Sting Reinhard, Geiger Claudia, Rietschel Wolfram, Blazey Birgit, Schwabe Ingo, Rau Jörg, Schneider-Bühl Lisa
Chemical and Veterinary Analysis Agency Stuttgart (CVUAS), Schaflandstr. 3/3, 70736 Fellbach, Germany.
Consiliary Laboratory for Corynebacterium Pseudotuberculosis (DVG), Schaflandstr. 3/3, 70736 Fellbach, Germany.
Animals (Basel). 2022 Jun 22;12(13):1612. doi: 10.3390/ani12131612.
Alpacas are the major camelid species in Europe held for hobbies, animal-aided therapy, and commercial reasons. As a result, health-related issues associated with alpacas are of growing significance. This especially holds true for one of the most serious infectious diseases, caseous lymphadenitis, which is caused by the bacterial pathogen (.) . Our study focuses on post-mortem examinations, the laboratory diagnostic tool ELISA, and the immunoblot technique for the detection of specific antibodies against and detection of the causative pathogen in alpaca herds. We examined a total of 232 alpacas living in three herds. Four of these alpacas were submitted for post-mortem examination, revealing abscesses, apostematous and fibrinous inflammation in inner organs, pleura, and peritoneum. Serological investigation using a commercial ELISA based on phospholipase D (PLD) as antigen and an in-lab ELISA based on whole cell antigens (WCA) revealed an overall seroprevalence of 56% and 61.2%, respectively. A total of 247 alpaca sera originating from 232 animals were tested comparatively using the in-lab and the commercial ELISA and showed a substantial degree of agreement, of 89.5% (Cohen's kappa coefficient of 0.784), for both tests. Further comparative serological studies using the two ELISAs and the immunoblot technique were carried out on selected sera originating from 12 breeding stallions and six breeding mares for which epidemiological data and partial isolates were available. The results showed the immunoblot to have a sensitivity that was superior to both ELISAs. In this context, it should be emphasized that evaluation of these investigations and the epidemiological data suggest an incubation period of one to two months. Antibiotic susceptibility testing of 13 isolates based on the determination of minimal inhibitory concentrations using the broth microdilution method revealed uniform susceptibility to aminopenicillins, cephalosporines, macrolides, enrofloxacin, florfenicol, tetracycline, sulfonamid/trimethoprime, tiamulin, gentamicin, neomycin, spectinomycin, and vancomycin, but resistance to colistin, nitrofurantoin, and oxacillin.
羊驼是欧洲因爱好、动物辅助治疗及商业目的而饲养的主要骆驼科动物。因此,与羊驼相关的健康问题日益重要。对于最严重的传染病之一——干酪性淋巴结炎而言尤其如此,该病由细菌病原体(.)引起。我们的研究聚焦于尸检、实验室诊断工具酶联免疫吸附测定(ELISA)以及免疫印迹技术,以检测羊驼群体中针对(.)的特异性抗体并检测致病病原体。我们共检查了生活在三个群体中的232只羊驼。其中四只羊驼被送去做尸检,结果显示其内脏、胸膜和腹膜有脓肿、炎性肿胀和纤维蛋白性炎症。使用基于磷脂酶D(PLD)作为抗原的商用ELISA以及基于全细胞抗原(WCA)的实验室自制ELISA进行血清学调查,结果显示总体血清阳性率分别为56%和61.2%。对来自232只动物的总共247份羊驼血清分别使用实验室自制ELISA和商用ELISA进行比较检测,结果显示两种检测方法的一致性程度较高,为89.5%(科恩kappa系数为0.784)。对来自12匹种公马和6匹种母马且有流行病学数据及部分(.)分离株的选定血清,进一步使用这两种ELISA和免疫印迹技术进行了比较血清学研究。结果显示免疫印迹的敏感性优于两种ELISA。在此背景下,应强调的是,对这些调查和流行病学数据的评估表明潜伏期为一至两个月。基于肉汤微量稀释法测定最低抑菌浓度,对13株(.)分离株进行抗生素敏感性测试,结果显示它们对氨基青霉素、头孢菌素、大环内酯类、恩诺沙星、氟苯尼考、四环素、磺胺类/甲氧苄啶、替米考星、庆大霉素、新霉素、壮观霉素和万古霉素均敏感,但对黏菌素、呋喃妥因和苯唑西林耐药。