Department of Parasitology, Xiangya School of Medicine, Central South University (CSU), Changsha, Hunan, China (mainland).
Faculty of Laboratory Medicine, Xiangya School of Medicine, Central South University (CSU), Changsha, Hunan, China (mainland).
Med Sci Monit. 2019 Jan 14;25:427-435. doi: 10.12659/MSM.912997.
BACKGROUND The prevalence and intensity of schistosomiasis infection in China has decreased markedly in recent years. Therefore, more accurate methods are critically needed to ensure further control of low-intensity schistosomiasis infection. For chronic schistosomiasis patients, the detection of schistosome eggs in colorectal mucosa tissues is commonly used. This work aimed to explore differences in sensitivity of the Schistosoma japonicum (S. japonicum) retrotransposon (SjR2) gene in colon tissue from S. japonicum infected hosts and to develop an ideal method for genetic diagnosis of low-intensity schistosomiasis. MATERIAL AND METHODS Serum and colon samples were collected from mice at different time points, either post-infection (PI) or post-treatment (PT). Colorectal biopsy specimens from outpatients with schistosomiasis were collected. All samples from mice and patients, including serum as well as colon tissue containing eggs and tissue containing no eggs, were examined using the polymerase chain reaction technique. RESULTS The results showed that the SjR2 gene could be detected in all colon tissue containing at least one egg, except for when the egg was completely degraded. The positive rate of gene detection in serum was low. The results from egg-free colon tissue from around the eggs were more consistent with the actual parasitism in vivo. CONCLUSIONS The results indicate that detection of the gene in colon tissue located within a 0.5 cm distance from the eggs would be a practical and ideal method for genetic diagnosis of schistosomiasis. After the colorectal biopsy, this method can be a sensitive assisted examination to the clinical diagnosis of low-intensity schistosomiasis infection.
近年来,中国血吸虫病感染的流行率和强度显著下降。因此,迫切需要更准确的方法来确保进一步控制低强度血吸虫病感染。对于慢性血吸虫病患者,通常检测结直肠黏膜组织中的血吸虫卵。本研究旨在探讨日本血吸虫反转录转座子(SjR2)基因在感染宿主结肠组织中的敏感性差异,并开发一种用于低强度血吸虫病遗传诊断的理想方法。
在不同时间点(感染后[PI]或治疗后[PT])从感染宿主的小鼠收集血清和结肠样本。收集来自血吸虫病门诊患者的结直肠活检标本。使用聚合酶链反应技术检查所有来自小鼠和患者的样本,包括血清以及含有卵和不含有卵的结肠组织。
结果表明,除了卵完全降解外,SjR2 基因可在所有至少含有一个卵的结肠组织中检测到。血清中基因检测的阳性率较低。来自卵周围无卵的结肠组织的结果与体内实际寄生虫感染更一致。
这些结果表明,检测距离卵 0.5 厘米范围内的结肠组织中的基因是血吸虫病遗传诊断的一种实用且理想的方法。在进行直肠乙状结肠镜检查后,该方法可以作为低强度血吸虫病感染临床诊断的一种敏感辅助检查。