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Herd specific risk factors for Mycoplasma hyopneumoniae infections in suckling pigs at the age of weaning

Heiko Nathues12, Henrike Woeste1, Stefanie Doehring1, Anna S Fahrion3, Marcus G Doherr3 and Elisabeth grosse Beilage1*

Author Affiliations

1 Field Station for Epidemiology, University of Veterinary Medicine Hannover, Foundation, Buescheler Street 9, Bakum D-49456, Germany

2 Veterinary Epidemiology, Economics and Public Health Group, Department of Production and Population Health, Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire, AL9 7TA, UK

3 Veterinary Public Health Institute, Department of Clinical Research - Veterinary Public Health, Vetsuisse Faculty, University of Bern, Schwarzenburgstrasse 155, Liebefeld (BE), CH-3097, Switzerland

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Acta Veterinaria Scandinavica 2013, 55:30  doi:10.1186/1751-0147-55-30

The electronic version of this article is the complete one and can be found online at: http://www.actavetscand.com/content/55/1/30


Received:11 September 2012
Accepted:6 April 2013
Published:12 April 2013

© 2013 Nathues et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Mycoplasma hyopneumoniae is the etiologic agent of enzootic pneumonia mainly occurring in fattening pigs. It is assumed that horizontal transmission of the pathogen during nursery and growing phase starts with few suckling pigs vertically infected by the sow. The aim of the present study was the exploration of the herd prevalence of M. hyopneumoniae infections in suckling pigs followed by an investigation of various herd specific factors for their potential of influencing the occurrence of this pathogen at the age of weaning.

Results

In this cross-sectional study, 125 breeding herds were examined by taking nasal swabs from 20 suckling pigs in each herd. In total, 3.9% (98/2500) of all nasal swabs were tested positive for M. hyopneumoniae by real-time PCR. Piglets tested positive originated from 46 different herds resulting in an overall herd prevalence of 36.8% (46/125) for M. hyopneumoniae infection in pigs at the age of weaning. While the herds were epidemiologically characterized, the risk for demonstration of M. hyopneumoniae was significantly increased, when the number of purchased gilts per year was more than 120 (OR: 5.8), and when the number of farrowing pens per compartment was higher than 16 (OR: 3.3). In herds with a planned and segregated production, where groups of sows entered previously emptied farrowing units, the risk for demonstration of M. hyopneumoniae in piglets was higher in herds with two or four weeks between batches than in herds with one or three weeks between batches (OR: 2.7).

Conclusions

In this cross-sectional study, several risk factors could be identified enhancing the probability of breeding herds to raise suckling pigs already infected with M. hyopneumoniae at the time of weaning. Interestingly, some factors (farrowing rhythm, gilt acclimatisation issues) were overlapping with those also influencing the seroprevalences among sows or the transmission of the pathogen between older age groups. Taking the multifactorial character of enzootic pneumonia into account, the results of this study substantiate that a comprehensive herd specific prevention programme is a prerequisite to reduce transmission of and disease caused by M. hyopneumoniae.

Keywords:
Mycoplasma hyopneumoniae; Enzootic pneumonia; Suckling pig; Epidemiology; Risk factor analysis; Prevalence

Background

Despite more than four decades of attempts to control porcine enzootic pneumonia [1,2], which also included more than fifteen years of vaccination against Mycoplasma hyopneumoniae, the etiologic agent is still widespread in nearly all pig populations. Noteworthy, enzootic pneumonia has remained one of the most important respiratory diseases in growing and fattening pigs leading to significant economic impacts on pig production throughout the world.

In general, the pathogen is transmitted nose to nose by vertical route from sows to their offspring [3] or by very effective horizontal route between pen mates or pigs in the same compartment [4]. If the system of all-in/all-out is not consequently implemented in the different production stages, there are also frequent transmissions of M. hyopneumoniae from older, infected to younger, naïve pigs [5]. It is assumed that suckling pigs from gilts and young sows, which are shedding M. hyopneumoniae more often than middle aged sows, have a higher risk of becoming positive by vertical transmission [6]. Despite this, the seroprevalence of M. hyopneumoniae differ between endemically infected herds, which probably reflect the pathogen load of the herds. In some herds older sows are more often seropositive than younger ones [7]. Noteworthy, seropositivity is not necessarily correlated with the shedding of M. hyopneumoniae[6] and more research is required to determine how sow parity affects the shedding of M. hyopneumoniae[8].

Next to these risk factors considering the age of the sows, vaccination of sows against M. hyopneumoniae has been described potentially influencing the vertical transmission of the pathogen and course of enzootic pneumonia in growing pigs [9].

Above all, no other potential risk factors for the occurrence of M. hyopneumoniae in piglets at the age of weaning considering the management, hygiene measures, vaccination programmes and husbandry systems on herd level have been characterised in detail. Since it is assumed that horizontal transmission of M. hyopneumoniae during nursery and growing phase starts with few vertically infected piglets [10] knowledge about these risk factors seems to be a prerequisite for efficient control and prevention programmes.

The aim of the present study was the exploration of the herd prevalence of M. hyopneumoniae infections in suckling pigs followed by an investigation of various herd specific factors for their potential of influencing the occurrence of this pathogen at the age of weaning. For this purpose, a cross-sectional study was conducted, where herds were epidemiologically characterised and M. hyopneumoniae status of suckling pigs was assessed by examining nasal swabs with a highly sensitive real-time PCR. It was hypothesised that more information about factors triggering the vertical transmission of M. hyopneumoniae from sows to their offspring will also improve the knowledge about horizontal transmission.

Methods

Data for this cross-sectional field study were collected between June 2009 and July 2010, thus covering all seasons of the year. All farm owners and veterinarians agreed on using the data from this study for publication except of their names and addresses. The collection of nasal swabs from pigs was not considered being an 'animal experiment according to the German Animal Welfare Act'. Nonetheless, the study was performed under a licence for experimenting on animals by the German Federal State Veterinary Administration Office in Lower Saxony (addition to study No. 33.9-42502-05-11A104, LAVES, Oldenburg, Germany).

Selection of herds

Overall, 125 breeding herds were selected from databases of four different marketing companies trading growing and slaughter weight pigs for farmers in the North-western part of Germany. Each database comprised approximately 50 breeding herds, but not all of them met the inclusion and exclusion criteria of this study. The principle inclusion factor was the production type ‘breeding herd’. It was out of interest, whether these herds were operating as one-site production (‘farrow-to-finish herds’) or two-site production systems (selling the growing pigs). Both production types have in common that the nursery unit(s) are located at the same place where the sows and their offspring were kept. Any purchase of pigs others than gilts or a replacement boar was treated as an exclusion criterion. All 125 herds of this study met the inclusion criteria.

The herds were typically managed according to a batch-wise farrowing system in conjunction with age-segregated rearing of the weaning and growing/finishing pigs, and an all-in/all-out hygiene policy at the level of the farrowing units, nurseries and fattening pig units.

Data collection

The information on herd level was captured with a structured and standardised questionnaire, consisting of 75 closed (e.g. yes/no) and 68 semi-closed (e.g. frequencies of procedures) questions on numerous aspects of herd management, husbandry and environment. All criteria collected were considered as potential risk factors for the occurrence of the M. hyopneumoniae infection in suckling pigs at the age of weaning. The questionnaire was pre-tested on ten herds by the field investigator (HW). These ten herds were not included in the intrinsic study.

All 125 herds were visited once and all questionnaires were filled out by the same investigator to avoid any interviewer variation. The investigator started the herd visit with a face-to-face interview with the producer. This was followed by an inspection of the entire pig herd where the given answers were assessed, facilitating on-site verification. Farmers´ answers not in accordance with the actual conditions were corrected by the investigator.

Sampling

In each herd, nasal swabs were collected from 20 suckling pigs aged 18 to 24 days of life. Two piglets per litter, the lightest male and female individuals each, were selected and swabbed in the ventral nasal passages of both sides. Lightest piglets were selected in order to standardise the sampling procedure without extensive randomization procedures for each litter.

The sample size needed to detect M. hyopneumoniae in at least one sample per herd was calculated based on an estimated prevalence of 15% and approximately 110 piglets in the subpopulations. This estimation was based on previous findings in other studies examining the prevalence of M. hyopneumoniae in suckling pigs [6,11,12]. In each herd, these subpopulations were comprised by 10 litters of an appropriate farrowing batch, where piglets had been at least 18 days old. An average litter size was estimated being approximately 11 piglets per litter at the time of weaning. The level of confidence was set at 95%.

Laboratory analysis

Subsequently to sampling, the nasal swabs were directly submitted to DNA isolation. The top of each swab was clipped and transferred into a reaction tube containing 1.5 mL Tris-EDTA (TE) buffer. After 30 min of incubation at 56ºC, the top of the swab was transferred into a shortened filter tip, which was placed in a new reaction tube, whereas the liquid in the primary tube was stored. The construct in the secondary tube was centrifuged at 18,000 g lasting 15 sec. Subsequently, the filter tip containing the top of the swab was discarded and the liquids of both reaction tubes were merged and mixed in a new one. After centrifugation at 18,000 g lasting 20 min, pellets were submitted to DNA isolation using a silica-membrane-based spin kit according to the manufacturer’s instructions (QIAamp DNA Mini kit, Qiagen). A swab previously dipped into TE buffer containing a modified Escherichia coli (K12 p_MYO_REP & p_MYO_ABC) served as an external positive control for successful DNA isolation and amplification in every test setup. The genetically modified strain of E. coli is carrying plasmids, which had been extended by the PCR target sequences of the REP and ABC genes [13]. Swabs dipped in pure TE buffer were used as negative control. The DNA was examined using real-time PCR amplifying sequences of the REP- and ABC-genes of M. hyopneumoniae[13]. The assay had been modified to a multiplex PCR [14] and was carried out on a AB 7500 cycler (Life-technologies).

Statistical analysis

Results from clinical examination and laboratory testing were entered into a spread-sheet program (Excel for Office 2010, http://www.microsoft.com webcite) and further analysed using SAS v9.1.2 (SAS Institute Inc. Cary, NC) and NCSS 2007 (http://www.ncss.com webcite).

A herd was defined as positive for M. hyopneumoniae when at least one nasal swab taken from the herd had a positive PCR outcome. All potential risk factors were screened for their individual association with the binary outcome (herd M. hyopneumoniae positive or negative) using a logistic regression (LR) model, and results recorded as odds ratios (OR) with related 95% confidence intervals and Wald P-values. For categorical risk factors, class frequencies and class-specific OR were assessed, and adjacent low frequency classes merged in order to reduce the number of classes and to increase the frequencies. Interval-measured risk factors were included into the LR model (a) as continuous (numerical) information (generating one OR estimate) and (b) as categorical variables after creating frequencies by quartile ranges. If the OR estimates over the quartiles were showing a linear (increasing/decreasing) trend, the assumption of linearity was considered to be met, and the interval format was retained. Otherwise the variable entered the LR model as a categorical variable. Spearman Rank correlation coefficients between all risk factors were derived. In case of substantial correlation (r >0.50) a decision was taken which of the variables in the pair was to retain for a final model.

Five multivariable models, each including only those parameters belonging to the same ‘biological context group’ (‘Herd management’, 'Farrowing’, ‘Vaccination of piglets’, ‘Replacement policy’, ‘Vaccination of replacement pigs’) that had univariable P-values <0.2, were run. Adjusted OR (corrected for the influence of the other variables in the respective models) with 95% CI and P-values were derived. P-values <0.05 were considered as significant.

Results

In this cross-sectional study 69.6% (87/125) of the herds were one-site production systems operating from farrow to finish. In contrast, 27.2% (34/125) of the herds were breeding herds, where all piglets had been sold at the end of the nursery phase. Another 3.2% (4/125) of the herds were basically piglet producers, but also reared a few pigs to market weight. The average herd size was 220 sows in the stock (median; range: 100-1,000) including 31 gilts (median; range: 1-161).

Nasal swabs for M. hyopneumoniae detection were obtained from piglets aged 21.8 days on average (mean; SD: 3.4). The average duration of the suckling period in these herds was 24.2 days (mean; SD: 3.0), the mean number of life born piglets in the corresponding litters was 12.7 (SD: 3.1) and the median parity of the sows of these litters was 4 with a range from 1 to ≥7 (Figure 1).

thumbnailFigure 1. Age structure of sows within the herds and those whose piglets were sampled.

Prevalence of M. hyopneumoniae infections in suckling pigs on herd level

In total, 3.9% (98/2500) of all nasal swabs from suckling pigs were tested positive for M. hyopneumoniae by real-time PCR. Piglets tested positive for specific genome fragments originated from 46 different herds resulting in an overall herd prevalence of 36.8% (46/125) for M. hyopneumoniae infection in suckling pigs at the age of weaning. The number of positive samples within these herds was ranging from one sample in 56.5% (26/46), two samples in 28.3% (13/46) and more than two samples in 15.2% (7/46) of the herds with a maximum of 15 positive tested samples in one herd.

Risk factor analysis

In a first step, frequencies were analyzed (Tables 1, 2, 3). Overall, 16 parameters showed a Wald P-value <0.2 in the univariable approach and were therefore considered as candidates for the final multivariable analysis (Table 4). Noteworthy, 13 of these parameters demonstrated statistical significance in the univariable analysis (Wald P-value <0.05).

Table 1. Variables and their level describing general factors, management and husbandry systems

Table 2. Variables and their level describing vaccination issues

Table 3. Variables and their level describing antimicrobial treatments

Table 4. Adjusted odds ratios (OR) and 95% confidence intervals from five risk factor groups

A reduced chance of finding M. hyopneumoniae in suckling pigs was recorded in all in-all out farrowing systems when employing batch-wise farrowing every week or every three weeks (OR: 0.36; P = 0.008). The reduction was even stronger (OR: 0.31; P = 0.015), when herds applying batch-wise farrowing every three weeks were compared only with herds employing a batch-wise farrowing every two weeks.

An increase in time before restocking the farrowing units with a new batch of sows prior to farrowing was a preventive measure (OR: 0.30; P = 0.029).

In herds, where so-called ‘one-shot’ or ‘two-shot’ vaccines against M. hyopneumoniae were applied to the suckling pigs, infections with the correspondent agent were found more frequently (OR: 3.64; P = 0.021 and OR: 3.49; P = 0.035, respectively). Similar results with an increased risk for suckling pigs to be infected with M. hyopneumoniae were seen when they received vaccines against PRRSV (OR: 2.72; P = 0.018). Further factors increasing the probability of detecting M. hyopneumoniae in nasal swabs from piglets were attributed to an air inlet into the farrowing units via the door (OR: 2.23; P = 0.038) and a maximum number of farrowing pens in a single compartment greater than 16 (OR: 1.06; P = 0.016).

Herds where either gilts or replacement boars were vaccinated against PCV2 during their acclimatization period were more likely to be classified ‘positive for M. hyopneumoniae in suckling pigs’ than herds not vaccinating their replacements (OR: 4.49; P <0.001 and OR: 6.49; P <0.001, respectively). Moreover, the detection of the agent in suckling pigs was associated with a high number of purchases of gilts per year (OR: 1.20; P = 0.015), a high ‘minimum number of gilts per purchase’ (OR: 1.03; P = 0.039), a high ‘maximum number of gilts per purchase’ (OR: 1.03; P = 0.045) and a high ‘total number of purchased gilts per year’ (OR: 1.01; P = 0.005).

From the five multivariable models, seven variables (‘Batch-wise farrowing system used in the herd’, ‘Number of farrowing pens per compartment’, ‘Vaccination of gilts against PCV2’, ‘Number of gilts purchased per year’, ‘Use of one-shot-vaccines against M. hyopneumoniae in suckling pigs’, ‘Use of two-shot-vaccine against M. hyopneumoniae in suckling pigs’ and ‘Vaccination of sucking pigs against PRRSV’) could be identified being significantly associated with the detection of M. hyopneumoniae in suckling pigs at the time of weaning (Table 4).

Discussion

A cross-sectional study including 125 herds was performed evaluating the prevalence of M. hyopneumoniae infections in suckling pigs at the age of weaning and the potential of corresponding risk factors on herd level.

The region where this study was conducted has the highest pig density in Germany (> 500 pigs/ 100 hectare agricultural used space; [15]), characterized by typical configurations of intensive pig production. Herd structures, husbandry systems and management procedures assessed during this investigation are probably highly representative for many other regions in Europe with intensive pig production. In order to minimize potential selection bias, the herds enrolled in this study were not proposed by field veterinarians but were randomly selected from databases of marketing companies. The participation in the study was voluntary, but all producers asked were willing to participate. The unexpectedly high motivation may be the result of a feeling of obligation to and a degree of economic dependence on the marketing company. Furthermore, producers were highly interested in the diagnostics and veterinary consultancy free of charge.

The transmission of M. hyopneumoniae cannot securely be prevented by vaccinating piglets or pigs against this pathogen [16]. This lack of highly effective vaccines demands for additional actions reducing the impact of M. hyopneumoniae infections on the health of pigs. Any measures lowering the proportion of suckling pigs infected by their mother sow are supposed to decrease the later spread of the agent among growers and finishers [9,17]. Whether these vertical transmissions of M. hyopneumoniae and corresponding infections in suckling pigs occur with high frequencies and, therefore, have to be considered in prevention programmes is intensively discussed. Studies conducted in single endemically infected herds or herds with a recent epidemic infection with M. hyopneumoniae revealed low prevalences of 1.5 to 3.8% in suckling pigs and 4.4 to 7.2% in nursery pigs [11], 2.6 to 13.2% in piglets 3 weeks of age [10] and 9.6% in suckling pigs prior to weaning [6]. In a retrospective study including data from more than 300 herds, comparable low prevalences of 2.0% in suckling pigs and 9.3% in nursery pigs were found [12]. In contrast to these studies, rates of over 30% have been reported previously in suckling pigs, but these studies included only a limited [17,18] or an unknown number of herds [19].

In the present study, 3.9% (98/2,500) of all suckling pigs and 36.8% (46/125) of all herds were tested positive for M. hyopneumoniae. A real-time PCR has been used to detect the pathogen in nasal swabs from suckling pigs facilitating a high sensitivity. This PCR assay showed 85 to 90% sensitivity on pig level, when lung tissue was examined and both target sequences (ABC and REP) were amplified [13]. Notwithstanding, it has also been used to determine M. hyopneumoniae infections by testing nasal swabs [20]. Taking this into account, there is evidence that both figures, the overall detection rate among suckling pigs and the prevalence of herds showing M. hyopneumoniae infections in this age group, are good estimates for the current situation in the pig population of Northern Germany. Indeed a true prevalence of 3.9% would require 58 samples per herd in order to detect M. hyopneumoniae in at least one piglet out of a group of 110 piglets, but of course this sampling fraction is not affordable and the reasonable sample size used in the present study was already bigger than in other studies. Thus, the sample size was a good compromise, even though the sampling scheme as applied is missing a maximum possible prevalence of 12.7%, when all collected samples are tested negative.

Noteworthy, the probability of detecting M. hyopneumoniae in suckling pigs was lower than reported earlier [12], but it seems to be possible in approximately one third of all herds, when the sample size is large enough. These low detection rates are not in contrast to the hypothesis that single infected suckling pigs may act as spreader in the subsequent nursery or growing units [10].

In the multivariable analysis several herd factors have been identified being associated with the detection of M. hyopneumoniae in suckling pigs at the time of weaning. Whereas three factors could be assigned to risk factors, four others are more likely to be a result than a reason of frequent infections in suckling pigs: herds had a higher chance of at least one positive piglet, when ‘one-shot’ vaccines (OR: 5.5) or ‘two-shot’ vaccines (OR: 4.7) against M. hyopneumoniae were applied to the suckling pigs. Moreover, the risk was significantly increased, when piglets were vaccinated against PRRSV (OR: 4.4) or gilts were vaccinated against PCV2 (OR: 3.6). It is hypothesised that enzootic pneumonia in fattening pigs is eventually complicated by PRRS, both reflecting endemic infections in the herd including a higher probability of vertical transmission of the pathogens from sows to their offspring, drives the farmer to the decision of vaccinating suckling pigs against M. hyopneumoniae and/or PRRSV. Similar interactions can be assumed for PCV2 and gilt vaccination. The association between M. hyopneumoniae infections and the application of different vaccines was even expected, since their use is often an economic incitement for owners of endemically infected farms.

The risk of a herd to have a M. hyopneumoniae infection among suckling pigs was increased when the total number of purchased gilts per year was higher than 120 (OR: 5.8). This observation underlines the necessity of an appropriate acclimatisation period for replacements pigs, which should last approximately four to six weeks [5]. At a certain time point, gilts should get in a close nose-to-nose contact to pigs from the stock herd [21], because transmission of M. hyopneumoniae by other vectors is insufficient for the purpose of provoked exposure [22]. It should be mentioned that sentinels for nose-to-nose contact must not re-enter the stock herd, when they developed any symptoms of infectious disease during the contact phase. Therefore, the use of old sows or nursery pigs with stunted growth, dedicated for slaughter, are highly recommended as sentinels.

The number of sows housed in compartments of the farrowing units was also associated with the outcome variable. The risk of a herd being positive in suckling pigs significantly increased, when the number of farrowing pens in one compartment was higher than 16 (OR: 3.3). Again there is doubt, whether all-in/all-out policy is strictly implemented, when farrowing units are operated with a high number of pens per compartment, although this factor is known having major impact on the prevention of transmission of M. hyopneumoniae within herds [23]. Beside this, a higher number of pens per compartment also increase the probability of housing gilts in their first parity together with older sows. These gilts shed M. hyopneumoniae more often than older sows [3,6] and by doing this enable a frequent transmission of the pathogen to their own offspring, but also to piglets of other litters via aerosol [24].

Herds, where no batch farrowing or any kind of batch-wise farrowing rhythm that does not allow simple integration of sows returning to oestrus (i.e. not 1- or 3-week rhythm) was implemented, were more often found to be positive (OR 2.7). This observation was in accordance with another study reporting higher seroprevalences towards M. hyopneumoniae in sows farrowing in a 2- or 4-week rhythm [7]. When comparing only herds with 2-week farrowing-rhythm to those with 3-week rhythm, the effect was even stronger (OR: 3.8). It can be assumed that in such herds, especially those with 2-week rhythm, a strict realisation of the all-in/all-out policy for the farrowing units is not possible and not performed, because sows which have regularly returned to oestrus approximately 21 days after insemination neither fit into the last nor into the next group. Conclusively, such sows will farrow one week earlier or one week later compared to all other sows, and if the herd does not have appropriate compartments for sows farrowing ‘out of the rhythm’ these sows will be allocated into compartments, where other sows have already farrowed or will farrow later. Taking this fairly conclusive assumption into account, it seems to be the non-compliance with the all-in/all-out policy rather than the farrowing interval that increases the likelihood of M. hyopneumoniae positivity in suckling pigs at the age of weaning.

Conclusions

In this cross-sectional study, several risk factors (more than 120 replacement gilts purchased per year, farrowing compartments with more than 16 pens, no batch farrowing or batch farrowing rhythm not easy to synchronize with the sows’ natural oestrus cycle, i.e. 2- or 4-week rhythm) could be identified enhancing the probability of breeding herds to raise suckling pigs already infected with M. hyopneumoniae at the time of weaning. Interestingly, some factors (farrowing rhythm, gilt acclimatisation issues) were overlapping with those also influencing the seroprevalences among sows or the transmission of the pathogen between older age groups. Taking the multifactorial character of enzootic pneumonia into account, the results of this study substantiate that a comprehensive herd specific prevention programme is a prerequisite to reduce transmission of and disease caused by M. hyopneumoniae.

Competing interests

The authors have no financial or personal relationship with people or organisations that could inappropriately influence or bias the content of this paper.

Authors’ contributions

EGB, MGD and HN designed the cross-sectional study and HW and SD carried out the farm visits and data collection. HW and SD performed the laboratory tests under supervision of HN. MGD assisted with statistical analysis and ASF performed statistical analysis. HN drafted the manuscript. ASF, MGD and EGB critically revised the manuscript. All authors read and approved the final manuscript.

Acknowledgements

The authors wish to thank Mechthild Busemann and Mechthild Sieve from the Field Station for Epidemiology for their excellent technical assistance. We would also like to thank the 125 farmers for helping with farm sampling, and the four marketing companies for their supply of data. Since 1st September 2011 HN was supported by a Marie Curie Intra European Fellowship within the 7th European Community Framework Programme (Grant number PIEF-GA-2010-274091).

References

  1. Aalund O, Willeberg P, Madrup M, Riemann H: Lung lesions at slaughter: associations to factors in the pig herd.

    Nord Vet Med 1976, 28:487-495. PubMed Abstract OpenURL

  2. Keller H: 30 years of swine health service.

    Schweiz Arch Tierh 1993, 135:72-78. PubMed Abstract OpenURL

  3. Maes D, Verdonck M, Deluyker H, de Kruif A: Enzootic pneumonia in pigs.

    Vet Quart 1996, 18:104-109. Publisher Full Text OpenURL

  4. Marois C, Le Carrou J, Kobisch M, Gautier-Bouchardon AV: Isolation of Mycoplasma hyopneumoniae from different sampling sites in experimentally infected and contact SPF piglets.

    Vet Microbiol 2007, 120:96-104. PubMed Abstract | Publisher Full Text OpenURL

  5. Maes D, Segales J, Meyns T, Sibila M, Pieters M, Haesebrouck F: Control of Mycoplasma hyopneumoniae infections in pigs.

    Vet Microbiol 2008, 126:297-309. PubMed Abstract | Publisher Full Text OpenURL

  6. Calsamiglia M, Pijoan C: Colonisation state and colostral immunity to Mycoplasma hyopneumoniae of different parity sows.

    Vet Rec 2000, 146:530-532. PubMed Abstract | Publisher Full Text OpenURL

  7. Grosse Beilage E, Rohde N, Krieter J: Seroprevalence and risk factors associated with seropositivity in sows from 67 herds in north-west Germany infected with Mycoplasma hyopneumoniae.

    Prev Vet Med 2009, 88:255-263. PubMed Abstract | Publisher Full Text OpenURL

  8. Sibila M, Pieters M, Molitor T, Maes D, Haesebrouck F, Segales J: Current perspectives on the diagnosis and epidemiology of Mycoplasma hyopneumoniae infection.

    Vet J 2009, 181:221-231. PubMed Abstract | Publisher Full Text OpenURL

  9. Sibila M, Bernal R, Torrents D, Riera P, Llopart D, Calsamiglia M, Segales J: Effect of sow vaccination against Mycoplasma hyopneumoniae on sow and piglet colonization and seroconversion, and pig lung lesions at slaughter.

    Vet Microbiol 2008, 127:165-170. PubMed Abstract | Publisher Full Text OpenURL

  10. Ruiz A, Utera V, Pijoan C: Effect of Mycoplasma hyopneumoniae sow vaccination on piglet colonization at weaning.

    J Swine Health Prod 2003, 11:131-135. OpenURL

  11. Sibila M, Nofrarias M, Lopez-Soria S, Segales J, Riera P, Llopart D, Calsamiglia M: Exploratory field study on Mycoplasma hyopneumoniae infection in suckling pigs.

    Vet Microbiol 2007, 121:352-356. PubMed Abstract | Publisher Full Text OpenURL

  12. Nathues H, Kubiak R, Tegeler R, Beilage E: Occurrence of Mycoplasma hyopneumoniae infections in suckling and nursery pigs in a region of high pig density.

    Vet Rec 2010, 166:194-198. PubMed Abstract | Publisher Full Text OpenURL

  13. Dubosson CR, Conzelmann C, Miserez R, Boerlin P, Frey J, Zimmermann W, Hani H, Kuhnert P: Development of two real-time PCR assays for the detection of Mycoplasma hyopneumoniae in clinical samples.

    Vet Microbiol 2004, 102:55-65. PubMed Abstract | Publisher Full Text OpenURL

  14. Giani E: A multiplex real-time PCR for the detection of Mycoplasma hyopneumoniae. Bern: Vetsuisse faculty; 2005. [PhD-Thesis] OpenURL

  15. Schweinedichte in Deutschland.

    http://www.destatis.de/jetspeed/portal/cms/Sites/destatis/Internet/DE/Presse/pm/2011/07/PD11__248__413.psml webcite

    OpenURL

  16. Thacker EL, Thacker BJ, Boetcher TB, Jayappa H: Comparison of antibody production, lymphocyte stimulation and protection induced by four commercial Mycoplasma hyopneumoniae bacterins.

    J Swine Health Prod 1998, 6:107-112. OpenURL

  17. Fano E, Pijoan C, Dee S, Deen J: Effect of Mycoplasma hyopneumoniae colonization at weaning on disease severity in growing pigs.

    Can J Vet Res 2007, 71:195-200. PubMed Abstract | PubMed Central Full Text OpenURL

  18. Villareal I, Vranckx K, Duchateau L, Pasmans F, Haesebrouck F, Jensen JC, Nanjiani IA, Maes D: Early Mycoplasma hyopneumoniae infections in European suckling pigs in herds with respiratory problems: detection rate and risk factors.

    Vet Med 2010, 55:318-324. OpenURL

  19. Palzer A, Ritzmann M, Wolf G, Heinritzi K: Detection of pathogens in broncho-alveolar lavage from pigs with respiratory diseases.

    Tieraerztl Umschau 2005, 60:550-556. OpenURL

  20. Zeeh F, Kuhnert P, Miserez R, Doherr MG, Zimmermann W: Field validation of a real-time PCR test for the detection of Mycoplasma hyopneumoniae in nasal swabs of live pigs [in German].

    Schweiz Arch Tierh 2005, 147:373-379. PubMed Abstract | Publisher Full Text OpenURL

  21. Heuser W: Gilt pool management – acclimatization and verification. St. Luis, USA: Congress of the American Association of Swine Veterinarians; 1999:469-471. PubMed Abstract OpenURL

  22. Batista L, Pijoan C, Ruiz A, Utera V, Dee S: Assessment of transmission of Mycoplasma hyopneumoniae by personnel.

    J Swine Health Prod 2004, 12:530-532. OpenURL

  23. Clark LK, Scheidt AB, Armstrong CH, Knox K, Mayrose VB: The effect of all-in/all-out management on pigs from a herd with enzootic pneumonia.

    Vet Med 1991, 86:946-951. OpenURL

  24. Stark KD, Nicolet J, Frey J: Detection of Mycoplasma hyopneumoniae by air sampling with a nested PCR assay.

    Appl Environ Microbiol 1998, 64:543-548. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL