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Yersinia pestis Caf1 Protein: Effect of Sequence Polymorphism on Intrinsic Disorder Propensity, Serological
Pavel Kh Kopylov1, Mikhail E Platonov1, Vitaly G Ablamunits2
1State Research Center for Applied Microbiology and Biotechnology, Obolensk, Moscow Region, Russia.
Abstract:
Yersinia pestis Caf1 is a multifunctional protein responsible for antiphagocytic activity and is a key protective antigen. It is generally conserved between globally distributed Y. pestis strains, but Y. pestis subsp. microtus biovar caucasica strains circulating within populations of common voles in Georgia and Armenia were reported to carry a single substitution of alanine to serine. We investigated polymorphism of the Caf1 sequences among other Y. pestis subsp. microtus strains, which have a limited virulence in guinea pigs and in humans. Sequencing of caf1 genes from 119 Y. pestis strains belonging to different biovars within subsp. microtus showed that the Caf1 proteins exist in three isoforms, the global type Caf1NT1 (Ala48 Phe117), type Caf1NT2 (Ser48 Phe117) found in Transcaucasian-highland and Pre-Araks natural plague foci #4-7, and a novel Caf1NT3 type (Ala48 Val117) endemic in Dagestan-highland natural plague focus #39. Both minor types are the progenies of the global isoform. In this report, Caf1 polymorphism was analyzed by comparing predicted intrinsic disorder propensities and potential protein-protein interactivities of the three Caf1 isoforms. The analysis revealed that these properties of Caf1 protein are minimally affected by its polymorphism. All protein isoforms could be equally detected by an immunochromatography test for plague at the lowest protein concentration tested (1.0 ng/mL), which is the detection limit. When compared to the classic Caf1NT1 isoform, the endemic Caf1NT2 or Caf1NT3 had lower immunoreactivity in ELISA and lower indices of self- and cross-protection. Despite a visible reduction in cross-protection between all Caf1 isoforms, our data suggest that polymorphism in the caf1 gene may not allow the carriers of Caf1NT2 or Caf1NT3 variants escaping from the Caf1NT1-mediated immunity to plague in the case of a low-dose flea-borne infection.
Insights
Yersinia pestis Caf1 protein variations (isoforms) show minimal impact on plague detection but reduced immune protection. These Yersinia pestis variants may not evade Caf1NT1 immunity during low-dose infections.
Area of Science:
- Microbiology
- Immunology
- Genetics
Background:
- Yersinia pestis Caf1 protein is crucial for antiphagocytic activity and serves as a key protective antigen.
- Caf1 is generally conserved, but variations exist, notably in Y. pestis subsp. microtus strains.
Purpose of the Study:
- To investigate the polymorphism of Caf1 sequences in Y. pestis subsp. microtus strains.
- To analyze the impact of Caf1 protein isoforms on intrinsic disorder, protein interactions, and immunoreactivity.
Main Methods:
- Sequencing of caf1 genes from 119 Y. pestis strains.
- Bioinformatic analysis of predicted intrinsic disorder propensities and protein-protein interactions.
- Detection using immunochromatography and enzyme-linked immunosorbent assay (ELISA).
Main Results:
- Three Caf1 isoforms were identified: Caf1NT1 (global), Caf1NT2, and a novel Caf1NT3.
- Polymorphism minimally affected intrinsic disorder and protein interaction properties.
- All isoforms were detectable at 1.0 ng/mL by immunochromatography.
- Caf1NT2 and Caf1NT3 exhibited lower immunoreactivity and reduced self- and cross-protection compared to Caf1NT1.
Conclusions:
- Yersinia pestis Caf1 protein polymorphism has minimal impact on detection limits.
- Despite reduced immunoreactivity and cross-protection, Caf1NT2 and Caf1NT3 variants may not enable escape from Caf1NT1-mediated immunity in low-dose infections.
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