| |
Fine-tuning the space, time, and host distribution of mycobacteria in wildlife
- 作者：Christian Gortazar (1)
Maria J Torres (2)
Pelayo Acevedo (3)
Javier Aznar (2)
Juan J Negro (5)
Jose de la Fuente (1) (6)
Joaquín Vicente (1) (4)
- 刊名：BMC Microbiology
- 出版年：2011
- 出版时间：December 2011
- 年：2011
- 卷：11
- 期：1
- 全文大小：1458KB
- 参考文献：1. Blanchong JA, Scribner KT, Kravchenko AN, Winterstein SR: TB-infected deer are more closely related than non-infected deer. / Biol Lett 2007, 3:103-05. CrossRef
2. Skuce RA, Neill SD: Molecular epidemiology of Mycobacterium bovis : exploiting molecular data. / Tuberculosis 2001, 81:169-75. CrossRef
3. Aranaz A, de Juan L, Montero N, Sanchez C, Galka M, Delso C, álvarez J, Romero B, Bezos J, Vela AI, Briones V, Mateos A, Domínguez L: Bovine tuberculosis ( Mycobacterium bovis ) in wildlife in Spain. / J Clin Microbiol 2004, 42:2602-608. CrossRef
4. Gortázar C, Ferroglio E, Hofle U, Frolich K, Vicente J: Diseases shared between wildlife and livestock: a European perspective. / Eur J Wildl Res 2007, 53:241-56. CrossRef
5. Acevedo-Whitehouse K, Vicente J, Gortázar C, H?fle U, Fernandez-de-Mera IG, Amos W: Genetic resistance to bovine tuberculosis in the Iberian wild boar. / Mol Ecol 2005, 14:3209-217. CrossRef
6. Vicente J, H?fle U, Garrido JM, Fernández-de-Mera IG, Juste R, Barral M, Gortázar C: Wild boar and red deer display high prevalences of tuberculosis-like lesions in Spain. / Vet Res 2006, 37:107-19. CrossRef
7. Vicente J, H?fle U, Garrido JM, Fernandez-De-Mera IG, Acevedo P, Juste RA, Barral M, Gortázar C: Risk factors associated with prevalence of tuberculosis-like lesions in wild boar and red deer in South Central Spain. / Vet Res 2007, 38:451-64. CrossRef
8. Vicente J, H?fle U, Fernández-de-Mera IG, Gortázar C: The importance of parasite life-history and host density in predicting the impact of infections in red deer. / Oecologia 2007, 152:655-64. CrossRef
9. Acevedo P, Vicente J, Ruiz-Fons JF, Cassinello J, Gortázar C: Estimation of European wild boar relative abundance and aggregation: a novel method in epidemiological risk assessment. / Epid Infect 2007, 135:519-27. CrossRef
10. Martin-Hernando MP, H?fle U, Vicente J, Ruiz-Fons F, Vidal D, Barral M, Garrido JM, de la Fuente J, Gortázar C: Lesions associated with Mycobacterium tuberculosis Complex infection in the European wild boar. / Tuberculosis 2007, 87:360-67. CrossRef
11. Naranjo V, Acevedo-Whitehouse A, Vicente J, Gortázar C, de la Fuente J: Influence of methylmalonyl-CoA mutase alleles on resistance to bovine tuberculosis in the European wild boar ( Sus scrofa ). / Anim Genet 2008, 39:316-20. CrossRef
12. Naranjo V, Gortazar C, Vicente J, de la Fuente J: Evidence of the role of European wild boar as a reservoir of Mycobacterium tuberculosis complex. / Vet Microbiol 2008, 127:1-. CrossRef
13. Collins DM, De Lisle GW, Gabric DM: Geographic distribution of restriction types of Mycobacterium bovis isolates from brush-tailed possums ( Trichosurus vulpecula ) in New Zealand. / J Hyg (Lond) 1986, 96:431-38. CrossRef
14. Gortázar C, Vicente J, Samper S, Garrido J, Fernandez-De-Mera IG, Gavín P, Juste RA, Martín C, Acevedo P, de la Puente M, Hofle U: Molecular characterization of Mycobacterium tuberculosis complex isolates from wild ungulates in South-Central Spain. / Vet Res 2005, 36:43-2. CrossRef
15. Lutze-Wallace C, Turcotte C, Sabourin M, Berlie-Surujballi G, Barbeau Y, Watchorn D, Bell J: Spoligotyping of Mycobacterium bovis isolates found in Manitoba. / Can J Vet Res 2005, 69:143-45.
16. Baker MG, Lopez LD, Cannon MC, De Lisle W, Collins DM: Continuing Mycobacterium bovis transmission from animals to humans in New Zealand. / Epid Infect 2006, 134:1068-073. CrossRef
17. Delahay RJ, Smith GC, Barlow AM, Walker N, Harris A, Clifton-Hadley RS, Cheeseman CL: Bovine tuberculosis infection in wild mammals in the south-west region of England: a survey of prevalence and a semi-quantitative assessment of the relative risk to cattle. / Vet J 2007, 173:287-01. CrossRef
18. De Lisle GW, Kawakami RP, Yates GF, Collins DM: Isolation of Mycobacterium bovis and other mycobacterial species from ferrets and stoats. / Vet Microbiol 2008, 132:402-07. CrossRef
19. De Vos V, Raath JP, Bengis RG, Kriek NJP, Huchzermeyer H, Keet DF, Michel A: The epidemiology of tuberculosis in free ranging African buffalo ( Syncerus caffer ) in the Kruger National Park, South Africa. / Onderstepoort J Vet Res 2001, 68:119-30.
20. Michel AL, Coetzee ML, Keet DF, Maré L, Warren R, Cooper D, Bengis RG, Kremer K, van Helden P: Molecular epidemiology of Mycobacterium bovis isolates from free-ranging wildlife in South African game reserves. / Vet Microbiol 2009, 133:335-43. CrossRef
21. Gortázar C, Torres MJ, Vicente J, Acevedo P, Reglero M, de la Fuente J, Negro JJ, Aznar J: Bovine tuberculosis in Do?ana biosphere reserve: the role of wild ungulates as disease reservoirs in the last Iberian lynx strongholds. / PLoS ONE 2008, 3:e2776. CrossRef
22. Zanella G, Durand B, Hars J, Moutou F, Garin-Bastuji B, Duvauchelle A, Femé M, Karoui C, Boschiroli ML: Mycobacterium bovis in wildlife in France. / J Wildlife Dis 2008, 44:99-08.
23. Woodroffe R, Donnelly CA, Johnston WT, Bourne FJ, Cheeseman CL, Clifton-Hadley RS, Cox DR, Gettinby RG, le Fevre AM, McInerney JP, Morrison WI: Spatial association of Mycobacterium bovis infection in cattle and badgers Meles meles . / J Appl Ecol 2005, 42:852-62. CrossRef
24. Jenkins HE, Woodroffe R, Donnelly CA, Cox DR, Johnston WT, Bourne FJ, Cheeseman CL, Clifton-Hadley RS, Gettinby G, Gilks P, Hewinson RG, McInerney JP, Morrison WI: Effects of culling on spatial associations of Mycobacterium bovis infections in badgers and cattle. / J Appl Ecol 2007, 44:897-08. CrossRef
25. Collins DM: DNA typing of Mycobacterium bovis strains from the Castlepoint area of the Wairarapa. / N Z Vet J 1999, 47:207-09. CrossRef
26. Corner LAL, Stevenson MA, Collins DM, Morris RS: The re-emergence of Mycobacterium bovis infection in brushtail possums ( Trichosurus vulpecula ) after localised possum eradication. / N Z Vet J 2003, 51:73-0. CrossRef
27. Primm TP, Lucero CA, Falkinham JO III: Health Impacts of Environmental Mycobacteria. / Clin Microbiol Rev 2004, 17:98-06. CrossRef
28. De Baere T, Moerman M, Rigouts L, Dhooge C, Vermeersch H, Verschraegen G, Vaneechoutte M: Mycobacterium interjectum as causative agent of cervical lymphadenitis. / J Clin Microbiol 2001, 39:725-27. CrossRef
29. Fukuoka M, Matsumura Y, Kore-eda S, Iinuma Y, Miyachi Y: Cutaneous infection due to Mycobacterium interjectum in an immunosuppressed patient with microscopic polyangiitis. / Br J Dermatol 2008, 159:1382-384. CrossRef
30. van Ingen J, Boeree MJ, de Lange WC, Hoefsloot W, Bendien SA, Magis-Escurra C, Dekhuijzen R, van Soolingen D: Mycobacterium xenopi clinical relevance and determinants, the Netherlands. / Emerg Infect Dis 2008, 14:385-89. CrossRef
31. Grange JM: Environmental mycobacteria. In / Medical Microbiology. 17th edition. Edited by: Greenwood D, Slack R, Peitherer J, Barer M. Elsevier; 2007:221-27.
32. Romero B, Aranaz A, Sandoval A, Alvarez J, de Juan L, Bezos J, Sanchez C, Galka M, Fernandez P, Mateos A, Dominguez L: Persistence and molecular evolution of Mycobacterium bovis population from cattle and wildlife in Do?ana National Park revealed by genotype variation. / Vet Microbiol 2008, 132:87-5. CrossRef
33. Conner MM, Ebinger MR, Blanchong JA, Cross PC: Infectious Disease in Cervids of North America. Data, Models, and Management Challenges. / Ann NY Acad Sci 2008, 1134:146-72. CrossRef
34. Miller R, Kaneene JB, Fitzgerald SD, Schmitt SM: Evaluation of the influence of supplemental feeding of white-tailed deer ( Odocoileus virginianus ) on the prevalence of bovine tuberculosis in the Michigan wild deer population. / J Wildl Dis 2003, 39:84-5.
35. Rogers PM, Myers K: Animal distributions, landscape classification and wildlife management, Coto Do?ana, Spain. / J Appl Ecol 1980, 17:545-65. CrossRef
36. Braza F, álvarez F, Geldof R, Byloo H: Desplazamientos de ungulados silvestres a través de una zona de ecotono en Do?ana. Do?ana. / Acta Vert 1984, 11:275-87.
37. Braza F, Alvarez F: Habitat use by red deer and fallow deer in Do?ana National Park. / Misc Zool 1987, 11:363-67.
38. Saenz De Buruaga M, Lucio AJ, Purroy J: Reconocimiento de sexo y edad en especies cinegéticas. In Edited by: Diputación Foral de álava. 1991.
39. Russo C, Tortoli E, Menichella D: Evaluation of the New GenoType Mycobacterium Assay for Identification of Mycobacterial Species. / J Clin Microbiol 2006, 44:334-39. CrossRef
40. Kamerbeek J, Schouls L, Kolk A, vanAgterveld M, vanSoolingen D, Kuijper S, Bunschoten A, Molhuizen H, Shaw R, Goyal M, van Embden J: Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. / J Clin Microbiol 1997, 35:907-14.
41. Roring S, Scott A, Brittain D, Walker I, Hewinson G, Neill S, Skuce R: Development of variable-number tandem repeat typing of Mycobacterium bovis : Comparison of results with those obtained by using existing exact tandem repeats and spoligotyping. / J Clin Microbiol 2002, 40:2126-133. CrossRef
42. Supply P, Allix C, Lesjean S, Cardoso-Oelemann M, Rüsch-Gerdes S, Willery E, Savine E, de Haas P, van Deutekom H, Roring S, Bifani P, Kurepina N, Kreiswirth B, Sola C, Rastogi N, Vatin V, Gutierrez MC, Fauville M, Niemann S, Skuce R, Kremer K, Locht C, van Soolingen D: Proposal for standardization of optimized mycobacterial interspersed repetitive unit-variable number tandem repeat typing of Mycobacterium tuberculosis . / J Clin Microbiol 2006, 44:4998-510. CrossRef
43. Frothingham R, Meeker-O'Connell WA: Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats. / Microbiology 1998, 144:1189-196. CrossRef
44. Margalef R: / Ecologia. Omega; 1977.
45. Smith NH, Dale J, Inwald J, Palmer S, Gordon SV, Hewinson RG, Smith JH: The population structure of Mycobacterium bovis in Great Britain: clonal expansion. / Proc Nat Acad Sci USA 2003, 100:15271-5275. CrossRef
46. VerCauteren KC, Atwood TC, DeLiberto TJ, Smith HJ, Stevenson JS, Thomsen BV, Gidlewski T, Payeur J: Sentinel-based Surveillance of Coyotes to Detect Bovine Tuberculosis, Michigan. / Emerg Infect Dis 2008, 14:1862-869. CrossRef
47. Naranjo V, Ayoubi P, Vicente J, Ruiz-Fons F, Gortázar C, Kocan KM, de la Fuente J: Characterization of selected genes upregulated in non-tuberculous European wild boar as possible correlates of resistance to Mycobacterium bovis infection. / Vet Microbiol 2006, 116:224-31. CrossRef
48. Naranjo V, Gortázar C, Villar M, de la Fuente J: Comparative genomics and proteomics to study tissue-specific response and function in natural Mycobacterium bovis infections. / Anim Health Res Rev 2007, 8:81-8. CrossRef
49. de la Fuente J, García-García JC, Blouin EF, Saliki JT, Kocan KM: Infection of tick cells and bovine erythrocytes with one genotype of the intracellular ehrlichia Anaplasma marginale excludes infection with other genotypes. / Clin Diagn Lab Immun 2002, 9:658-68.
50. Takeda M, Ito W, Kobayashi N, Konno K, Takahashi T, Tatsuko R, Tomita N, Tanigai T, Chiba T, Yamaguchi K, Sato K, Ueki S, Kayaba H, Chihara J: Co-existence of Mycobacterium tuberculosis and Mycobacterium intracellulare in one sputum sample. / Intern Med 2008, 47:1057-0. CrossRef
51. Machackova M, Matlova L, Lamka J, Smolik J, Melicharek I, Hanzlikova M, Docekal J, Cvetnic Z, Nagy G, Lipiec M, Ocepek M, Pavlik I: Wild boar ( Sus scrofa ) as a possible vector of mycobacterial infections: review of literature and critical analysis of data from Central Europe between 1983 and 2001. / Vet Med 2003, 48:51-5.
52. Zanetti S, Bua A, Molicotti P, Delogu G, Mura A, Ortu S, Sechi LA: Identification of mycobacterial infections in wild boars in Northern Sardinia, Italy. / Acta Vet Hung 2008, 56:145-2. CrossRef
53. Bercovier H, Vincent V: Mycobacterial infections in domestic and wild animals due to Mycobacterium marinum, M. fortuitum, M. chelonae, M. porcinum, M. farcinogenes, M. smegmatis, M. scrofulaceum, M. xenopi, M. kansasii, M. simiae and M. genavense . / Rev Sci Tech 2001, 20:265-90.
54. Michel AL, Hlokwe TM, Coetzee ML, Maré L, Connoway L, Rutten VPMG, Kremer K: High Mycobacterium bovis genetic diversity in a low prevalence setting. / Vet Microbiol 2008, 126:151-59. CrossRef
55. Richardson M, Carroll NM, Engelke E, Gian D, van der Spuy , Salker F, Munch Z, Gie RP, Warren RM, Beyers N, van Helden PD: Multiple Mycobacterium tuberculosis strains in early cultures from patients in a high-incidence community setting. / J Clin Microbiol 2002, 40:2750-754. CrossRef
56. Petrelli D, Sharma MK, Wolfe J, Al-Azem A, Hershfield E, Kabani A: Strain-related virulence of the dominant Mycobacterium tuberculosis strain in the Canadian province of Manitoba. / Tuberculosis 2004, 84:317-26. CrossRef
- 作者单位：Christian Gortazar (1)
Maria J Torres (2)
Pelayo Acevedo (3)
Javier Aznar (2)
Juan J Negro (5)
Jose de la Fuente (1) (6)
Joaquín Vicente (1) (4)
1. IREC National Wildlife Research Institute (CSIC-UCLM-JCCM), Ciudad Real, Spain
2. Departamento de Microbiología, Universidad de Sevilla, Sevilla, Spain
3. Biogeography, Diversity, and Conservation Research Team, Department of Animal Biology, Faculty of Sciences, University of Malaga, E-29071, Málaga, Spain
5. Department of Evolutionary Ecology, Estación Biológica Do?ana, CSIC, Sevilla, Spain
6. Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, Oklahoma, USA
4. Servicio de Microbiología, HH UU Virgen del Rocío, Sevilla, Spain
- ISSN：1471-2180
文摘
Background We describe the diversity of two kinds of mycobacteria isolates, environmental mycobacteria and Mycobacterium bovis collected from wild boar, fallow deer, red deer and cattle in Do?ana National Park (DNP, Spain), analyzing their association with temporal, spatial and environmental factors. Results High diversity of environmental mycobacteria species and M. bovis typing patterns (TPs) were found. When assessing the factors underlying the presence of the most common types of both environmental mycobacteria and M. bovis TPs in DNP, we evidenced (i) host species differences in the occurrence, (ii) spatial structuration and (iii) differences in the degree of spatial association of specific types between host species. Co-infection of a single host by two M. bovis TPs occurred in all three wild ungulate species. In wild boar and red deer, isolation of one group of mycobacteria occurred more frequently in individuals not infected by the other group. While only three TPs were detected in wildlife between 1998 and 2003, up to 8 different ones were found during 2006-2007. The opposite was observed in cattle. Belonging to an M. bovis-infected social group was a significant risk factor for mycobacterial infection in red deer and wild boar, but not for fallow deer. M. bovis TPs were usually found closer to water marshland than MOTT. Conclusions The diversity of mycobacteria described herein is indicative of multiple introduction events and a complex multi-host and multi-pathogen epidemiology in DNP. Significant changes in the mycobacterial isolate community may have taken place, even in a short time period (1998 to 2007). Aspects of host social organization should be taken into account in wildlife epidemiology. Wildlife in DNP is frequently exposed to different species of non-tuberculous, environmental mycobacteria, which could interact with the immune response to pathogenic mycobacteria, although the effects are unknown. This research highlights the suitability of molecular typing for surveys at small spatial and temporal scales.
| |
NGLC 2004-2010.National Geological Library of China All Rights Reserved.
Add:29 Xueyuan Rd,Haidian District,Beijing,PRC. Mail Add: 8324 mailbox 100083
For exchange or info please contact us via email.
| |
