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Role of arginine deiminase in thymic atrophy during experimental Streptococcus pyogenes infection
Expression of gene of arginine deiminase (AD) allows adaptation of Streptococcus pyogenes to adverse environmental conditions. AD activity can lead to L‐arginine deficiency in the host cells’ microenvironment. Bioavailability of L‐arginine is an important factor regulating the functions of the immun...
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Published in: | Scandinavian journal of immunology 2019-02, Vol.89 (2), p.e12734-n/a |
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creator | Starikova, Eleonora Alexandrovna Golovin, Alexander Stanislavovich Vasilyev, Kirill Alexandrovich Karaseva, Alena Borisovna Serebriakova, Maria Konstantinovna Sokolov, Alexey Victorovich Kudryavtsev, Igor Vladimirovich Burova, Larissa Alexandrovna Voynova, Irina Vitalyevna Suvorov, Alexander Nikolaevich Vasilyev, Vadim Borisovich Freidlin, Irina Solomonovna |
description | Expression of gene of arginine deiminase (AD) allows adaptation of Streptococcus pyogenes to adverse environmental conditions. AD activity can lead to L‐arginine deficiency in the host cells’ microenvironment. Bioavailability of L‐arginine is an important factor regulating the functions of the immune cells in mammals. By introducing a mutation into S pyogenes M46‐16, we obtained a strain with inactivated arcA/sagp gene (M49‐16 delArcA), deficient in AD. This allowed elucidating the function of AD in pathogenesis of streptococcal infection. The virulence of the parental and mutant strains was examined in a murine model of subcutaneous streptococcal infection. L‐arginine concentration in the plasma of mice infected with S pyogenes M49‐16 delArcA remained unchanged in course of the entire experiment. At the same time mice infected with S pyogenes M49‐16 demonstrated gradual diminution of L‐arginine concentration in the blood plasma, which might be due to the activity of streptococcal AD. Mice infected with S pyogenes M49‐16 delArcA demonstrated less intensive bacterial growth in the primary foci and less pronounced bacterial dissemination as compared with animals infected with the parental strain S pyogenes M46‐16. Similarly, thymus involution, alterations in apoptosis, thymocyte subsets and Treg cells differentiation were less pronounced in mice infected with S pyogenes M49‐16 delArcA than in those infected with the parental strain. The results obtained showed that S pyogenes M49‐16 delArcA, unable to produce AD, had reduced virulence in comparison with the parental S pyogenes M49‐16 strain. AD is an important factor for the realization of the pathogenic potential of streptococci. |
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AD activity can lead to L‐arginine deficiency in the host cells’ microenvironment. Bioavailability of L‐arginine is an important factor regulating the functions of the immune cells in mammals. By introducing a mutation into S pyogenes M46‐16, we obtained a strain with inactivated arcA/sagp gene (M49‐16 delArcA), deficient in AD. This allowed elucidating the function of AD in pathogenesis of streptococcal infection. The virulence of the parental and mutant strains was examined in a murine model of subcutaneous streptococcal infection. L‐arginine concentration in the plasma of mice infected with S pyogenes M49‐16 delArcA remained unchanged in course of the entire experiment. At the same time mice infected with S pyogenes M49‐16 demonstrated gradual diminution of L‐arginine concentration in the blood plasma, which might be due to the activity of streptococcal AD. Mice infected with S pyogenes M49‐16 delArcA demonstrated less intensive bacterial growth in the primary foci and less pronounced bacterial dissemination as compared with animals infected with the parental strain S pyogenes M46‐16. Similarly, thymus involution, alterations in apoptosis, thymocyte subsets and Treg cells differentiation were less pronounced in mice infected with S pyogenes M49‐16 delArcA than in those infected with the parental strain. The results obtained showed that S pyogenes M49‐16 delArcA, unable to produce AD, had reduced virulence in comparison with the parental S pyogenes M49‐16 strain. AD is an important factor for the realization of the pathogenic potential of streptococci.</description><identifier>ISSN: 0300-9475</identifier><identifier>EISSN: 1365-3083</identifier><identifier>DOI: 10.1111/sji.12734</identifier><identifier>PMID: 30471128</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Animal models ; Apoptosis ; Arginine ; Arginine deiminase ; Atrophy ; Bioavailability ; Blood levels ; Blood plasma ; Environmental conditions ; Infections ; Lymphocytes T ; Mice ; Rodents ; Streptococcus infections ; Streptococcus pyogenes ; Thymus ; Virulence</subject><ispartof>Scandinavian journal of immunology, 2019-02, Vol.89 (2), p.e12734-n/a</ispartof><rights>2018 The Foundation for the Scandinavian Journal of Immunology</rights><rights>2018 The Foundation for the Scandinavian Journal of Immunology.</rights><rights>Copyright © 2019 The Foundation for the Scandinavian Journal of Immunology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3884-b324df1617c2a0e17eb95780ad4fdaaec5612845748283334e566327288a87a03</citedby><cites>FETCH-LOGICAL-c3884-b324df1617c2a0e17eb95780ad4fdaaec5612845748283334e566327288a87a03</cites><orcidid>0000-0002-9687-7434</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30471128$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Starikova, Eleonora Alexandrovna</creatorcontrib><creatorcontrib>Golovin, Alexander Stanislavovich</creatorcontrib><creatorcontrib>Vasilyev, Kirill Alexandrovich</creatorcontrib><creatorcontrib>Karaseva, Alena Borisovna</creatorcontrib><creatorcontrib>Serebriakova, Maria Konstantinovna</creatorcontrib><creatorcontrib>Sokolov, Alexey Victorovich</creatorcontrib><creatorcontrib>Kudryavtsev, Igor Vladimirovich</creatorcontrib><creatorcontrib>Burova, Larissa Alexandrovna</creatorcontrib><creatorcontrib>Voynova, Irina Vitalyevna</creatorcontrib><creatorcontrib>Suvorov, Alexander Nikolaevich</creatorcontrib><creatorcontrib>Vasilyev, Vadim Borisovich</creatorcontrib><creatorcontrib>Freidlin, Irina Solomonovna</creatorcontrib><title>Role of arginine deiminase in thymic atrophy during experimental Streptococcus pyogenes infection</title><title>Scandinavian journal of immunology</title><addtitle>Scand J Immunol</addtitle><description>Expression of gene of arginine deiminase (AD) allows adaptation of Streptococcus pyogenes to adverse environmental conditions. AD activity can lead to L‐arginine deficiency in the host cells’ microenvironment. Bioavailability of L‐arginine is an important factor regulating the functions of the immune cells in mammals. By introducing a mutation into S pyogenes M46‐16, we obtained a strain with inactivated arcA/sagp gene (M49‐16 delArcA), deficient in AD. This allowed elucidating the function of AD in pathogenesis of streptococcal infection. The virulence of the parental and mutant strains was examined in a murine model of subcutaneous streptococcal infection. L‐arginine concentration in the plasma of mice infected with S pyogenes M49‐16 delArcA remained unchanged in course of the entire experiment. At the same time mice infected with S pyogenes M49‐16 demonstrated gradual diminution of L‐arginine concentration in the blood plasma, which might be due to the activity of streptococcal AD. Mice infected with S pyogenes M49‐16 delArcA demonstrated less intensive bacterial growth in the primary foci and less pronounced bacterial dissemination as compared with animals infected with the parental strain S pyogenes M46‐16. Similarly, thymus involution, alterations in apoptosis, thymocyte subsets and Treg cells differentiation were less pronounced in mice infected with S pyogenes M49‐16 delArcA than in those infected with the parental strain. The results obtained showed that S pyogenes M49‐16 delArcA, unable to produce AD, had reduced virulence in comparison with the parental S pyogenes M49‐16 strain. AD is an important factor for the realization of the pathogenic potential of streptococci.</description><subject>Animal models</subject><subject>Apoptosis</subject><subject>Arginine</subject><subject>Arginine deiminase</subject><subject>Atrophy</subject><subject>Bioavailability</subject><subject>Blood levels</subject><subject>Blood plasma</subject><subject>Environmental conditions</subject><subject>Infections</subject><subject>Lymphocytes T</subject><subject>Mice</subject><subject>Rodents</subject><subject>Streptococcus infections</subject><subject>Streptococcus pyogenes</subject><subject>Thymus</subject><subject>Virulence</subject><issn>0300-9475</issn><issn>1365-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAQhoMouq4e_AMS8KKHar7aZI-y-Ikg-HEu2XS6ZmmTmrRo_73RVQ-Cc5nLM-_MPAgdUHJKU53FlT2lTHKxgSaUF3nGieKbaEI4IdlMyHwH7ca4IoTyRG2jHU6EpJSpCdIPvgHsa6zD0jrrAFdgW-t0BGwd7l_G1hqs--C7lxFXQ7BuieG9g2BbcL1u8GMfoOu98cYMEXejX4KDmIZrML31bg9t1bqJsP_dp-j58uJpfp3d3V_dzM_vMsOVEtmCM1HVtKDSME2ASljMcqmIrkRdaQ0mL9LBIpdCMcU5F5AXRXqHKaWV1IRP0fE6twv-dYDYl62NBppGO_BDLBnlUhSzPBmYoqM_6MoPwaXrEiWZyNMelqiTNWWCjzFAXXbpaR3GkpLy03uZvJdf3hN7-J04LFqofskf0Qk4WwNvtoHx_6Ty8fZmHfkB4xqMGw</recordid><startdate>201902</startdate><enddate>201902</enddate><creator>Starikova, Eleonora Alexandrovna</creator><creator>Golovin, Alexander Stanislavovich</creator><creator>Vasilyev, Kirill Alexandrovich</creator><creator>Karaseva, Alena Borisovna</creator><creator>Serebriakova, Maria Konstantinovna</creator><creator>Sokolov, Alexey Victorovich</creator><creator>Kudryavtsev, Igor Vladimirovich</creator><creator>Burova, Larissa Alexandrovna</creator><creator>Voynova, Irina Vitalyevna</creator><creator>Suvorov, Alexander Nikolaevich</creator><creator>Vasilyev, Vadim Borisovich</creator><creator>Freidlin, Irina Solomonovna</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9687-7434</orcidid></search><sort><creationdate>201902</creationdate><title>Role of arginine deiminase in thymic atrophy during experimental Streptococcus pyogenes infection</title><author>Starikova, Eleonora Alexandrovna ; 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AD activity can lead to L‐arginine deficiency in the host cells’ microenvironment. Bioavailability of L‐arginine is an important factor regulating the functions of the immune cells in mammals. By introducing a mutation into S pyogenes M46‐16, we obtained a strain with inactivated arcA/sagp gene (M49‐16 delArcA), deficient in AD. This allowed elucidating the function of AD in pathogenesis of streptococcal infection. The virulence of the parental and mutant strains was examined in a murine model of subcutaneous streptococcal infection. L‐arginine concentration in the plasma of mice infected with S pyogenes M49‐16 delArcA remained unchanged in course of the entire experiment. At the same time mice infected with S pyogenes M49‐16 demonstrated gradual diminution of L‐arginine concentration in the blood plasma, which might be due to the activity of streptococcal AD. Mice infected with S pyogenes M49‐16 delArcA demonstrated less intensive bacterial growth in the primary foci and less pronounced bacterial dissemination as compared with animals infected with the parental strain S pyogenes M46‐16. Similarly, thymus involution, alterations in apoptosis, thymocyte subsets and Treg cells differentiation were less pronounced in mice infected with S pyogenes M49‐16 delArcA than in those infected with the parental strain. The results obtained showed that S pyogenes M49‐16 delArcA, unable to produce AD, had reduced virulence in comparison with the parental S pyogenes M49‐16 strain. AD is an important factor for the realization of the pathogenic potential of streptococci.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30471128</pmid><doi>10.1111/sji.12734</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-9687-7434</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animal models Apoptosis Arginine Arginine deiminase Atrophy Bioavailability Blood levels Blood plasma Environmental conditions Infections Lymphocytes T Mice Rodents Streptococcus infections Streptococcus pyogenes Thymus Virulence |
title | Role of arginine deiminase in thymic atrophy during experimental Streptococcus pyogenes infection |
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