Irisarri-Gutiérrez María José, Mingo Marta Hernández-de, de Lucio Aida, Gil Horacio, Morales Lucía, Seguí Raimundo, Nacarapa Edy, Muñoz-Antolí Carla, Bornay-Llinares Fernando Jorge, Esteban José Guillermo, Carmena David
Department of Parasitology, Pharmacy Faculty, Valencia University, Av. Vicente Andrés Estellés s/n, 46100, Burjassot, Valencia, Spain.
Parasitology Service, National Centre for Microbiology, Carlos III Health Institute, Ctra. Majadahonda-Pozuelo Km 2, 28220, Majadahonda, Madrid, Spain.
Acta Trop. 2017 Jun;170:197-203. doi: 10.1016/j.actatropica.2017.03.010. Epub 2017 Mar 14.
Human immune deficiency virus (HIV) and tuberculosis (TB) infections remain major public health issues globally, particularly in sub-Saharan Africa. Impairment of both cell-mediated and humoral immunity by HIV and/or TB infections may limit the host's defences against other pathogens, including the diarrheagenic protozoan Cryptosporidium spp., Giardia intestinalis, and Entamoeba histolytica. During September-December 2015 a cross-sectional study was conducted to assess the prevalence and molecular diversity of these enteric parasites among HIV- and/or TB-infected patients at a medical reference centre in Chowke district, southern Mozambique. A total of 99 stool specimens were initially screened by direct microscopy and further confirmed and characterised by molecular methods. DNA sequence analyses of the genes encoding the small subunit ribosomal RNA and the 60-kDa glycoprotein were used for the typing and sub-typing of Cryptosporidium isolates, respectively. G. intestinalis-positive isolates by real-time PCR were subsequently typed at the glutamate dehydrogenase locus. Differential diagnosis of E. histolytica/dispar was achieved by real-time PCR. G. intestinalis (8.1%) was the enteric protozoan more frequently detected, followed by Cryptosporidium spp. (7.1%), and Entamoeba histolytica/dispar (6.1%). Two HIV-infected (but not TB-infected) patients harbour G. intestinalis and Cryptosporidium spp. co-infections. Two (29%) G. intestinalis isolates were successfully characterised, revealing the presence of known AII and novel BIV genotypes. Four (57%) Cryptosporidium isolates were unmistakeable assigned to C. hominis, identifying two (IbA10G2 and IdA22) sub-types. Cryptosporidium infections were not associated to diarrhoea in HIV-positive patients, probably because improved immune function in the affected individuals due to antiretroviral therapy. G. intestinalis was considered a non-opportunistic pathogen, whereas the presence of E. histolytica could not be confirmed by molecular methods. Based on their common presence in the studied clinical population, we recommend the effective diagnosis and treatment of these enteropathogens for improving the management of HIV and TB patients.
人类免疫缺陷病毒(HIV)和结核病(TB)感染仍是全球主要的公共卫生问题,在撒哈拉以南非洲地区尤为突出。HIV和/或TB感染对细胞介导免疫和体液免疫的损害可能会限制宿主对其他病原体的防御能力,这些病原体包括致腹泻原生动物隐孢子虫属、肠贾第虫和溶组织内阿米巴。2015年9月至12月期间,在莫桑比克南部乔克区的一个医学参考中心开展了一项横断面研究,以评估这些肠道寄生虫在HIV和/或TB感染患者中的流行情况及分子多样性。最初通过直接显微镜检查对总共99份粪便标本进行筛查,并通过分子方法进一步确认和鉴定。分别使用编码小亚基核糖体RNA的基因和60 kDa糖蛋白的DNA序列分析对隐孢子虫分离株进行分型和亚型分析。随后,对实时PCR检测为肠贾第虫阳性的分离株在谷氨酸脱氢酶基因座进行分型。通过实时PCR实现溶组织内阿米巴/迪斯帕内阿米巴的鉴别诊断。肠贾第虫(8.1%)是检出频率较高的肠道原生动物,其次是隐孢子虫属(7.1%)和溶组织内阿米巴/迪斯帕内阿米巴(6.1%)。两名HIV感染(但未感染TB)患者同时感染了肠贾第虫和隐孢子虫属。成功鉴定出两株(29%)肠贾第虫分离株,发现存在已知的AII基因型和新型BIV基因型。四株(57%)隐孢子虫分离株明确归为微小隐孢子虫,鉴定出两种亚型(IbA10G2和IdA22)。在HIV阳性患者中,隐孢子虫感染与腹泻无关,这可能是因为抗逆转录病毒疗法使受影响个体的免疫功能得到改善。肠贾第虫被认为是一种非机会性病原体,而分子方法无法确认溶组织内阿米巴的存在。基于它们在研究临床人群中的共同存在,我们建议对这些肠道病原体进行有效的诊断和治疗,以改善HIV和TB患者的管理。