologisch-anatomischen Befunden. Dissertation, Tieraerztliche Hochschule Hannover. 1997, [http://elib.tiho-hannover.de/dissertations/97gierke-von-k.pdf]Google Scholar
- Heinritzi K, Beisl J: The application of sonography for swine. Dtsch Tierarztl Wschr. 1995, 102: 4-15.Google Scholar
- Schulze W, Schröder I, Arbeiter K: The respiratory rate of the pig. Dtsch Tierarztl Wschr. 1963, 22: 620-624.Google Scholar
- Farrow CS: Equine thoracic radiology. J Am Vet Med Assoc. 1981, 179: 611-615.Google Scholar
- Farrow CS: Radiography of the equine thorax: anatomy and technic. Vet Radiol. 1981, 22: 62-68. 10.1111/j.1740-8261.1981.tb01694.x.View ArticleGoogle Scholar
- Klein C: Sonographie der Lunge und Analyse der Atmungsmechanik mittels Impuls-Oszilloresistometrie beim lungengesunden und pneumoniekranken Ferkel und Läuferschwein. Dissertation. Universität Leipzig; 1999.Google Scholar
- Reef VB, Boy MG, Reid CF, Elser A: Comparison between diagnostic ultrasonography und radiography in evaluation of horses und cattle with thoracic disease: 56 cases (1984 – 1985). J Am Vet Med Assoc. 1991, 198: 2112-2117.PubMedGoogle Scholar
- Reinhold P, Rabeling B, Günther H, Schimmel D: Comparative evaluation of ultrasonography and lung function testing with the clinical signs and pathology of calves inoculated experimentally with Pasteurella multocida. Vet Rec. 2002, 150: 109-114.View ArticlePubMedGoogle Scholar
- Tobin E: Thoracic radiology part 1: the respiratory system, pleural space and mediastinum. Ir Vet J. 2004, 57: 598-604.Google Scholar
- Magnusson U, Bosse J, Mallard BA, Rosendal S, Wilkie BN: Antibody response to Actinobacillus pleuropneumoniae antigens after vaccination of pigs bred for high and low immune response. Vaccine. 1997, 15: 997-1000. 10.1016/S0264-410X(96)00294-0.View ArticlePubMedGoogle Scholar
- Magnusson U, Wilkie B, Mallard B, Rosendal S, Kennedy B: Mycoplasma hyorhinis infection of pigs bred for high and low immune response. Vet Immun Immunpathol. 1998, 1: 83-96. 10.1016/S0165-2427(97)00132-3.View ArticleGoogle Scholar
- Done SH: Environmental factors affecting the severity of pneumonia in pigs. Vet Rec. 1991, 128: 582-586.View ArticlePubMedGoogle Scholar
- Waldmann KH: Housing- and management-specific effects on the health of swine. Dtsch Tierarztl Wschr. 2003, 110: 328-330.Google Scholar
- Benga L, Hoeltig D, Rehm T, Rothkoetter HJ, Pabst R, Valentin-Weigand P: Expression levels of immune markers in Actinobacillus pleuropneumoniae infected pigs and their relation to breed and clinical symptoms. BMC Vet Res. 5: 13-10.1186/1746-6148-5-13.Google Scholar
- Leiner G, Franz B, Strutzberg K, Gerald GF: A novel enzyme-linked immunosorbent assay using the recombinant Actinobacillus pleuropneumoniae ApxII antigen for diagnosis of pleuropneumonia in pig herds. Clin Diagn Lab Immunol. 1999, 6: 630-632.PubMed CentralPubMedGoogle Scholar
- Dreyfuß A, Schaller A, Nivollet S, Segers RPAM, Kobisch M, Mieli L, Soerensen V, Hussy D, Miserez R, Zimmermann W, Inderbitzin F, Frey J: Use of recombinant ApxIV in serodiagnosis of Actinobacillus pleuropneumoniae infections, development and prevalidation of the Apx IV Elisa. Vet Microbiol. 2004, 99: 227-238. 10.1016/j.vetmic.2004.01.004.View ArticleGoogle Scholar
- Jacobsen MJ, Nielsen JP, Nielsen R: Comparison of virulence of different Actinobacillus pleuropneumoniae serotypes and biotypes using an aerosol infection model. Vet Microbiol. 1996, 49: 159-168. 10.1016/0378-1135(95)00184-0.View ArticlePubMedGoogle Scholar
- Maas A, Meens J, Baltes N, Hennig-Pauka I, Gerlach GF: Development of a DIVA subjunit vaccine against Actinobacillus pleuropneumoniae infection. Vaccine. 2006, 24: 7226-7237. 10.1016/j.vaccine.2006.06.047.View ArticlePubMedGoogle Scholar
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