| Autor: |
Cembranelli SB; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Souto FO; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Ferreira-Paim K; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Richinho TT; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Nunes PL; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Nascentes GA; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Ferreira TB; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Correia D; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil., Lages-Silva E; Infectious and Parasitic Diseases Unit and Parasitology Unit, Federal University of Triangulo Mineiro, Uberaba, Minas Gerais, Brazil. |
| Abstrakt: |
Entamoeba gingivalis is considered an oral commensal but demonstrates a pathogenic potential associated with periodontal disease in immunocompromised individuals. Therefore, this study evaluated the occurrence, opportunistic conditions, and intraspecific genetic variability of E. gingivalis in HIV(+)/AIDS patients. Entamoeba gingivalis was studied using fresh examination (FE), culture, and PCR from bacterial plaque samples collected from 82 HIV(+)/AIDS patients. Genetic characterization of the lower ribosomal subunit of region 18S (18S-SSU rRNA) was conducted in 9 positive samples using low-stringency single specific primer PCR (LSSP-PCR) and sequencing analysis. Entamoeba gingivalis was detected in 63.4% (52/82) of the samples. No association was detected between the presence of E. gingivalis and the CD4(+) lymphocyte count (≤200 cells/mm(3) (p = 0.912) or viral load (p = 0.429). The LSSP-PCR results helped group E. gingivalis populations into 2 polymorphic groups (68.3% similarity): group I, associated with 63.6% (7/11) of the samples, and group II, associated with 36.4% (4/11) of the samples, which shared 74% and 83.7% similarity and association with C and E isolates from HIV(-) individuals, respectively. Sequencing of 4 samples demonstrated 99% identity with the reference strain ATCC 30927 and also showed 2 divergent clusters, similar to those detected by LSSP-PCR. Opportunistic behavior of E. gingivalis was not detected, which may be related to the use of highly active antiretroviral therapy by all HIV(+)/AIDS patients. The high occurrence of E. gingivalis in these patients can be influenced by multifactorial components not directly related to the CD4(+) lymphocyte counts, such as cholesterol and the oral microbiota host, which could mask the potential opportunistic ability of E. gingivalis. The identification of the 18S SSU-rRNA polymorphism by LSSP-PCR and sequencing analysis provides the first evidence of genetic variability in E. gingivalis isolated from HIV patients. |
