I. Reil, M. Rubin, Ž. Cvetnić, M. Zdelar-Tuk, S. Duvnjak*, T. Miškić, B. Habrun, G. Kompes and S. Špičić
During regular implementation of the bovine tuberculosis-free cattle herd certification programme in the period from 2017 to 2020, the Laboratory for Bacterial Zoonoses and Molecular Diagnostics of Bacterial Diseases of Croatian Veterinary Institute Zagreb, Croatia tested material from 161 cattle from 27 holdings in 11 counties. The material was submitted following findings of pathoanatomical changes detected in the slaughter line suggesting tuberculosis, or after a positive reaction of cows to the tuberculin comparative methods. Species from the M. tuberculosis complex (M. bovis and M. caprae) were isolated from samples of 58 bovines (36%) from 16 holdings in eight counties. M. caprae was confirmed in 55 bovines (34%) originating from 13 holdings in seven counties, and M. bovis in three bovines (2%), each from a different holding in a different county.
Saprophytic mycobacteria were isolated from four bovine samples (2.5%) from three holdings in two counties, i.e., M. gordonae (1), M. celatum (1) and two unidentified species (M. sp.). Based on the obtained results, we can conclude that the main causative agent of bovine tuberculosis in the Republic of Croatia is M. caprae, which confirmed previous findings. Control of bovine tuberculosis in the Republic of Croatia is still needed and, in the future, should be further suppressed using tuberculinisation, controls on slaughter lines, depopulation of infected herds, and etiological determination of the causative agents.
Key words: Mycobacterium bovis; M. caprae; tuberculosis; cattle; Republic of Croatia
1. Mycobacterium tuberculosis complex – species that cause tuberculosis in mammals (M. tuberculosis, M. africanum, M. canetti, M. bovis, M. caprae, M. microti, M. pinnipedii, M. munghi, M. orygis, M. suricattae);
2. Mycobacterium leprae – the causative agent of leprosy in humans;
3. Non-tuberculosis mycobacteria (NTM) – includes all other species (more than 160 species) that act as opportunistic pathogens (Falkinham, 1996; Sinha et al., 2016).
Tuberculosis is a chronic infectious disease affecting a wide range of species of wild and domesticated animals and humans. In many countries, bovine tuberculosis is an epidemiological issue causing economic losses.
Domesticated and wild animals are considered reservoirs and vectors for bovine tuberculosis, and direct contact, contaminated pastures and contact with wild animals are the dominant means of disease transmission (Delahay et al., 2001; Biet et al., 2005).
In Croatia, the first infections with the species M. caprae in cattle, swine and humans were confirmed in 2006 (Cvetnić et al., 2007). A subsequent detailed study gave an incidence of the species M. caprae in 85% and M. bovis in 15% of 92 isolates obtained belonging to the M. tuberculosis complex (Špičić, 2008). As the most common cause of tuberculosis in cattle, M. caprae has also been reported in the countries of central and western Europe (Prodinger et al., 2005).
A 2009 decision of the Ministry of Agriculture, Fisheries and Rural Development marked the start of testing cattle for tuberculosis to obtain and maintain the status of tuberculosis-free herds of cattle, in accordance with the procedures and criteria laid down in the Ordinance on veterinary conditions for the trade of cattle and swine (Official Gazette 154/08). With the aim of complete eradication of the disease and obtaining the status of a tuberculosis-free country, the Veterinary Directorate of the Ministry of Agriculture adopted new measures in 2010 to begin the tuberculinisation campaign for the entire cattle population in the Republic of Croatia. This campaign led to the discovery of new hotspots in individual cattle holdings in Croatia.
All bovines with a positive reaction to tuberculosis were removed from the holding and sent to slaughter, with the mandatory sampling of organs and tissues for bacteriological confirmation of the causative agent of tuberculosis.
This paper aims to provide an overview of the bacteriological and molecular testing of samples obtained from positive cattle in the period from 2017 to 2020 and to determine the spread and presence of individual species of mycobacteria in the Republic of Croatia.
Materials and methods
Bacteriological testing. Submitted material was homogenised then decontaminated with 5% oxalic acid, with occasional stirring at room temperature. Samples were concentrated by centrifugation, then the supernatant was removed, and the sediment diluted with sterile distilled water. The obtained suspension was inoculated onto selected agar: 2 Löwenstein-Jensen agar with glycerol, 2 Löwenstein-Jensen agar without glycerol and 2 Stonebrink agar (Kent and Kubica, 1985). Eprouvettes with the inoculated material were incubated for 8 weeks at 37°C. Mycobacterial growth was first controlled after 4–7 days, then at weekly intervals. Colonies were identified based on the growth rate, morphology and Ziehl-Neelsen colouration, and after determination of acid-resistant rods.
Further identification and typing were performed using molecular methods.
Agar inoculated with bovine material that showed no growth after 8 weeks was considered a negative test and testing was completed (OIE Terrestrial Manual 2018, Section 3.4.6).
Molecular testing. DNA was extracted from the obtained bacterial cultures using a commercial kit DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions using the QIACUBE automated system for DNA isolation (Qiagen, Hilden). The obtained DNA was stored at -20°C.
Identification to the genus Mycobacterium was proven using the specific primers 16S rRNA F (5′-ACG GTG GGT ACT AGG TGT GGG TTT C-3′) and 16S rRNA R (5′-TCT GCG ATT ACT AGC GAC TCC GAC TTC A-3′) for replication of the region of the 16S rRNA gene (Huard et al., 2003) and primers TB1 (5′-GAG ATC GAG CTG GAG GAT CC-3′) and TB2 (5′-AGC TGC AGC CCA AAG GTG TT-3′) for the gene coding the 65 kDa antigen (Hance et al., 1989) that is common to all mycobacteria. Gene replication was performed with initial denaturation (95°C/15 min), followed by 35 cycles of denaturation (94°C/1 min), primer binding (60°C/1 min) and chain elongation (72°C/1 min) and the final step of chain elongation (72°C/10 min).
Isolates proven by the above method to belong to the genus Mycobacterium were further tested using the primers IS 1 (5′-CCT GCG AGC GTA GGC GTC GG-3′) and IS 2 (5′-CTC GTC CAG CGC CGC TTC GG-3′) which prove the insertion sequence IS6110 characteristic to the species of the M. tuberculosis complex (Eisenach et al., 1990). Replication was conducted with an initial denaturation at 95°C for 15 minutes, followed by 35 cycles (94°C/30 sec, 68°/1 min, 72°/1 min) and finally chain elongation at 72°C for 7 minutes.
The PCR reactive mixture in these tests contained 10 μL HotStarTaq Master Mix (Qiagen, Hilden, Germany), 6 μL water (Rnase-free Water, Qiagen, Hilden, Germany), 1 μL of each of the listed primers, and 2 μL DNA. Gene replication was performed using the device Veriti 96 Well Thermal Cycler (Applied Biosystems, California, USA). Replication products were analysed using the QIAxcel capillary electrophoresis device (Qiagen, Hilden, Germany).
Determination of species within the M. tuberculosis complex was performed using the molecular test GenoType MTBC kit (Hain Lifescience, Nehren, Germany). This kit is based on DNA strip technology and enables the identification of species that belong to the M. tuberculosis complex (M. africanum, M. bovis ssp. BCG, M. bovis ssp. bovis (M. bovis), M. bovis ssp. caprae (M. caprae), M. microti and M. tuberculosis/M. canettii.
The species determination procedure using this kit includes PCR replication using biotinylated primers and reverse hybridisation. Hybridisation includes the chemical denaturation of PCR replication products, hybridisation of single-chain biotinylated products on probe membranes, additional of streptavidin-alkaline phosphate conjugates, and interpretation of the obtained sample on the strip.
The final determination of saprophytic and potentially pathogenic species was conducted using the molecular tests GenoType CM based on the same principle as GenoType MTBC Kit (M. avium ssp., M. chelonae, M. abscessus, M. fortuitum, M. gordonae, M. intracellulare, M. scrofulaceum, M. interjectum, M. kansasii, M. malmoense, M. peregrinum, M. marinum/M. ulcerans, M. tuberculosis kompleks i M. xenopi) i GenoType AS kit (Hain Lifescience, Nehren, Germany) (M. simiae, M. mucogenicum, M. goodii, M. celatum, M. smegmatis, M. genavense, M. lentiflavum, M. heckeshornense, M. szulgai/M.intermedium, M. phlei, M. haemophilum, M. kansasii, M. ulcerans, M. gastri, M. asiaticum and M. shimoidei).
M. bovis is primarily a bovine pathogen, though it can also infect goats, horses, swine, camels, cats and dogs. In many undeveloped countries, this causative agent has high commercial significance.
Špičić (2008) conducted a detailed study in the Republic of Croatia, proving the presence of M. caprae in 85%, and M. bovis in 15% of a total of 92 samples belonging to the M. tuberculosis complex.
During 2010, these species were isolated from materials obtained from 117 bovines (90.7%) from 23 holdings (23%) in seven Croatian counties. M. caprae was confirmed in 83 bovines (70.9%) from nine holdings in four counties, M. bovis in 33 bovines (28.2%) from 14 holdings in five counties, and M. tuberculosis in only one animal (0.85%) (Špičić et al., 2011).
In the period 2017-2020, species from the M. tuberculosis complex (M. bovis and M. caprae) were isolated from the samples of 58 bovines (36%) from 16 holdings in 8 counties. M. caprae was confirmed in 55 bovines (34%) from 13 holdings in seven counties, and M. bovis in three bovines (2%), each from a different holding and a different county. Based on the obtained results, it can be concluded that the main causative agent of bovine tuberculosis in the Republic of Croatia is M. caprae, which confirms the results of earlier research. The research conducted in the countries of Central and Western Europe also corroborate this finding (Prodinger et al., 2005).
In comparison with previous studies in the Republic of Croatia, it can be concluded that the number of bovines positive for tuberculosis has declined, but that the disease remains present in nearly the same number of holdings.
It is also interesting to note the origin of samples included in the research. Of the 58 tuberculosis-positive bovines, 29 (50%) originated from other European countries, as determined by the ear tags, i.e., 18 animals from Romania, 10 from Hungary and 1 from the Czech Republic.
The prevalence of bovine tuberculosis has decreased over the past decade due to planned eradication efforts, though the disease has still not been fully eradicated.
In Croatia, controls of bovine tuberculosis are based on testing of all bovines over the age of six weeks in herds that do not have disease-free status in line with the requirements of EU legislation. Testing is based on a tuberculin skin test. Disease-free status is maintained by testing disease-free herds once every 3 years. For that purpose, Croatian territory is divided in 3 zones which are regularly tested in 3-year cycles. Positive animals are sent for slaughter, while their organs are taken for bacteriological testing for tuberculosis.
It can be concluded that control of bovine tuberculosis in the Republic of Croatia is still necessary to fulfil requirements to be recognised as a country free from bovine tuberculosis and in the future, this disease should be suppressed using tuberculinisation, slaughterhouse line controls, depopulation of infected herds, and etiological determination of causative agents. Special attention should also be focused on controlling migration and controls during animal imports to prevent the introduction and spread of the disease in the Republic of Croatia.
References [… show]
1. ARANAZ, A., D. COUSINS, A. MATEOS and L. DOMINGUEZ (2003): Elevation of Mycobacterium tuberculosis subsp. caprae Aranaz et al. 1999 to species rank as Mycobacterium caprae comb. nov., sp. nov. Int. J. Syst. Evol. Microbiol. 53, 1785-1789.
2. BIET, F., M. L. BOSCHIROLI, M. F. THOREL and L. A. GUILLOTEAU (2005): Zoonotic aspects of Mycobacterium bovis and Mycobacterium avium-intracellulare complex (MAC). Vet. Res. 36, 411-436.
3. CVETNIĆ, Ž., V. KATALINIĆ-JANKOVIĆ, B. ŠOŠTARIĆ, S. ŠPIČIĆ, M. OBROVAC, S. MARJANOVIĆ, M. BENIĆ, B. K. KIRIN and I. VICKOVIĆ (2007): Mycobacterium caprae in cattle and humans in Croatia. Int. J. Tuberc. Lung. Dis. 11, 652-658.
4. DELAHAY, R. J., C. L. CHEESEMAN and R. S. CLIFTON-HADLEY (2001): Wildlife disease reservoirs: the epidemiology of Mycobacterium bovis infection. Tuberculosis. (Edinb.) 81, 43-49.
5. EISENACH, K. D., M. D. CAVE, J. H. BATES and J. T. CRAWFORD (1990): Polymerase chain reaction amplification of a repetitive DNA sequence specific for Mycobacterium tuberculosis. J. Infect. Dis. 161, 977-981.
6. FALKINHAM, J. O. 3rd (1996): Epidemiology of infection by nontuberculous mycobacteria. Clin. Microbiol. Rev. 9, 177-215.
7. HANCE, A. J., B. GRANDCHAMP, V. LÉVY-FRÉBAULT, D. LECOSSIER, J. RAUZIER, D. BOCART and B. GICQUEL (1989): Detection and identification of mycobacteria by amplification of mycobacterial DNA. Mol. Microbiol. 3, 843-849.
8. HUARD, R. C., L. C. LAZZARINI, W. R. BUTLER, D. VAN SOOLINGEN and J. L. HO (2003): PCR-based method to differentiate the subspecies of the Mycobacterium tuberculosis complex on the basis of genomic deletions. J. Clin. Microbiol. 41, 1637-1650.
9. KENT, P. T. and G. P. KUBICA (1985): Public health mycobacteriology: a guide for the level III. U.S. Department of Health and Human Services, Centers for Disease Control, Atlanta.
10. MILLER, R. S. and S. J. SWEENEY (2013): Mycobacterium bovis (bovine tuberculosis) infection in North American wildlife: current status and opportunities for mitigation of risks of further infection in wildlife populations. Epidemiol. Infect. 141, 1357-1370.
11. PARTE, A. C. (2018): LPSN – list of prokaryotic names with standing in nomenclature (bacterio.net), 20 years on. Int. J. Syst. Evol. Microbiol. 68, 1825-1829.
12. PRODINGER, W. M., A. BRADSTATTER, L. NAUMANN, M. PACCIARINI, T. KUBICA, M. L. BORSCHIROLI, A. ARANAZ, G. NAGY, Ž. CVETNIĆ, M. OCEPEK, A. SKRYPNIK, W. ERLER, S. NIEMAN, I. PAVLIK and I. MOSER (2005): Characterization of Mycobacterium caprae isolates from Europe by mycobacterium interspersed repetitive unit genotyping. J. Clin. Microbiol. 43, 4984-4992.
13. PRODINGER, W. M., A. INDRA, O. K. KOKSALAN, Z. KILICASLAN and E. RICHTER (2014): Mycobacterium caprae infection in humans. Expert. Rev. Anti. Infect. Ther. 12, 1501-1513.
14. SINHA, P., A. GUPTA, P. PRAKAS, S. AMUPURBA, R. TRIPATHI and G. N. SRIVASTRA (2016): Differentiation of Mycobacterium tuberculosis complex from non-tubercular mycobacteria by nested multiplex PCR targeting IS6110, MTP40 and 32 kD alpha antigen encording gene fragments. BMC Infect. Dis. 16, 123-132.
15. ŠPIČIĆ, S. (2008): Molekularna epizootiologija vrsta Mycobacterium tuberculosis i Mycobacterium avium kompleksa izdvojenih iz ljudi, životinja i okoliša. Disertacija. Veterinarski fakultet Sveučilišta u Zagrebu.
16. ŠPIČIĆ, S., I. RAČIĆ, V. KATALINIĆ-JANKOVIĆ, A. LABROVIĆ, T. KIŠ, M. ZDELAR-TUK, S. DUVNJAK, B. HABRUN, G. KOMPES, A. VUJNOVIĆ i Ž. CVETNIĆ (2011): Tuberkuloza goveda u Hrvatskoj s posebnim osvrtom na postupak certifikacije stada slobodnih od tuberkuloze. Vet. stn. 42, 401-406.
Sumnjivi i pozitivni slučajevi tuberkuloze goveda u Republici Hrvatskoj od 2017. do 2020. godine
Dr. sc. Irena REIL, dr. med. vet., Hrvatski veterinrski institut, Zagreb, Hrvatska; Martina RUBIN, dr. med. vet., Uprava za veterinarstvo i sigurnost hrane, Ministarstvo poljoprivrede, Zagreb, Hrvatska; dr. sc. Željko CVETNIĆ, dr. med. vet., akademik, Hrvatski veterinarski institut, Veterinarski institut Križevci, Hrvatska; dr. sc. Maja ZDELAR-TUK, dr. med. vet., dr. sc. Sanja DUVNJAK, dipl. ing., Hrvatski veterinarski institut, Zagreb, Hrvatska; Tihana MIŠKIĆ, dr. med. vet., Uprava za veterinarstvo i sigurnost hrane, Ministarstvo poljoprivrede, Zagreb, Hrvatska; dr. sc. Boris HABRUN, dr. med. vet., izvanredni profesor, dr. sc. Gordan KOMPES, dr. med. vet., dr. sc. Silvio ŠPIČIĆ, dr. med. vet., Hrvatski veterinarski institut, Zagreb, Hrvatska
Urazdoblju od 2017. do 2020. godine tijekom redovitog provođenja programa certifikacije stada goveda slobodnih od tuberkuloze goveda bakteriološki je u Laboratoriju za bakterijske zoonoze i molekularnu dijagnostiku bakterijskih bolesti Hrvatskog veterinarskog instituta u Zagrebu, Hrvatska bio pretražen materijal 161 goveda iz 27 različitih uzgoja u 11 županija. Materijal je dostavljen nakon nalaza patoanatomskih promjena na liniji klanja koje upućuju na tuberkulozu ili komparativnom metodom nakon pozitivne reakcije goveda na tuberkulin. Vrste iz M. tuberculosis kompleksa (M. bovis i M. caprae) su izdvojene iz materijala 58 goveda (36 %) iz 16 uzgoja u osam županija.
M. caprae je utvrđen u 55 goveda (34 %) podrijetlom iz 13 uzgoja u sedam županija, a M. bovis u tri goveda (2 %) iz dva uzgoja u dvije županije. Saprofitske mikobakterije izdvojene su iz četiri uzorka goveda (2,5 %) dostavljenih iz tri uzgoja (21 %) u dvije županije i to M. gordonae (1), M. celatum (1) i dvije neidentificirane vrste (M. sp.). Na temelju dobivenih rezultata možemo zaključiti da je glavni uzročnik tuberkuloze goveda u Republici Hrvatskoj M. caprae, a koji je bio uzročnik i u prijašnjim istraživanjima. Kontrola tuberkuloze goveda u Republici Hrvatskoj i dalje je potrebna te bi se i u budućnosti trebala suzbijati na temelju tuberkulinizacije, kontrolama na liniji klanja te depopulacijom inficiranih stada i etiološkim dokazom vrste uzročnika.
Ključne riječi: Mycobacterium bovis, M. caprae, tuberkuloza, goveda, Republika Hrvatska
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