Dissection of Besnoitia besnoiti intermediate host life cycle stages: From morphology to gene expression
Cyst-forming Apicomplexa (CFA) of the Sarcocystidae have a ubiquitous presence as pathogens of humans and farm animals transmitted through the food chain between hosts with few notable exceptions. The defining hallmark of this family of obligate intracellular protists consists of their ability to re...
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Published in: | PLoS pathogens Vol. 18; no. 11; p. e1010955 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
San Francisco, CA USA
Public Library of Science
17-11-2022
Public Library of Science (PLoS) |
Subjects: | |
Online Access: | Get full text |
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Summary: | Cyst-forming Apicomplexa (CFA) of the Sarcocystidae have a ubiquitous presence as pathogens of humans and farm animals transmitted through the food chain between hosts with few notable exceptions. The defining hallmark of this family of obligate intracellular protists consists of their ability to remain for very long periods as infectious tissue cysts in chronically infected intermediate hosts. Nevertheless, each closely related species has evolved unique strategies to maintain distinct reservoirs on global scales and ensuring efficient transmission to definitive hosts as well as between intermediate hosts. Here, we present an in-depth comparative mRNA expression analysis of the tachyzoite and bradyzoite stages of
Besnoitia besnoiti
strain Lisbon14 isolated from an infected farm animal based on its annotated genome sequence. The
B
.
besnoiti
genome is highly syntenic with that of other CFA and also retains the capacity to encode a large majority of known and inferred factors essential for completing a sexual cycle in a yet unknown definitive host. This work introduces
Besnoitia besnoiti
as a new model for comparative biology of coccidian tissue cysts which can be readily obtained in high purity. This model provides a framework for addressing fundamental questions about the evolution of tissue cysts and the biology of this pharmacologically intractable infectious parasite stage. |
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Bibliography: | new_version ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Current address: Institute for Medical Engineering & Science and Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America Current address: EMBL Partner Institute for Genome Editing, Life Sciences Center–Vilnius University, Vilnius, Lithuania Current address: Infectious Disease and Microbiome Program, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America The authors have declared that no competing interests exist. |
ISSN: | 1553-7374 1553-7366 1553-7374 |
DOI: | 10.1371/journal.ppat.1010955 |