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

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 burgd...

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Veröffentlicht in:Cellular microbiology 2021-02, Vol.23 (2), p.e13275-n/a
Hauptverfasser: 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
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container_issue 2
container_start_page e13275
container_title Cellular microbiology
container_volume 23
creator 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
description 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. The peritrophic membrane (PM) in tick gut covers the epithelial cells (EC) and physically separates them from the lumen. This study identified a PM‐associated protein in Ixodes ticks, called Peritrophic Membrane Chitin Binding Protein (PM_CBP), for its role in the integrity and function of the membrane. The normal PM integrity (upper image) can be impaired by treatment with anti‐PM_CBP antibodies (bottom image), as revealed by its reduced thickness seen under an electron microscope, ultimately impacting existence of gut microbiome and Lyme disease pathogens.
doi_str_mv 10.1111/cmi.13275
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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. The peritrophic membrane (PM) in tick gut covers the epithelial cells (EC) and physically separates them from the lumen. This study identified a PM‐associated protein in Ixodes ticks, called Peritrophic Membrane Chitin Binding Protein (PM_CBP), for its role in the integrity and function of the membrane. 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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. The peritrophic membrane (PM) in tick gut covers the epithelial cells (EC) and physically separates them from the lumen. This study identified a PM‐associated protein in Ixodes ticks, called Peritrophic Membrane Chitin Binding Protein (PM_CBP), for its role in the integrity and function of the membrane. The normal PM integrity (upper image) can be impaired by treatment with anti‐PM_CBP antibodies (bottom image), as revealed by its reduced thickness seen under an electron microscope, ultimately impacting existence of gut microbiome and Lyme disease pathogens.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Arachnids</subject><subject>Arthropod Proteins - metabolism</subject><subject>Arthropods</subject><subject>Borrelia burgdorferi - pathogenicity</subject><subject>Borrelia burgdorferi - physiology</subject><subject>Carrier Proteins - metabolism</subject><subject>Chitin</subject><subject>Chitin - metabolism</subject><subject>Chitin deacetylase</subject><subject>Constituents</subject><subject>Dextran</subject><subject>Dextrans</subject><subject>DNA, Bacterial</subject><subject>Engorgement</subject><subject>Epithelium</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Gastrointestinal Microbiome</subject><subject>Gene expression</subject><subject>Gene Knockdown Techniques</subject><subject>Homology</subject><subject>Host-Pathogen Interactions</subject><subject>infection</subject><subject>Intestinal microflora</subject><subject>Intestinal Mucosa - microbiology</subject><subject>Ixodes - metabolism</subject><subject>Ixodes - microbiology</subject><subject>Lyme disease</subject><subject>Lyme Disease - microbiology</subject><subject>Membrane proteins</subject><subject>Membranes</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>microbial‐cell interaction</subject><subject>Microbiomes</subject><subject>Pathogens</subject><subject>Peritrophic membrane</subject><subject>Protein Binding</subject><subject>Proteins</subject><subject>RNA Interference</subject><subject>RNA, Ribosomal, 16S</subject><subject>RNA-mediated interference</subject><subject>Structural integrity</subject><subject>Ticks</subject><subject>vaccines</subject><subject>Vector-borne diseases</subject><issn>1462-5814</issn><issn>1462-5822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1v1DAQhi0EoqVw4A8gS1zoYVt_JXYuSNWKQqWtuMDZ8jqTrEtiB9tpu9f-8rpsuwKk-uIZ-dGjGb8IvafkhJZzakd3QjmT1Qt0SEXNFpVi7OW-puIAvUnpihBaS0pfowPOCakZ5Yfo7gz7cA0Dzs7-wlMMGZzHaZ6mEHPCzmfoo8tbHDrczxlPULoYpo2zeDQ5ulvsxsnY7HyP4dalDN7CEz06G8PahRGw8S1ebUvRugQmAZ5M3oQefHqLXnVmSPDu8T5CP8-__Fh-W6y-f71Ynq0WVgheLSTpWtJQoKxWUta2aqwVDSM1F0p1ipI1kA6I5aqWoETbEVWadUd5yyRjhh-hzzvvNK9HaC34HM2gp-hGE7c6GKf_ffFuo_twrRvCFZF1EXx6FMTwe4aU9eiShWEwHsKcNBNCCUoZEQX9-B96Feboy3qFkkpVjDYPwuMdVX4ppQjdfhhK9EOyuiSr_yRb2A9_T78nn6IswOkOuHEDbJ836eXlxU55D1c8r38</recordid><startdate>202102</startdate><enddate>202102</enddate><creator>Yang, Xiuli</creator><creator>Koči, Juraj</creator><creator>Smith, Alexis A.</creator><creator>Zhuang, Xuran</creator><creator>Sharma, Kavita</creator><creator>Dutta, Shraboni</creator><creator>Rana, Vipin S.</creator><creator>Kitsou, Chrysoula</creator><creator>Yas, Ozlem B.</creator><creator>Mongodin, Emmanuel F.</creator><creator>Pal, Utpal</creator><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5560-806X</orcidid><orcidid>https://orcid.org/0000-0002-7504-4628</orcidid></search><sort><creationdate>202102</creationdate><title>A novel tick protein supports integrity of gut peritrophic matrix impacting existence of gut microbiome and Lyme disease pathogens</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4435-70fd091e1268776c59cc492063488f810be0fe0c3867e84df080c3bf13d2722a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Arachnids</topic><topic>Arthropod Proteins - metabolism</topic><topic>Arthropods</topic><topic>Borrelia burgdorferi - pathogenicity</topic><topic>Borrelia burgdorferi - physiology</topic><topic>Carrier Proteins - metabolism</topic><topic>Chitin</topic><topic>Chitin - metabolism</topic><topic>Chitin deacetylase</topic><topic>Constituents</topic><topic>Dextran</topic><topic>Dextrans</topic><topic>DNA, Bacterial</topic><topic>Engorgement</topic><topic>Epithelium</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Gastrointestinal Microbiome</topic><topic>Gene expression</topic><topic>Gene Knockdown Techniques</topic><topic>Homology</topic><topic>Host-Pathogen Interactions</topic><topic>infection</topic><topic>Intestinal microflora</topic><topic>Intestinal Mucosa - microbiology</topic><topic>Ixodes - metabolism</topic><topic>Ixodes - microbiology</topic><topic>Lyme disease</topic><topic>Lyme Disease - microbiology</topic><topic>Membrane proteins</topic><topic>Membranes</topic><topic>Mice</topic><topic>Mice, Inbred C3H</topic><topic>microbial‐cell interaction</topic><topic>Microbiomes</topic><topic>Pathogens</topic><topic>Peritrophic membrane</topic><topic>Protein Binding</topic><topic>Proteins</topic><topic>RNA Interference</topic><topic>RNA, Ribosomal, 16S</topic><topic>RNA-mediated interference</topic><topic>Structural integrity</topic><topic>Ticks</topic><topic>vaccines</topic><topic>Vector-borne diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Xiuli</creatorcontrib><creatorcontrib>Koči, Juraj</creatorcontrib><creatorcontrib>Smith, Alexis A.</creatorcontrib><creatorcontrib>Zhuang, Xuran</creatorcontrib><creatorcontrib>Sharma, Kavita</creatorcontrib><creatorcontrib>Dutta, Shraboni</creatorcontrib><creatorcontrib>Rana, Vipin S.</creatorcontrib><creatorcontrib>Kitsou, Chrysoula</creatorcontrib><creatorcontrib>Yas, Ozlem B.</creatorcontrib><creatorcontrib>Mongodin, Emmanuel F.</creatorcontrib><creatorcontrib>Pal, Utpal</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cellular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Xiuli</au><au>Koči, Juraj</au><au>Smith, Alexis A.</au><au>Zhuang, Xuran</au><au>Sharma, Kavita</au><au>Dutta, Shraboni</au><au>Rana, Vipin S.</au><au>Kitsou, Chrysoula</au><au>Yas, Ozlem B.</au><au>Mongodin, Emmanuel F.</au><au>Pal, Utpal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A novel tick protein supports integrity of gut peritrophic matrix impacting existence of gut microbiome and Lyme disease pathogens</atitle><jtitle>Cellular microbiology</jtitle><addtitle>Cell Microbiol</addtitle><date>2021-02</date><risdate>2021</risdate><volume>23</volume><issue>2</issue><spage>e13275</spage><epage>n/a</epage><pages>e13275-n/a</pages><issn>1462-5814</issn><eissn>1462-5822</eissn><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. The peritrophic membrane (PM) in tick gut covers the epithelial cells (EC) and physically separates them from the lumen. This study identified a PM‐associated protein in Ixodes ticks, called Peritrophic Membrane Chitin Binding Protein (PM_CBP), for its role in the integrity and function of the membrane. The normal PM integrity (upper image) can be impaired by treatment with anti‐PM_CBP antibodies (bottom image), as revealed by its reduced thickness seen under an electron microscope, ultimately impacting existence of gut microbiome and Lyme disease pathogens.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>33006213</pmid><doi>10.1111/cmi.13275</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-5560-806X</orcidid><orcidid>https://orcid.org/0000-0002-7504-4628</orcidid><oa>free_for_read</oa></addata></record>
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subjects Animals
Antibodies
Arachnids
Arthropod Proteins - metabolism
Arthropods
Borrelia burgdorferi - pathogenicity
Borrelia burgdorferi - physiology
Carrier Proteins - metabolism
Chitin
Chitin - metabolism
Chitin deacetylase
Constituents
Dextran
Dextrans
DNA, Bacterial
Engorgement
Epithelium
Female
Fluorescence
Gastrointestinal Microbiome
Gene expression
Gene Knockdown Techniques
Homology
Host-Pathogen Interactions
infection
Intestinal microflora
Intestinal Mucosa - microbiology
Ixodes - metabolism
Ixodes - microbiology
Lyme disease
Lyme Disease - microbiology
Membrane proteins
Membranes
Mice
Mice, Inbred C3H
microbial‐cell interaction
Microbiomes
Pathogens
Peritrophic membrane
Protein Binding
Proteins
RNA Interference
RNA, Ribosomal, 16S
RNA-mediated interference
Structural integrity
Ticks
vaccines
Vector-borne diseases
title A novel tick protein supports integrity of gut peritrophic matrix impacting existence of gut microbiome and Lyme disease pathogens
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