Remarkable genetic variability and high antigenicity of the octapeptide‐repeat region in an <i>Entamoeba nuttalli</i>‐specific surface protein

Entamoeba nuttalli is genetically the closest to Entamoeba histolytica, the causative agent of human amebiasis. E. nuttalli is found in Macaca species, exhibiting no symptoms while potentially virulent. Using comparative genomics of Entamoeba species, we identified a gene encoding an E. nuttalli-specific protein containing 42 repeats of an octapeptide (PTORS). In the present study, we analyzed the genes in E. nuttalli strains derived from various geographic locations and host species. Sequence analysis of genomic DNA from four strains indicated 43, 44, and 48 repeat types in addition to 42 repeats and remarkable genetic diversity in the repeat region, although all nucleotide substitutions were synonymous. In contrast, the sequences of the N-terminal side region and C-terminus were identical among the strains. Monoclonal antibodies prepared against recombinant PTORS were reactive to the repeat regions but not to the N-terminal side regions. Polyclonal antibodies did not react with the N-terminal region, demonstrating that the repeat region had higher antigenicity. Analysis using synthetic peptides revealed that the two repeats of the octapeptide functioned as epitopes. Immunofluorescence microscopy using monoclonal antibodies demonstrated the surface localization of PTORS. These results suggest that the repeat region of PTORS plays an important role in host-parasite interactions.

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Publication Details

Journal
Journal of Eukaryotic Microbiology
Published
2024-08-19
DOI
https://doi.org/10.1111/jeu.13055
Primary Topic
Amoebic Infections and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Remarkable genetic variability and high antigenicity of the octapeptide‐repeat region in an Entamoeba nuttalli‐specific surface protein

Akitomo Sugawara, Hiroshi Tachibana, Xunjia Cheng, Tatsuya Imai et al.
Journal of Eukaryotic Microbiology
Amoebic Infections and Treatments
article

Remarkable genetic variability and high antigenicity of the octapeptide‐repeat region in an Entamoeba nuttalli‐specific surface protein

Akitomo Sugawara, Hiroshi Tachibana, Xunjia Cheng, Tatsuya Imai, Azumi Kakino
article en

Abstract

Entamoeba nuttalli is genetically the closest to Entamoeba histolytica, the causative agent of human amebiasis. E. nuttalli is found in Macaca species, exhibiting no symptoms while potentially virulent. Using comparative genomics of Entamoeba species, we identified a gene encoding an E. nuttalli-specific protein containing 42 repeats of an octapeptide (PTORS). In the present study, we analyzed the genes in E. nuttalli strains derived from various geographic locations and host species. Sequence analysis of genomic DNA from four strains indicated 43, 44, and 48 repeat types in addition to 42 repeats and remarkable genetic diversity in the repeat region, although all nucleotide substitutions were synonymous. In contrast, the sequences of the N-terminal side region and C-terminus were identical among the strains. Monoclonal antibodies prepared against recombinant PTORS were reactive to the repeat regions but not to the N-terminal side regions. Polyclonal antibodies did not react with the N-terminal region, demonstrating that the repeat region had higher antigenicity. Analysis using synthetic peptides revealed that the two repeats of the octapeptide functioned as epitopes. Immunofluorescence microscopy using monoclonal antibodies demonstrated the surface localization of PTORS. These results suggest that the repeat region of PTORS plays an important role in host-parasite interactions.

Journal of Eukaryotic MicrobiologyVol. 71(6)
Tokai University (JP), Shanghai Medical College of Fudan University (CN)
Japan Society for the Promotion of Science
Life in Land
Openalex Percentile: Top 83%
Amoebic Infections and Treatments
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Remarkable genetic variability and high antigenicity of the octapeptide‐repeat region in an <i>Entamoeba nuttalli</i>‐specific surface protein — Akitomo Sugawara, Hiroshi Tachibana, et al. · Journal of Eukaryotic Microbiology (2024) | TGRS Research Map | TGRS