Literature DB >> 25695273

Red deer as maintenance host for bovine tuberculosis, Alpine region.

Maria Fink, Corina Schleicher, Monika Gonano, Wolfgang M Prodinger, Maria Pacciarini, Walter Glawischnig, Marie-Pierre Ryser-Degiorgis, Chris Walzer, Gabrielle L Stalder, Dorotea Lombardo, Hermann Schobesberger, Petra Winter, Mathias Büttner.   

Abstract

To estimate the prevalence of bovine tuberculosis in the Alpine region, we studied the epidemiology of Mycobacterium caprae in wildlife during the 2009-2012 hunting seasons. Free-ranging red deer (Cervus elaphus) were a maintenance host in a hot-spot area, mainly located in Austria.

Entities:  

Mesh:

Year:  2015        PMID: 25695273      PMCID: PMC4344270          DOI: 10.3201/eid2103.141119

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


Bovine tuberculosis has one of the broadest host ranges of any known zoonotic pathogens. In addition to cattle, bovine tuberculosis affects many wild animal populations in North America, Europe, Africa, Asia, and New Zealand. Under certain conditions, wildlife play a role as reservoir and source of infection for domestic animals. Mycobacterium caprae has been isolated from cattle, domestic goats, domestic pigs, red deer (Cervus elaphus), and wild boar (). Evidence is increasing that M. caprae is emerging in free-ranging red deer and cattle in the Alps (,).

The Study

To estimate the prevalence of bovine tuberculosis (which is caused by M. bovis and M. caprae) in wildlife in the Alps, we investigated 1,655 hunted red deer of both sexes and different ages in Austria, Germany, Switzerland (including the Principality of Liechtenstein), and Italy. The deer were hunted specifically for the study by trained hunters. A sampling/hunting plan was calculated in advance that indicated the number of animals needed in each sampling region to calculate prevalence estimates; the number was based on the red deer density of a region. The numbers of animals killed and sampled during 3 consecutive hunting seasons (2009–10, 2010–11, and 2011–12) coordinated nearly perfectly with the sampling plan that had been developed for each sampling area (Table 1). After pathomorphologic examination of carcasses (from Germany, Austria, Italy, Swiss Tessin) or samples (from Swiss St. Gall, Swiss Grisons, and Liechtenstein), we conducted microbiological analysis from sample material. Sample material included both medial retropharyngeal lymph nodes and tracheobronchial, mediastinal, and mesenteric lymph nodes and any other tissue with macroscopically visible lesions (Table 2). For bacteriologic cultivation the sample material was homogenized by using the IKA Ultra Turaxx Tube Drive System (Staufen, Germany), decontaminated with 1% N-acetyl-L-cystein solution and neutralized in phosphate buffer (pH 6.8) as recommended by the World Organisation for Animal Health (). After sedimentation, inoculation was performed on 2 growth media: Stonebrink including PACT (polymyxin B, amphotericin B, carbenicillin, and trimethoprim) and Lowenstein-Jensen with glycerin and PACT (Heipha Diagnostika, Eppelheim, Germany). After 12 weeks’ incubation, a total of 82 bacterial cultures from 59 hunted red deer from Austria, Germany, and Italy were isolated (Tables 1, 2). All isolates were identified as M. caprae whether by reversed line blotting (Geno Type MTBC, HAIN Lifescience, Nehren, Germany) or by restriction fragment length polymorphism PCR of the gyrB gene, as previously described ().
Table 1

Estimated prevalence of Mycobacterium caprae in red deer (Cervus elaphus), Alpine region, 2009–10, 2010–11, and 2011–12 hunting seasons

Study areaNo. animalsNo. M. caprae positiveEstimated prevalence (95% CI), %
Austria, total59055
Tyrol
Lechtal I1734023.1 (17.0–30.2)
Lechtal Mitte9877.1 (2.9–14.2)
Lechtal II1516.7 (0.1–32.0)
Tannheimertal3200 (0.0–9.0)
Schwarzwasser3800 (0.0–7.6)
Vorarlberg
Region 15000 (0.0–5.9)
Region 26111.6 (0.0–8.8)
Region 347612.8 (4.8–25.8)
Region 44100 (0.0–7.1)
Region 5
35
0
0 (0.0–8.3)
Switzerland, total2730
Grisons8800 (0.0–3.4)
St. Gall4800 (0.0–6.1)
Tessin8900 (0.0–3.4)
Liechtenstein
48
0
0 (0.0–6.1)
Italy, total5141
Bergamo/Brescia7711.3 (0.0–7.1)
Bolzano
East2300 (0.0–12.3)
North2900 (0.0–9.9)
South1000 (0.0–25.9)
West6000 (0.0–4.9)
Como/Lecco6100 (0.0–4.8)
Sondrio9500 (0.0–3.2)
Trento
East4100 (0.0–7.1)
West5300 (0.0–5.5)
Varese
65
0
0 (0.0–4.6)
Germany, total2783
Region 118710.5 (0.0–3.0)
Region 29122.2 (0.2–7.8)
Table 2

Mycobacterium caprae–positive red deer (Cervus elaphus) and occurrence of macroscopically visible lesions in selected lymph nodes and other tissues, Alpine region, 2009–10, 2010–11, and 2011–12 hunting seasons*

No. animals, N = 59Lymph node†
Other tissue‡
RetropharyngealMediastinalTracheobronchialMesenteric
29+NLDNLDNLDNLD
5NLDNLDNLD+NLD
4NLDNLDNLDNLDNLD
3+NLDNLD+NLD
2NLDNLD+NLDLung
1+NLD+NLDLung
1+NLDNLD+Tonsil
1NLDNLDNLDNLDParotid lymph node
2+++NLDNLD
2NLDNLD++NLD
1++++NLD
1NLD+++NLD
1+NLD++NLD
1++NLD+NLD
1NLD+NLD+NLD
1+NLD+NLDNLD
1++NLDNLDNLD
1NLDNLD+NLDNLD
1NLD+NLDNLDNLD

*NLD, no lesions detected; +, macroscopically visible lesions.
†No. animals with positive findings: retropharyngeal, 41 deer; mediastinal, 8 deer; tracheobronchial, 12 deer; mesenteric, 16 deer.
‡No. animals with positive findings: 5 deer.

*NLD, no lesions detected; +, macroscopically visible lesions.
†No. animals with positive findings: retropharyngeal, 41 deer; mediastinal, 8 deer; tracheobronchial, 12 deer; mesenteric, 16 deer.
‡No. animals with positive findings: 5 deer. Red deer with macroscopically visible lesions (purulent abscesses varying remarkably in size) were all M. caprae positive from >1 lymph nodes/tissue, and 4 animals without visible lesions were M. caprae positive (Table 2). Microscopic examination showed that lesions had thin-walled fibrous capsules, occasionally with neutrophil granulocytes and calcifications in the necrosis zone, with an increased occurrence of neutrophil granulocytes and calcifications around the necrosis zone, and with a high occurrence of epithelioid and giant cells at the inside capsule wall. The large majority of these lesions were in the lymph nodes, particularly the medial retropharyngeal lymph nodes. Lesions in the lungs, observed in 3 animals, were consistently found in combination with lesions in the tracheobronchial and mediastinal lymph nodes; lesions in the tonsils were found with lesions in the retropharyngeal lymph nodes (Table 2). The medial retropharyngeal lymph nodes and the mesenteric lymph nodes were the primary sites of infection; most of the deer had lesions in the medial retropharyngeal lymph nodes and in the mesenteric lymph nodes, either exclusively or in combination with other sites (Table 2). Furthermore, the 4 animals without visible lesions were M. caprae positive from the medial retropharyngeal lymph nodes, suggesting a very early stage of infection. M. bovis infections of cattle or deer tonsils led to bacterial colonization in the medial retropharyngeal lymph nodes with subsequent lymphatic spread to pulmonary lymph nodes. Ingestion of the M. bovis bacteria led to lymphatic spread from the primary infection, the gut, to mediastinal or tracheobronchial lymph nodes, which explained the lesions in the mesenteric lymph nodes (). M. bovis causing tuberculosis is proposed to be a lymphatic disease (); we propose the same for M. caprae. We calculated regional prevalence estimates with 95% CIs (Table 1; Figure 1). Prevalence estimates differed greatly among the sampling areas in Austria, Switzerland, Germany, and Italy. Moreover, a spatial cluster of positive samples (hot spot) around the Austrian sampling area Lechtal I was identified using point pattern analysis. The cluster comprised all positive animals from Lechtal I and the contiguous sampling areas of Lechtal Mitte, Regions 2 and 3 of Vorarlberg, and Region 1 of Bavaria (Germany) (p<0.001) (–). Consequently, this hot spot included 55 of the 59 positive samples detected in this study (Table 1; Figure 2).
Figure 1

Study area in the Alpine region showing the 22 sampling regions and the estimated prevalences of Mycobacteria caprae. Prevalence ranges are classified into 6 intervals, wherein the upper bounds are not included in the interval. Austria: Vorarlberg (V1–V5) and Tyrolean Lech valley: Lechtal I (L1), Lechtal Mitte (LM), Lechtal II (L2), Schwarzwasser (SW),and Tannheimertal (TH). Germany: Bavaria (Region 1 and Region 2). Switzerland: St. Gall, Grisons, Tessin, and Liechtenstein. Italy: Varese, Como/Lecco, Sondrio, Bergamo/Brescia, Trento, Bolzano.

Figure 2

Statistically evident spatial cluster of Mycobacterium caprae–positive red deer in the Alpine region, 2009-10, 2010-2011, and 2011-12 hunting seasons. Area in red circle contained significantly more M. caprae–positive red deer than the remaining study area (p<0.001). Inset shows location of Austria and Germany within Europe (shading).

Study area in the Alpine region showing the 22 sampling regions and the estimated prevalences of Mycobacteria caprae. Prevalence ranges are classified into 6 intervals, wherein the upper bounds are not included in the interval. Austria: Vorarlberg (V1–V5) and Tyrolean Lech valley: Lechtal I (L1), Lechtal Mitte (LM), Lechtal II (L2), Schwarzwasser (SW),and Tannheimertal (TH). Germany: Bavaria (Region 1 and Region 2). Switzerland: St. Gall, Grisons, Tessin, and Liechtenstein. Italy: Varese, Como/Lecco, Sondrio, Bergamo/Brescia, Trento, Bolzano. Statistically evident spatial cluster of Mycobacterium caprae–positive red deer in the Alpine region, 2009-10, 2010-2011, and 2011-12 hunting seasons. Area in red circle contained significantly more M. caprae–positive red deer than the remaining study area (p<0.001). Inset shows location of Austria and Germany within Europe (shading). Genotyping was performed from M. caprae isolates by spoligotyping () and by mycobacterial interspersed repetitive unit typing and variable number tandem repeat genotyping for 24 loci (). All isolates in the hot-spot area and the 2 other isolates from Austria were of the Lechtal genotype. The single isolate in Italy, located >200 km from the hot spot, was also of the Lechtal genotype, and an association might exist between this case and cattle previously imported from Austria to Italy (). By contrast, 2 isolates from Germany found in the Karwendel Mountains were of the Karwendel genotype. All other deer were negative for M. caprae and for M. bovis. After the transnational project, in the 2012–13 hunting season, the prevalence in Bavaria 1 (Germany) was 5.3%, indicating an expansion of or shift in the hot spot.

Conclusions

Our data indicate a localized bovine tuberculosis problem in wildlife in the Alps related to wildlife management strategies. Supplementary feeding is common in the hot-spot area to prevent migration and to keep red deer populations high (). In the hot-spot area, the overall density is 5.6 animals/km2, but because of aggregation, which is considered the main cause of bovine tuberculosis maintenance in wildlife, winter habitats of red deer around feeding sites have up to 46.2 animals/km2 (Statistik Austria, http://www.statistik.at) (). Low (0.5–2.5 and 2–4/km2) or medium densities (9.7 deer/km2) with prevalence estimates of 0% were found in Switzerland (Saint Gall, Liechtenstein, and Grisons, respectively) (). Brescia, the only place in Italy where M. caprae was found in red deer, is considered a high-density region (16 animals/km2), but management strategies promoting aggregation are largely absent in Italy and Switzerland (). Furthermore, red deer in the hot-spot area are a reservoir for bovine tuberculosis and are the source of M. caprae infections for domestic cattle grazing on Alpine pastures during the summer (). Molecular-epidemiologic studies indicate that M. caprae isolates from red deer and cattle are of the same genotype (). Our finding that retropharyngeal lymph nodes and mesenteric lymph nodes were often the primary site of infection suggests oral rather than aerosol transmission. Oral transmission does not require direct contact, either among red deer or between red deer and cattle.
  9 in total

1.  Mycobacterium tuberculosis subsp. caprae subsp. nov.: a taxonomic study of a new member of the Mycobacterium tuberculosis complex isolated from goats in Spain.

Authors:  A Aranaz; E Liébana; E Gómez-Mampaso; J C Galán; D Cousins; A Ortega; J Blázquez; F Baquero; A Mateos; G Súarez; L Domínguez
Journal:  Int J Syst Bacteriol       Date:  1999-07

2.  Differentiation of clinical Mycobacterium tuberculosis complex isolates by gyrB DNA sequence polymorphism analysis.

Authors:  S Niemann; D Harmsen; S Rüsch-Gerdes; E Richter
Journal:  J Clin Microbiol       Date:  2000-09       Impact factor: 5.948

3.  Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology.

Authors:  J Kamerbeek; L Schouls; A Kolk; M van Agterveld; D van Soolingen; S Kuijper; A Bunschoten; H Molhuizen; R Shaw; M Goyal; J van Embden
Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

4.  Infection of red deer, cattle, and humans with Mycobacterium bovis subsp. caprae in western Austria.

Authors:  Wolfgang M Prodinger; Angelika Eigentler; Franz Allerberger; Michael Schönbauer; Walter Glawischnig
Journal:  J Clin Microbiol       Date:  2002-06       Impact factor: 5.948

5.  Proposal for standardization of optimized mycobacterial interspersed repetitive unit-variable-number tandem repeat typing of Mycobacterium tuberculosis.

Authors:  Philip Supply; Caroline Allix; Sarah Lesjean; Mara Cardoso-Oelemann; Sabine Rüsch-Gerdes; Eve Willery; Evgueni Savine; Petra de Haas; Henk van Deutekom; Solvig Roring; Pablo Bifani; Natalia Kurepina; Barry Kreiswirth; Christophe Sola; Nalin Rastogi; Vincent Vatin; Maria Cristina Gutierrez; Maryse Fauville; Stefan Niemann; Robin Skuce; Kristin Kremer; Camille Locht; Dick van Soolingen
Journal:  J Clin Microbiol       Date:  2006-09-27       Impact factor: 5.948

6.  Isolation of Mycobacterium caprae (Lechtal genotype) from red deer (Cervus elaphus) in Italy.

Authors:  Mario Chiari; M Zanoni; L G Alborali; G Zanardi; D Avisani; S Tagliabue; A Gaffuri; M L Pacciarini; M B Boniotti
Journal:  J Wildl Dis       Date:  2014-02-05       Impact factor: 1.535

7.  Is tuberculosis a lymphatic disease with a pulmonary portal?

Authors:  Marcel A Behr; W Ray Waters
Journal:  Lancet Infect Dis       Date:  2013-11-22       Impact factor: 25.071

8.  Surveillance of bovine tuberculosis and risk estimation of a future reservoir formation in wildlife in Switzerland and Liechtenstein.

Authors:  Janne Marie Schöning; Nadine Cerny; Sarah Prohaska; Max M Wittenbrink; Noel H Smith; Guido Bloemberg; Mirjam Pewsner; Irene Schiller; Francesco C Origgi; Marie-Pierre Ryser-Degiorgis
Journal:  PLoS One       Date:  2013-01-21       Impact factor: 3.240

9.  A Two-Years' Survey on the Prevalence of Tuberculosis Caused by Mycobacterium caprae in Red Deer (Cervus elaphus) in the Tyrol, Austria.

Authors:  Karl Schoepf; Wolfgang M Prodinger; Walter Glawischnig; Erwin Hofer; Sandra Revilla-Fernandez; Johannes Hofrichter; Johannes Fritz; Josef Köfer; Friedrich Schmoll
Journal:  ISRN Vet Sci       Date:  2012-10-22
  9 in total
  15 in total

1.  Mycobacterium bovis Persistence in Two Different Captive Wild Animal Populations in Germany: a Longitudinal Molecular Epidemiological Study Revealing Pathogen Transmission by Whole-Genome Sequencing.

Authors:  Thomas A Kohl; Christian Utpatel; Stefan Niemann; Irmgard Moser
Journal:  J Clin Microbiol       Date:  2018-08-27       Impact factor: 5.948

2.  Investigation of intra-herd spread of Mycobacterium caprae in cattle by generation and use of a whole-genome sequence.

Authors:  S Broeckl; S Krebs; A Varadharajan; R K Straubinger; H Blum; M Buettner
Journal:  Vet Res Commun       Date:  2017-02-13       Impact factor: 2.459

3.  Patterns of Mycobacterium tuberculosis-complex excretion and characterization of super-shedders in naturally-infected wild boar and red deer.

Authors:  Nuno Santos; Virgílio Almeida; Christian Gortázar; Margarida Correia-Neves
Journal:  Vet Res       Date:  2015-10-30       Impact factor: 3.683

4.  Causes of mortality and morbidity in free-ranging mustelids in Switzerland: necropsy data from over 50 years of general health surveillance.

Authors:  E Akdesir; F C Origgi; J Wimmershoff; J Frey; C F Frey; M-P Ryser-Degiorgis
Journal:  BMC Vet Res       Date:  2018-06-19       Impact factor: 2.741

5.  Mycobacterium caprae Infection of Red Deer in Western Austria-Optimized Use of Pathology Data to Infer Infection Dynamics.

Authors:  Annette Nigsch; Walter Glawischnig; Zoltán Bagó; Norbert Greber
Journal:  Front Vet Sci       Date:  2019-01-21

6.  Tracing cross species transmission of Mycobacterium bovis at the wildlife/livestock interface in South Africa.

Authors:  Petronillah R Sichewo; Tiny M Hlokwe; Eric M C Etter; Anita L Michel
Journal:  BMC Microbiol       Date:  2020-03-04       Impact factor: 3.605

7.  Evaluation of Three Commercial Interferon-γ Assays in a Bovine Tuberculosis Free Population.

Authors:  Giovanni Ghielmetti; Patricia Landolt; Ute Friedel; Marina Morach; Sonja Hartnack; Roger Stephan; Sarah Schmitt
Journal:  Front Vet Sci       Date:  2021-06-10

8.  Two alternative DNA extraction methods to improve the detection of Mycobacterium-tuberculosis-complex members in cattle and red deer tissue samples.

Authors:  Shari Fell; Stephanie Bröckl; Mathias Büttner; Anna Rettinger; Pia Zimmermann; Reinhard K Straubinger
Journal:  BMC Microbiol       Date:  2016-09-15       Impact factor: 3.605

9.  Matrixlysis, an improved sample preparation method for recovery of Mycobacteria from animal tissue material.

Authors:  Christoph Leth; Ashok Varadharajan; Patrick Mester; Marlis Fischaleck; Peter Rossmanith; Friedrich Schmoll; Maria Fink
Journal:  PLoS One       Date:  2017-07-19       Impact factor: 3.240

Review 10.  Infectious Wildlife Diseases in Austria-A Literature Review From 1980 Until 2017.

Authors:  Nina Eva Trimmel; Chris Walzer
Journal:  Front Vet Sci       Date:  2020-02-21
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.