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Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature

Pathogen life history theory assumes a positive relationship between pathogen load in host tissues and pathogen transmission. Empirical evidence for this relationship is surprisingly rare due to the difficulty of measuring transmission for many pathogens. The comparative method, where a common host...

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Autores principales: Zinck, Christopher B., Raveendram Thampy, Prasobh, Uhlemann, Eva-Maria E., Adam, Hesham, Wachter, Jenny, Suchan, Danae, Cameron, Andrew D. S., Rego, Ryan O. M., Brisson, Dustin, Bouchard, Catherine, Ogden, Nicholas H., Voordouw, Maarten J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473547/
https://www.ncbi.nlm.nih.gov/pubmed/37607182
http://dx.doi.org/10.1371/journal.ppat.1011572
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author Zinck, Christopher B.
Raveendram Thampy, Prasobh
Uhlemann, Eva-Maria E.
Adam, Hesham
Wachter, Jenny
Suchan, Danae
Cameron, Andrew D. S.
Rego, Ryan O. M.
Brisson, Dustin
Bouchard, Catherine
Ogden, Nicholas H.
Voordouw, Maarten J.
author_facet Zinck, Christopher B.
Raveendram Thampy, Prasobh
Uhlemann, Eva-Maria E.
Adam, Hesham
Wachter, Jenny
Suchan, Danae
Cameron, Andrew D. S.
Rego, Ryan O. M.
Brisson, Dustin
Bouchard, Catherine
Ogden, Nicholas H.
Voordouw, Maarten J.
author_sort Zinck, Christopher B.
collection PubMed
description Pathogen life history theory assumes a positive relationship between pathogen load in host tissues and pathogen transmission. Empirical evidence for this relationship is surprisingly rare due to the difficulty of measuring transmission for many pathogens. The comparative method, where a common host is experimentally infected with a set of pathogen strains, is a powerful approach for investigating the relationships between pathogen load and transmission. The validity of such experimental estimates of strain-specific transmission is greatly enhanced if they can predict the pathogen population strain structure in nature. Borrelia burgdorferi is a multi-strain, tick-borne spirochete that causes Lyme disease in North America. This study used 11 field-collected strains of B. burgdorferi, a rodent host (Mus musculus, C3H/HeJ) and its tick vector (Ixodes scapularis) to determine the relationship between pathogen load in host tissues and lifetime host-to-tick transmission (HTT). Mice were experimentally infected via tick bite with 1 of 11 strains. Lifetime HTT was measured by infesting mice with I. scapularis larval ticks on 3 separate occasions. The prevalence and abundance of the strains in the mouse tissues and the ticks were determined by qPCR. We used published databases to obtain estimates of the frequencies of these strains in wild I. scapularis tick populations. Spirochete loads in ticks and lifetime HTT varied significantly among the 11 strains of B. burgdorferi. Strains with higher spirochete loads in the host tissues were more likely to infect feeding larval ticks, which molted into nymphal ticks that had a higher probability of B. burgdorferi infection (i.e., higher HTT). Our laboratory-based estimates of lifetime HTT were predictive of the frequencies of these strains in wild I. scapularis populations. For B. burgdorferi, the strains that establish high abundance in host tissues and that have high lifetime transmission are the strains that are most common in nature.
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spelling pubmed-104735472023-09-02 Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature Zinck, Christopher B. Raveendram Thampy, Prasobh Uhlemann, Eva-Maria E. Adam, Hesham Wachter, Jenny Suchan, Danae Cameron, Andrew D. S. Rego, Ryan O. M. Brisson, Dustin Bouchard, Catherine Ogden, Nicholas H. Voordouw, Maarten J. PLoS Pathog Research Article Pathogen life history theory assumes a positive relationship between pathogen load in host tissues and pathogen transmission. Empirical evidence for this relationship is surprisingly rare due to the difficulty of measuring transmission for many pathogens. The comparative method, where a common host is experimentally infected with a set of pathogen strains, is a powerful approach for investigating the relationships between pathogen load and transmission. The validity of such experimental estimates of strain-specific transmission is greatly enhanced if they can predict the pathogen population strain structure in nature. Borrelia burgdorferi is a multi-strain, tick-borne spirochete that causes Lyme disease in North America. This study used 11 field-collected strains of B. burgdorferi, a rodent host (Mus musculus, C3H/HeJ) and its tick vector (Ixodes scapularis) to determine the relationship between pathogen load in host tissues and lifetime host-to-tick transmission (HTT). Mice were experimentally infected via tick bite with 1 of 11 strains. Lifetime HTT was measured by infesting mice with I. scapularis larval ticks on 3 separate occasions. The prevalence and abundance of the strains in the mouse tissues and the ticks were determined by qPCR. We used published databases to obtain estimates of the frequencies of these strains in wild I. scapularis tick populations. Spirochete loads in ticks and lifetime HTT varied significantly among the 11 strains of B. burgdorferi. Strains with higher spirochete loads in the host tissues were more likely to infect feeding larval ticks, which molted into nymphal ticks that had a higher probability of B. burgdorferi infection (i.e., higher HTT). Our laboratory-based estimates of lifetime HTT were predictive of the frequencies of these strains in wild I. scapularis populations. For B. burgdorferi, the strains that establish high abundance in host tissues and that have high lifetime transmission are the strains that are most common in nature. Public Library of Science 2023-08-22 /pmc/articles/PMC10473547/ /pubmed/37607182 http://dx.doi.org/10.1371/journal.ppat.1011572 Text en © 2023 Zinck et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zinck, Christopher B.
Raveendram Thampy, Prasobh
Uhlemann, Eva-Maria E.
Adam, Hesham
Wachter, Jenny
Suchan, Danae
Cameron, Andrew D. S.
Rego, Ryan O. M.
Brisson, Dustin
Bouchard, Catherine
Ogden, Nicholas H.
Voordouw, Maarten J.
Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title_full Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title_fullStr Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title_full_unstemmed Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title_short Variation among strains of Borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
title_sort variation among strains of borrelia burgdorferi in host tissue abundance and lifetime transmission determine the population strain structure in nature
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473547/
https://www.ncbi.nlm.nih.gov/pubmed/37607182
http://dx.doi.org/10.1371/journal.ppat.1011572
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