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dc.contributor.authorStetzner, Zachary W.
dc.contributor.authorLi, Dengfeng
dc.contributor.authorFeng, Wenchao
dc.contributor.authorLiu, Mengyao
dc.contributor.authorLiu, Guanghui
dc.contributor.authorWiley, James
dc.contributor.authorLei, Benfang
dc.date.accessioned2015-12-04T18:47:59Z
dc.date.available2015-12-04T18:47:59Z
dc.date.issued2015-06
dc.identifier.citationStetzner, Zachary W., Dengfeng Li, Wenchao Feng, Mengyao Liu, Guanghui Liu, James Wiley, and Benfang Lei. "Serotype M3 and M28 Group A Streptococci Have Distinct Capacities to Evade Neutrophil and TNF-α Responses and to Invade Soft Tissues ." PLoS ONE 10, no. 6 (June 2015): e0129417. DOI:https://dx.doi.org/10.1371/journal.pone.0129417.en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/9395
dc.description.abstractThe M3 Serotype of Group A Streptococcus (GAS) is one of the three most frequent serotypes associated with severe invasive GAS infections, such as necrotizing fasciitis, in the United States and other industrialized countries. The basis for this association and hypervirulence of invasive serotype M3 GAS is not fully understood. In this study, the sequenced serotype M3 strain, MGAS315, and serotype M28 strain, MGAS6180, were characterized in parallel to determine whether contemporary M3 GAS has a higher capacity to invade soft tissues than M28 GAS. In subcutaneous infection, MGAS315 invaded almost the whole skin, inhibited neutrophil recruitment and TNF-α production, and was lethal in subcutaneous infection of mice, whereas MGAS6180 did not invade skin, induced robust neutrophil infiltration and TNF-α production, and failed to kill mice. In contrast to MGAS6180, MGAS315 had covS G1370T mutation. Either replacement of the covS1370T gene with wild-type covS in MGAS315 chromosome or in trans expression of wild-type covS in MGAS315 reduced expression of CovRS-controlled virulence genes hasA, spyCEP, and sse by >10 fold. MGAS315 covSwt lost the capacity to extensively invade skin and to inhibit neutrophil recruitment and had attenuated virulence, indicating that the covS G1370T mutation critically contribute to the hypervirulence of MGAS315. Under the background of functional CovRS, MGAS315 covSwt still caused greater lesions than MGAS6180, and, consistently under the background of covS deletion, MGAS6180 ΔcovS caused smaller lesions than MGAS315 ΔcovS. Thus, contemporary invasive M3 GAS has a higher capacity to evade neutrophil and TNF-α responses and to invade soft tissue than M28 GAS and that this skin-invading capacity of M3 GAS is maximized by natural CovRS mutations. These findings enhance our understanding of the basis for the frequent association of M3 GAS with necrotizing fasciitis.en_US
dc.description.sponsorshipNIH AI095704; NIHAI097703;and GM110732 from the National Institutes of Health; USDA Animal Formula Fund; and the Montana State Agricultural Experimental Stationen_US
dc.rightsCCBY 4.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/legalcodeen_US
dc.titleSerotype M3 and M28 Group A Streptococci Have Distinct Capacities to Evade Neutrophil and TNF-α Responses and to Invade Soft Tissuesen_US
dc.typeArticleen_US
mus.citation.extentfirstpagee0129417en_US
mus.citation.issue6en_US
mus.citation.journaltitlePLoS ONEen_US
mus.citation.volume10en_US
mus.identifier.categoryChemical & Material Sciencesen_US
mus.identifier.categoryHealth & Medical Sciencesen_US
mus.identifier.doi10.1371/journal.pone.0129417en_US
mus.relation.collegeCollege of Agricultureen_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentMicrobiology & Immunology.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.data.thumbpage7en_US


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