College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, Henan, People's Republic of China.
International Joint Research Laboratory for Zoonotic Diseases of Henan, Zhengzhou, Henan, People's Republic of China.
Parasit Vectors. 2021 Jul 15;14(1):365. doi: 10.1186/s13071-021-04862-8.
Cryptosporidium is an opportunistic pathogen that infects a wide variety of vertebrates. The aim of the present study was to characterize Cryptosporidium spp. isolates from Bactrian camels and to foster further understanding of the biological characteristics of the pathogen.
Fecal specimens were collected from two 4-year-old Bactrian camels resident at the Kaifeng City Zoo in China and examined for Cryptosporidium. Fecal specimens were screened using the floatation method, and then genomic DNA was extracted from the oocysts and identified by nested-PCR amplification of the small subunit ribosomal RNA (SSU rRNA) gene, the actin gene and the Cryptosporidium oocyst wall-protein (COWP) gene. Subtype analysis was performed based on four minisatellite (MS) loci (MS1, MS2, MS3 and MS16) that were aligned and phylogenetically analyzed to determine the species and subtype of Cryptosporidium. We then established a BALB/c mice infection model and further verified the results through clinical status, pattern of oocyst excretion and histological examination.
Cryptosporidium oocyst isolates from the two Bactrian camels had an average (± standard deviation) size of 7.49 ± 0.13 × 5.70 ± 0.10 μm (n = 50). The sequencing and phylogenetic analysis confirmed the species as C. muris. Multilocus sequence typing analysis indicated that the subtypes were M13, M4, M1 and M5. Following the inoculation of BALB/c mice, we found that the prepatent period and number of oocysts per gram increased with increasing infective dose. Oocysts were first detected in the feces of BALB/c mice at 7-8 days post-infection (dpi), with levels peaking twice thereafter, at 15-16 dpi and 19-20 dpi. Histology and scanning electron microscopy studies showed that the stomach contained gastric pits filled with Cryptosporidium that adhered to the surface of gastric mucosa gland epithelial cells, causing the latter to deform, swell and become disordered.
The findings of this study indicated that oocysts isolated from Bactrian camels were from C. muris. This is the first report of C. muris isolated from camels in China. More epidemiological data are needed to understand the prevalence and transmission of C. muris in camels in different geographic areas.
隐孢子虫是一种机会性病原体,可感染多种脊椎动物。本研究旨在对双峰驼的隐孢子虫进行鉴定,以进一步了解该病原体的生物学特征。
采集中国开封市动物园的两只 4 岁双峰驼的粪便标本,采用漂浮法检查隐孢子虫。用嵌套-PCR 扩增小亚单位核糖体 RNA(SSU rRNA)基因、动蛋白基因和隐孢子虫卵囊壁蛋白(COWP)基因,从卵囊提取基因组 DNA 进行鉴定。根据 4 个微卫星(MS)位点(MS1、MS2、MS3 和 MS16)的序列分析和系统发育分析进行亚型分析,以确定隐孢子虫的种和亚型。然后建立 BALB/c 小鼠感染模型,并通过临床状态、卵囊排泄模式和组织学检查进一步验证结果。
从两只双峰驼的粪便中分离出的隐孢子虫卵囊平均大小为 7.49 ± 0.13 × 5.70 ± 0.10 μm(n = 50)。测序和系统发育分析证实该物种为鼠隐孢子虫。多位点序列分型分析表明,亚型为 M13、M4、M1 和 M5。接种 BALB/c 小鼠后,我们发现潜伏期和每克卵囊数随感染剂量的增加而增加。BALB/c 小鼠感染后 7-8 天首次在粪便中检测到卵囊,此后两次出现高峰,分别在 15-16 天和 19-20 天。组织学和扫描电镜研究表明,胃内充满了附着在胃黏膜腺上皮细胞表面的隐孢子虫,导致胃黏膜腺上皮细胞变形、肿胀和排列紊乱。
本研究结果表明,从双峰驼分离出的卵囊来源于鼠隐孢子虫。这是首次在中国骆驼中分离出鼠隐孢子虫。需要更多的流行病学数据来了解不同地理区域骆驼中鼠隐孢子虫的流行和传播。