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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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. |
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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><identifier>ISSN: 1462-5814</identifier><identifier>EISSN: 1462-5822</identifier><identifier>DOI: 10.1111/cmi.13275</identifier><identifier>PMID: 33006213</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Inc</publisher><subject>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</subject><ispartof>Cellular microbiology, 2021-02, Vol.23 (2), p.e13275-n/a</ispartof><rights>2020 John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons Ltd.</rights><rights>2021 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4435-70fd091e1268776c59cc492063488f810be0fe0c3867e84df080c3bf13d2722a3</citedby><cites>FETCH-LOGICAL-c4435-70fd091e1268776c59cc492063488f810be0fe0c3867e84df080c3bf13d2722a3</cites><orcidid>0000-0002-5560-806X ; 0000-0002-7504-4628</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcmi.13275$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcmi.13275$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,777,781,882,1412,1428,27905,27906,45555,45556,46390,46814</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33006213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>A novel tick protein supports integrity of gut peritrophic matrix impacting existence of gut microbiome and Lyme disease pathogens</title><title>Cellular microbiology</title><addtitle>Cell Microbiol</addtitle><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.</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 & 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 & 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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