589
Views
0
CrossRef citations to date
0
Altmetric
Original Article

Structural and antigenic characterization of a novel genotype of Mfa1 fimbriae in Porphyromonas gingivalis

, , , , , , & show all
Article: 2215551 | Received 26 Jul 2022, Accepted 12 May 2023, Published online: 21 May 2023
 

ABSTRACT

Background

Mfa1 fimbriae of the periodontal pathogen Porphyromonas gingivalis are responsible for biofilm formation and comprise five proteins: Mfa1–5. Two major genotypes, mfa170 and mfa153, encode major fimbrillin. The mfa170 genotype is further divided into the mfa170A and mfa170B subtypes. The properties of the novel mfa170B remain unclear.

Methods

Fimbriae were purified from P. gingivalis strains JI-1 (mfa170A), 1439 (mfa170B), and Ando (mfa153), and their components and their structures were analyzed. Protein expression and variability in the antigenic specificity of fimbrillins were compared using Coomassie staining and western blotting using polyclonal antibodies against Mfa170A, Mfa170B, and Mfa153 proteins. Cell surface expression levels of fimbriae were analyzed by filtration enzyme-linked immunosorbent assays.

Results

The composition and structure of the purified Mfa1 fimbriae of 1439 was similar to that of JI-1. However, each Mfa1 protein of differential subtype/genotype was specifically detected by western blotting. Mfa170B fimbriae were expressed in several strains such as 1439, JKG9, B42, 1436, and Kyudai-3. Differential protein expression and antigenic heterogeneities were detected in Mfa2–5 between strains.

Conclusion

Mfa1 fimbriae from the mfa170A and mfa170B genotypes indicated an antigenic differencesuggesting the mfa170B, is to be utilized for the novel classification of P. gingivalis.

Acknowledgments

This study was supported in part by JSPS KAKENHI, Grant No. 20K09931 (YH). The authors thank the Hanaichi Ultrastructure Research Institute, Okazaki, Japan, for performing transmission electron microscopy and Editage (www.editage.com) for English language editing.

Disclosure statement

No potential conflict of interest was reported by the authors.

Author contributions

Y. Hasegawa contributed to the conception, design, data acquisition, data analysis, and data interpretation, and drafted and critically revised the manuscript; Y. Naiki and M. Fujimoto contributed to the design, data acquisition, data analysis, and data interpretation, and drafted and critically revised the manuscript; K. Sakae, T. Iwase, N. Miwa, K. Nagano, and H. Nawa contributed to conception and data interpretation, and drafted and critically revised the manuscript. All authors provided their final approval and agreed to be accountable for all aspects of the work.

Supplementary material

Supplemental data for this article can be accessed online at https://doi.org/10.1080/20002297.2023.2215551.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.