Gazzonis Alessia Libera, Gjerde Bjørn, Villa Luca, Minazzi Stefano, Zanzani Sergio Aurelio, Riccaboni Pietro, Sironi Giuseppe, Manfredi Maria Teresa
Department of Veterinary Medicine, Università degli Studi di Milano, Via Celoria 10, 20133, Milan, Italy.
Faculty of Veterinary Medicine, Department of Food Safety and Infection Biology, Norwegian University of Life Sciences, P. O. Box 369, Sentrum, 0102, Oslo, Norway.
Parasitol Res. 2019 Apr;118(4):1271-1287. doi: 10.1007/s00436-019-06249-2. Epub 2019 Feb 20.
A sample of the diaphragm was collected from each of 100 wild boars legally hunted in the Val Grande National Park in north-western Italy and examined for the presence of Sarcocystis infection by histological and molecular methods. In histological sections, thick-walled sarcocysts consistent with those of Sarcocystis miescheriana were detected in 32 wild boars. Genomic DNA extracted from diaphragm samples was initially subjected to PCR amplification of the internal transcribed spacer 1 (ITS1) region, and 97 wild boars were found to harbour a Sarcocystis infection at this screening. Selected DNA samples were then subjected to PCR amplification and sequencing of the ITS1 region and the 18S and 28S ribosomal RNA (rRNA) genes of the nuclear ribosomal DNA unit, while all positive samples were subjected to PCR amplification of the mitochondrial cytochrome c oxidase subunit I (cox1) gene. S. miescheriana was identified in 97 wild boars (97%), while the zoonotic Sarcocystis suihominis was identified in one wild boar (1%), which also harboured S. miescheriana. Intra-specific sequence variation was found in all four DNA regions of S. miescheriana examined and in the 18S rRNA gene and ITS1 region of S. suihominis. The partial cox1 gene was amplified and sequenced from 72 isolates of S. miescheriana, yielding 43 haplotypes with pairwise sequence identities of 97.6-99.9%. These haplotypes were 79.1-79.8% identical with the cox1 sequence of S. suihominis. Phylogeny based on cox1 sequences placed S. miescheriana and S. suihominis as sister species within a clade comprising mainly Sarcocystis spp. of ruminants with felids as known or presumed definitive hosts. The same was true for the phylogeny based on 18S rRNA gene sequences.
从意大利西北部瓦尔格兰德国家公园合法捕猎的100头野猪中,每头采集一份膈膜样本,通过组织学和分子学方法检查是否存在肉孢子虫感染。在组织学切片中,在32头野猪中检测到与米氏肉孢子虫一致的厚壁肉孢子囊。从膈膜样本中提取的基因组DNA首先进行内部转录间隔区1(ITS1)区域的PCR扩增,在此筛选中发现97头野猪感染了肉孢子虫。然后对选定的DNA样本进行ITS1区域以及核糖体DNA单元的18S和28S核糖体RNA(rRNA)基因的PCR扩增和测序,而所有阳性样本进行线粒体细胞色素c氧化酶亚基I(cox1)基因的PCR扩增。在97头野猪(97%)中鉴定出米氏肉孢子虫,在1头野猪(1%)中鉴定出人兽共患的猪人肉孢子虫,该野猪同时也感染了米氏肉孢子虫。在所检测的米氏肉孢子虫的所有四个DNA区域以及猪人肉孢子虫的18S rRNA基因和ITS1区域中均发现种内序列变异。从72株米氏肉孢子虫分离株中扩增并测序了部分cox1基因,产生了43个单倍型,两两序列同一性为97.6 - 99.9%。这些单倍型与猪人肉孢子虫cox1序列的同一性为79.1 - 79.8%。基于cox1序列的系统发育分析将米氏肉孢子虫和猪人肉孢子虫作为姐妹种置于一个主要由以猫科动物为已知或推测终末宿主的反刍动物肉孢子虫属物种组成的进化枝内。基于18S rRNA基因序列的系统发育分析也是如此。