Institut Agronomique et Vétérinaire Hassan II, Rabat, Morocco.
Anses, ENVA, INRA, BIPAR, Maisons-Alfort, France.
Transbound Emerg Dis. 2017 Feb;64(1):250-263. doi: 10.1111/tbed.12366. Epub 2015 Apr 27.
The prevalence of infection by Anaplasma spp. (including Anaplasma phagocytophilum) was determined using blood smear microscopy and PCR through screening of small ruminant blood samples collected from seven regions of Morocco. Co-infections of Anaplasma spp., Babesia spp, Theileria spp. and Mycoplasma spp. were investigated and risk factors for Anaplasma spp. infection assessed. A total of 422 small ruminant blood samples were randomly collected from 70 flocks. Individual animal (breed, age, tick burden and previous treatment) and flock data (GPS coordinate of farm, size of flock and livestock production system) were collected. Upon examination of blood smears, 375 blood samples (88.9%) were found to contain Anaplasma-like erythrocytic inclusion bodies. Upon screening with a large spectrum PCR targeting the Anaplasma 16S rRNA region, 303 (71%) samples were found to be positive. All 303 samples screened with the A. phagocytophilum-specific PCR, which targets the msp2 region, were found to be negative. Differences in prevalence were found to be statistically significant with regard to region, altitude, flock size, livestock production system, grazing system, presence of clinical cases and application of tick and tick-borne diseases prophylactic measures. Kappa analysis revealed a poor concordance between microscopy and PCR (k = 0.14). Agreement with PCR is improved by considering microscopy and packed cell volume (PCV) in parallel. The prevalence of double infections was found to be 1.7, 2.5 and 24% for Anaplasma-Babesia, Anaplasma-Mycoplasma and Anaplasma-Theileria, respectively. Co-infection with three or more haemoparasites was found in 1.6% of animals examined. In conclusion, we demonstrate the high burden of anaplasmosis in small ruminants in Morocco and the high prevalence of co-infections of tick-borne diseases. There is an urgent need to improve the control of this neglected group of diseases.
采用血涂片显微镜检查和 PCR 方法,对从摩洛哥 7 个地区采集的小反刍动物血液样本进行筛查,以确定无形体属(包括嗜吞噬细胞无形体)的感染流行率。调查了无形体属、巴贝斯虫属、泰勒虫属和支原体属的混合感染情况,并评估了无形体属感染的危险因素。共从 70 个羊群中随机采集了 422 份小反刍动物血液样本。采集了个体动物(品种、年龄、蜱虫负担和既往治疗情况)和羊群数据(农场的 GPS 坐标、羊群规模和牲畜生产系统)。检查血涂片时,发现 375 份(88.9%)血液样本含有类似无形体的红细胞内含物。用针对无形体 16S rRNA 区的广谱 PCR 筛查时,发现 303 份(71%)样本呈阳性。用针对 msp2 区的嗜吞噬细胞无形体特异性 PCR 对 303 份样本进行筛查,均为阴性。区域、海拔、羊群规模、牲畜生产系统、放牧系统、临床病例存在情况和蜱虫及蜱传疾病预防措施的应用情况不同,其流行率存在统计学显著差异。Kappa 分析显示,显微镜检查和 PCR 之间的一致性较差(k=0.14)。将显微镜检查和红细胞压积(PCV)平行考虑,可提高与 PCR 的一致性。发现双重感染的发生率分别为:无形体-巴贝斯虫为 1.7%、无形体-支原体为 2.5%、无形体-泰勒虫为 24%。检查的动物中有 1.6%合并感染了三种或更多种血液寄生虫。综上所述,我们证明了摩洛哥小反刍动物无形体病负担高,且蜱传疾病的混合感染率高。迫切需要改善对这组被忽视疾病的控制。