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Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission

Vertical transmission of Bartonella infection has been reported for several mammalian species including mice and humans. Accordingly, it is commonly held that acquired immunological tolerance contributes critically to the high prevalence of Bartonellae in wild-ranging rodent populations. Here we stu...

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Autores principales: Siewert, Lena K., Dehio, Christoph, Pinschewer, Daniel D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113594/
https://www.ncbi.nlm.nih.gov/pubmed/35580143
http://dx.doi.org/10.1371/journal.ppat.1010489
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author Siewert, Lena K.
Dehio, Christoph
Pinschewer, Daniel D.
author_facet Siewert, Lena K.
Dehio, Christoph
Pinschewer, Daniel D.
author_sort Siewert, Lena K.
collection PubMed
description Vertical transmission of Bartonella infection has been reported for several mammalian species including mice and humans. Accordingly, it is commonly held that acquired immunological tolerance contributes critically to the high prevalence of Bartonellae in wild-ranging rodent populations. Here we studied an experimental model of Bartonella infection in mice to assess the impact of maternal and newborn immune defense on vertical transmission and bacterial persistence in the offspring, respectively. Congenital infection was frequently observed in B cell-deficient mothers but not in immunocompetent dams, which correlated with a rapid onset of an antibacterial antibody response in infected WT animals. Intriguingly, B cell-deficient offspring with congenital infection exhibited long-term bacteremia whereas B cell-sufficient offspring cleared bacteremia within a few weeks after birth. Clearance of congenital Bartonella infection resulted in immunity against bacterial rechallenge, with the animals mounting Bartonella-neutralizing antibody responses of normal magnitude. These observations reveal a key role for humoral immune defense by the mother and offspring in preventing and eliminating vertical transmission. Moreover, congenital Bartonella infection does not induce humoral immune tolerance but results in anti-bacterial immunity, questioning the contribution of neonatal tolerance to Bartonella prevalence in wild-ranging rodents.
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spelling pubmed-91135942022-05-18 Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission Siewert, Lena K. Dehio, Christoph Pinschewer, Daniel D. PLoS Pathog Research Article Vertical transmission of Bartonella infection has been reported for several mammalian species including mice and humans. Accordingly, it is commonly held that acquired immunological tolerance contributes critically to the high prevalence of Bartonellae in wild-ranging rodent populations. Here we studied an experimental model of Bartonella infection in mice to assess the impact of maternal and newborn immune defense on vertical transmission and bacterial persistence in the offspring, respectively. Congenital infection was frequently observed in B cell-deficient mothers but not in immunocompetent dams, which correlated with a rapid onset of an antibacterial antibody response in infected WT animals. Intriguingly, B cell-deficient offspring with congenital infection exhibited long-term bacteremia whereas B cell-sufficient offspring cleared bacteremia within a few weeks after birth. Clearance of congenital Bartonella infection resulted in immunity against bacterial rechallenge, with the animals mounting Bartonella-neutralizing antibody responses of normal magnitude. These observations reveal a key role for humoral immune defense by the mother and offspring in preventing and eliminating vertical transmission. Moreover, congenital Bartonella infection does not induce humoral immune tolerance but results in anti-bacterial immunity, questioning the contribution of neonatal tolerance to Bartonella prevalence in wild-ranging rodents. Public Library of Science 2022-05-17 /pmc/articles/PMC9113594/ /pubmed/35580143 http://dx.doi.org/10.1371/journal.ppat.1010489 Text en © 2022 Siewert 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
Siewert, Lena K.
Dehio, Christoph
Pinschewer, Daniel D.
Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title_full Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title_fullStr Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title_full_unstemmed Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title_short Adaptive immune defense prevents Bartonella persistence upon trans-placental transmission
title_sort adaptive immune defense prevents bartonella persistence upon trans-placental transmission
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113594/
https://www.ncbi.nlm.nih.gov/pubmed/35580143
http://dx.doi.org/10.1371/journal.ppat.1010489
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