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A novel tick protein supports integrity of gut peritrophic matrix impacting existence of gut microbiome and Lyme disease pathogens.

Authors :
Yang, Xiuli
Koči, Juraj
Smith, Alexis A.
Zhuang, Xuran
Sharma, Kavita
Dutta, Shraboni
Rana, Vipin S.
Kitsou, Chrysoula
Yas, Ozlem B.
Mongodin, Emmanuel F.
Pal, Utpal
Source :
Cellular Microbiology. Feb2021, Vol. 23 Issue 2, p1-12. 12p.
Publication Year :
2021

Abstract

The peritrophic matrix (PM) is an acellular membrane that covers the gut epithelium in arthropods and physically separates it from the lumen. The structure is thought to play an important role in tick biology. The PM is also known to impact the persistence of tick‐borne pathogens like Borrelia burgdorferi, although limited information is available about its molecular constituents or their biological significance. Herein, we characterise a novel PM‐associated gut protein in Ixodes scapularis ticks, annotated as Peritrophic Membrane Chitin Binding Protein (PM_CBP), for its role in the integrity and function of the matrix. The PM_CBP displays homology to the chitin deacetylase metalloenzyme, shows upregulation during tick feeding, and is localized at the luminal surface of the gut epithelium. The structural integrity of the PM was impaired both by the knock down of PM_CBP expression via RNA interference and by treatment with anti‐PM_CBP antibodies, as revealed by its electron microscopic appearance. Additionally, the duration of tick engorgement on mice and the passage of experimentally‐inoculated fluorescent dextran molecules across the PM are affected by the knock down of PM_CBP expression. The transfer of anti‐PM_CBP antibodies into the tick gut impacted the overall composition of the resident microbiome, and also influenced B. burgdorferi acquisition in ticks and its transmission to mice. Taken together, these data highlight the biological significance of the Ixodes PM and suggest that the targeting of its molecular constituents may contribute to the development of novel interventions against tick‐borne infections. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14625814
Volume :
23
Issue :
2
Database :
Academic Search Index
Journal :
Cellular Microbiology
Publication Type :
Academic Journal
Accession number :
148184721
Full Text :
https://doi.org/10.1111/cmi.13275