Expansion of Variant Diversity Associated with a High Prevalence of Pathogen Strain Superinfection under Conditions of Natural Transmission

Author:

Ueti Massaro W.1,Tan Yunbing2,Broschat Shira L.23,Castañeda Ortiz Elizabeth J.4,Camacho-Nuez Minerva4,Mosqueda Juan J.5,Scoles Glen A.1,Grimes Matthew3,Brayton Kelly A.36,Palmer Guy H.36

Affiliation:

1. Animal Diseases Research Unit, USDA-ARS, Pullman, Washington, USA

2. School of Electrical Engineering and Computer Science, Washington State University, Pullman, Washington, USA

3. Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington, USA

4. Posgrado en Ciencias Genomicas, Universidad Autónoma de la Ciudad de Mexico, Mexico D.F., México

5. Universidad Autónoma de Querétaro, Campus Juriquilla, México

6. Paul G. Allen School for Global Animal Health, Washington State University, Pullman, Washington, USA

Abstract

ABSTRACT Superinfection occurs when a second, genetically distinct pathogen strain infects a host that has already mounted an immune response to a primary strain. For antigenically variant pathogens, the primary strain itself expresses a broad diversity of variants over time. Thus, successful superinfection would require that the secondary strain express a unique set of variants. We tested this hypothesis under conditions of natural transmission in both temperate and tropical regions where, respectively, single-strain infections and strain superinfections of the tick-borne pathogen Anaplasma marginale predominate. Our conclusion that strain superinfection is associated with a significant increase in variant diversity is supported by progressive analysis of variant composition: (i) animals with naturally acquired superinfection had a statistically significantly greater number of unique variant sequences than animals either experimentally infected with single strains or infected with a single strain naturally, (ii) the greater number of unique sequences reflected a statistically significant increase in primary structural diversity in the superinfected animals, and (iii) the increase in primary structural diversity reflected increased combinations of the newly identified hypervariable microdomains. The role of population immunity in establishing temporal and spatial patterns of infection and disease has been well established. The results of the present study, which examined strain structure under conditions of natural transmission and population immunity, support that high levels of endemicity also drive pathogen divergence toward greater strain diversity.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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