Serrano Miriam, Elguezabal Natalia, Sevilla Iker A, Geijo María V, Molina Elena, Arrazuria Rakel, Urkitza Alfonso, Jones Gareth J, Vordermeier Martin, Garrido Joseba M, Juste Ramón A
NEIKER-Tecnalia, Basque Institute for Agricultural Research and Development, Animal Health Department, Derio, Bizkaia, Spain.
Bovine Practitioner, Gernika, Bizkaia, Spain.
PLoS One. 2017 Jan 10;12(1):e0169735. doi: 10.1371/journal.pone.0169735. eCollection 2017.
Paratuberculosis vaccination in cattle has been restricted due to its possible interference with the official diagnostic methods used in tuberculosis eradication programs. To overcome this drawback, new possibilities to detect Mycobacterium bovis infected cattle in paratuberculosis vaccinated animals were studied under experimental conditions. Three groups of 5 calves each were included in the experiment: one paratuberculosis vaccinated group, one paratuberculosis vaccinated and M. bovis infected group and one M. bovis infected group. The performance of the IFN-gamma release assay (IGRA) and the skin test using conventional avian and bovine tuberculins (A- and B-PPD) but also other more specific antigens (ESAT-6/CFP10 and Rv3615c) was studied under official and new diagnostic criteria. Regarding the IGRA of vaccinated groups, when A- and B-PPD were used the sensitivity reached 100% at the first post-challenge sampling, dropping down to 40-80% in subsequent samplings. The sensitivity for the specific antigens was 80-100% and the specificity was also improved. After adapting the diagnostic criteria for the conventional antigens in the skin test, the ability to differentiate between M. bovis infected and non-infected animals included in paratuberculosis vaccinated groups was enhanced. Taking for positive a relative skin thickness increase of at least 100%, the single intradermal test specificity and sensitivity yielded 100%. The comparative intradermal test was equally accurate considering a B-PPD relative skin increase of at least 100% and greater than or equal to that produced by A-PPD. Using the specific antigens as a proteic cocktail, the specificity and sensitivity reached 100% considering the new relative and absolute cut-offs in all experimental groups (Δ≥30% and Δmm ≥ 2, respectively). Results suggest that the interference caused by paratuberculosis vaccination in cattle could be completely overcome by applying new approaches to the official tuberculosis diagnostic tests.
由于牛副结核病疫苗接种可能干扰结核病根除计划中使用的官方诊断方法,其在牛群中的接种已受到限制。为克服这一缺点,在实验条件下研究了在接种副结核病疫苗的动物中检测感染牛分枝杆菌的牛的新方法。实验包括三组,每组5头犊牛:一组接种副结核病疫苗,一组接种副结核病疫苗并感染牛分枝杆菌,一组感染牛分枝杆菌。根据官方和新的诊断标准,研究了γ-干扰素释放试验(IGRA)以及使用传统禽型和牛型结核菌素(A-和B-PPD)以及其他更特异性抗原(ESAT-6/CFP10和Rv3615c)的皮肤试验的性能。关于接种疫苗组的IGRA,当使用A-和B-PPD时,首次攻毒后采样时敏感性达到100%,在随后的采样中降至40%-80%。特异性抗原的敏感性为80%-100%,特异性也有所提高。在调整皮肤试验中传统抗原的诊断标准后,区分接种副结核病疫苗组中感染和未感染牛分枝杆菌动物的能力得到增强。将相对皮肤厚度增加至少100%判定为阳性时,单次皮内试验的特异性和敏感性均为100%。考虑到B-PPD相对皮肤增加至少100%且大于或等于A-PPD产生的增加量,比较皮内试验同样准确。使用特异性抗原作为蛋白混合物,考虑到所有实验组的新相对和绝对临界值(分别为Δ≥30%和Δmm≥2),特异性和敏感性达到100%。结果表明,通过对官方结核病诊断试验应用新方法,可以完全克服牛副结核病疫苗接种造成的干扰。