Khairnar Krishna, Parija Subhash Chandra
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry 605 006, India.
J Health Popul Nutr. 2008 Dec;26(4):418-25. doi: 10.3329/jhpn.v26i4.1883.
Saliva is an easily-accessible and a non-invasive clinical specimen alternate to blood and liver pus. An attempt was made to detect Entamoeba histolytica DNA released in the saliva of amoebic liver abscess (ALA) patients by applying 16S-like rRNA gene-based nested multiplex polymerase chain reaction (NM-PCR). The NM-PCR detected E. histolytica DNA in the saliva of eight (28.6%) of 28 ALA patients. The NM-PCR result was negative for E. histolytica DNA in the saliva of all the eight ALA patients who were tested prior to treatment with metronidazole but was positive in the saliva of eight (40%) of 20 ALA patient who were tested after therapy with metronidazole. The NM-PCR detected E. histolytica DNA in liver abscess pus of all 28 (100%) patients with ALA. The TechLab E. histolytica II enzyme-linked immunosorbent assay was positive for E. histolytica Gal/GalNAc lectin antigen in the liver abscess pus of 13 (46.4%) of the 28 ALA patients. The indirect haemagglutination (IHA) test was positive for anti-amoebic antibodies in the serum of 22 (78.6%) of the 28 ALA patients and 2 (5.7%) of 35 healthy controls. The present study, for the first time, demonstrates the release of E. histolytica DNA in the saliva of ALA patients by applying NM-PCR.
唾液是一种易于获取且非侵入性的临床标本,可替代血液和肝脓。本研究尝试通过应用基于16S样rRNA基因的巢式多重聚合酶链反应(NM-PCR)来检测阿米巴肝脓肿(ALA)患者唾液中释放的溶组织内阿米巴DNA。NM-PCR在28例ALA患者中的8例(28.6%)唾液中检测到了溶组织内阿米巴DNA。在甲硝唑治疗前检测的所有8例ALA患者唾液中,NM-PCR检测溶组织内阿米巴DNA的结果均为阴性,但在甲硝唑治疗后检测的20例ALA患者中的8例(40%)唾液中呈阳性。NM-PCR在所有28例(100%)ALA患者的肝脓肿脓液中均检测到了溶组织内阿米巴DNA。TechLab溶组织内阿米巴II酶联免疫吸附试验在28例ALA患者中的13例(46.4%)肝脓肿脓液中检测到溶组织内阿米巴Gal/GalNAc凝集素抗原呈阳性。间接血凝试验(IHA)在28例ALA患者中的22例(78.6%)血清中抗阿米巴抗体呈阳性,在35例健康对照中的2例(5.7%)呈阳性。本研究首次通过应用NM-PCR证明了ALA患者唾液中释放溶组织内阿米巴DNA。