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For: Goyette-Desjardins G, Auger JP, Xu J, Segura M, Gottschalk M. Streptococcus suis, an important pig pathogen and emerging zoonotic agent-an update on the worldwide distribution based on serotyping and sequence typing. Emerg Microbes Infect 2014;3:e45. [PMID: 26038745 DOI: 10.1038/emi.2014.45] [Cited by in Crossref: 311] [Cited by in F6Publishing: 301] [Article Influence: 38.9] [Reference Citation Analysis]
Number Citing Articles
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10 Zhong X, Ma J, Bai Q, Zhu Y, Zhang Y, Gu Q, Pan Z, Liu G, Wu Z, Yao H. Identification of the RNA-binding domain-containing protein RbpA that acts as a global regulator of the pathogenicity of Streptococcus suis serotype 2. Virulence 2022;13:1304-14. [PMID: 35903019 DOI: 10.1080/21505594.2022.2103233] [Reference Citation Analysis]
11 Songsungthong W, Prasopporn S, Bohan L, Srimanote P, Leartsakulpanich U, Yongkiettrakul S. A novel bicyclic 2,4-diaminopyrimidine inhibitor of Streptococcus suis dihydrofolate reductase. PeerJ 2021;9:e10743. [PMID: 33604179 DOI: 10.7717/peerj.10743] [Reference Citation Analysis]
12 Wang X, Sun J, Bian C, Wang J, Liang Z, Shen Y, Yao H, Huang J, Wang L, Zheng H, Wu Z. The population structure, antimicrobial resistance, and pathogenicity of Streptococcus suis cps31. Vet Microbiol 2021;259:109149. [PMID: 34147764 DOI: 10.1016/j.vetmic.2021.109149] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Auger JP, Gottschalk M. The Streptococcus suis factor H-binding protein: A key to unlocking the blood-brain barrier and access the central nervous system? Virulence 2017;8:1081-4. [PMID: 28622084 DOI: 10.1080/21505594.2017.1342027] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.6] [Reference Citation Analysis]
14 Fernández-Aguilar X, Gottschalk M, Aragon V, Càmara J, Ardanuy C, Velarde R, Galofré-Milà N, Castillo-Contreras R, López-Olvera JR, Mentaberre G, Colom-Cadena A, Lavín S, Cabezón O. Urban Wild Boars and Risk for Zoonotic Streptococcus suis, Spain. Emerg Infect Dis 2018;24:1083-6. [PMID: 29774831 DOI: 10.3201/eid2406.171271] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 4.3] [Reference Citation Analysis]
15 Ni H, Fan W, Li C, Wu Q, Hou H, Hu D, Zheng F, Zhu X, Wang C, Cao X, Shao ZQ, Pan X. Streptococcus suis DivIVA Protein Is a Substrate of Ser/Thr Kinase STK and Involved in Cell Division Regulation. Front Cell Infect Microbiol 2018;8:85. [PMID: 29616196 DOI: 10.3389/fcimb.2018.00085] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 2.8] [Reference Citation Analysis]
16 Lacouture S, Okura M, Takamatsu D, Corsaut L, Gottschalk M. Development of a mismatch amplification mutation assay to correctly serotype isolates of Streptococcus suis serotypes 1, 2, 1/2, and 14. J Vet Diagn Invest 2020;32:490-4. [PMID: 32306861 DOI: 10.1177/1040638720915869] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
17 Zhang Y, Zong B, Wang X, Zhu Y, Hu L, Li P, Zhang A, Chen H, Liu M, Tan C. Fisetin Lowers Streptococcus suis serotype 2 Pathogenicity in Mice by Inhibiting the Hemolytic Activity of Suilysin. Front Microbiol 2018;9:1723. [PMID: 30105012 DOI: 10.3389/fmicb.2018.01723] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 2.5] [Reference Citation Analysis]
18 Kuttel MM. Comparative Molecular Modelling of Capsular Polysaccharide Conformations in Streptococcus suis Serotypes 1, 2, 1/2 and 14 Identifies Common Epitopes for Antibody Binding. Front Mol Biosci 2022;9:830854. [DOI: 10.3389/fmolb.2022.830854] [Reference Citation Analysis]
19 Gómez-Gascón L, Cardoso-Toset F, Tarradas C, Gómez-Laguna J, Maldonado A, Nielsen J, Olaya-Abril A, Rodríguez-Ortega MJ, Luque I. Characterization of the immune response and evaluation of the protective capacity of rSsnA against Streptococcus suis infection in pigs. Comp Immunol Microbiol Infect Dis 2016;47:52-9. [PMID: 27477507 DOI: 10.1016/j.cimid.2016.06.001] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
20 Ferrando ML, Gussak A, Mentink S, Gutierrez MF, van Baarlen P, Wells JM. Active Human and Porcine Serum Induce Competence for Genetic Transformation in the Emerging Zoonotic Pathogen Streptococcus suis. Pathogens 2021;10:156. [PMID: 33546136 DOI: 10.3390/pathogens10020156] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Jia M, Wei M, Zhang Y, Zheng C. Transcriptomic Analysis of Streptococcus suis in Response to Ferrous Iron and Cobalt Toxicity. Genes (Basel) 2020;11:E1035. [PMID: 32887434 DOI: 10.3390/genes11091035] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
22 Okura M, Auger JP, Shibahara T, Goyette-Desjardins G, Van Calsteren MR, Maruyama F, Kawai M, Osaki M, Segura M, Gottschalk M, Takamatsu D. Capsular polysaccharide switching in Streptococcus suis modulates host cell interactions and virulence. Sci Rep 2021;11:6513. [PMID: 33753801 DOI: 10.1038/s41598-021-85882-3] [Reference Citation Analysis]
23 Auger JP, Payen S, Roy D, Dumesnil A, Segura M, Gottschalk M. Interactions of Streptococcus suis serotype 9 with host cells and role of the capsular polysaccharide: Comparison with serotypes 2 and 14. PLoS One 2019;14:e0223864. [PMID: 31600314 DOI: 10.1371/journal.pone.0223864] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
24 Vinogradov E, Goyette-Desjardins G, Okura M, Takamatsu D, Gottschalk M, Segura M. Structure determination of Streptococcus suis serotype 9 capsular polysaccharide and assignment of functions of the cps locus genes involved in its biosynthesis. Carbohydr Res 2016;433:25-30. [PMID: 27423880 DOI: 10.1016/j.carres.2016.07.005] [Cited by in Crossref: 16] [Cited by in F6Publishing: 12] [Article Influence: 2.7] [Reference Citation Analysis]
25 Dekker N, Daemen I, Verstappen K, de Greeff A, Smith H, Duim B. Simultaneous Quantification and Differentiation of Streptococcus suis Serotypes 2 and 9 by Quantitative Real-Time PCR, Evaluated in Tonsillar and Nasal Samples of Pigs. Pathogens 2016;5:E46. [PMID: 27376336 DOI: 10.3390/pathogens5030046] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
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27 Liang Z, Wu H, Bian C, Chen H, Shen Y, Gao X, Ma J, Yao H, Wang L, Wu Z. The antimicrobial systems of Streptococcus suis promote niche competition in pig tonsils. Virulence 2022;13:781-93. [PMID: 35481413 DOI: 10.1080/21505594.2022.2069390] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
28 Zheng C, Wei M, Qiu J, Li J. A Markerless Gene Deletion System in Streptococcus suis by Using the Copper-Inducible Vibrio parahaemolyticus YoeB Toxin as a Counterselectable Marker. Microorganisms 2021;9:1095. [PMID: 34069706 DOI: 10.3390/microorganisms9051095] [Reference Citation Analysis]
29 Willemse N, van der Ende A, Schultsz C. Reinfection with Streptococcus suis analysed by whole genome sequencing. Zoonoses Public Health 2019;66:179-83. [PMID: 30306727 DOI: 10.1111/zph.12528] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
30 Willemse N, Schultsz C. Distribution of Type I Restriction-Modification Systems in Streptococcus suis: An Outlook. Pathogens 2016;5:E62. [PMID: 27869755 DOI: 10.3390/pathogens5040062] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
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33 Neila-Ibáñez C, Brogaard L, Pailler-García L, Martínez J, Segalés J, Segura M, Heegaard PMH, Aragon V. Piglet innate immune response to Streptococcus suis colonization is modulated by the virulence of the strain. Vet Res 2021;52:145. [PMID: 34924012 DOI: 10.1186/s13567-021-01013-w] [Reference Citation Analysis]
34 O'Dea MA, Laird T, Abraham R, Jordan D, Lugsomya K, Fitt L, Gottschalk M, Truswell A, Abraham S. Examination of Australian Streptococcus suis isolates from clinically affected pigs in a global context and the genomic characterisation of ST1 as a predictor of virulence. Vet Microbiol 2018;226:31-40. [PMID: 30389041 DOI: 10.1016/j.vetmic.2018.10.010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
35 Kerdsin A, Akeda Y, Takeuchi D, Dejsirilert S, Gottschalk M, Oishi K. Genotypic diversity of Streptococcus suis strains isolated from humans in Thailand. Eur J Clin Microbiol Infect Dis 2018;37:917-25. [PMID: 29417311 DOI: 10.1007/s10096-018-3208-8] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
36 Li Q, Lv Y, Li YA, Du Y, Guo W, Chu D, Wang X, Wang S, Shi H. Live attenuated Salmonella enterica serovar Choleraesuis vector delivering a conserved surface protein enolase induces high and broad protection against Streptococcus suis serotypes 2, 7, and 9 in mice. Vaccine 2020;38:6904-13. [PMID: 32907758 DOI: 10.1016/j.vaccine.2020.08.062] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
37 Liu H, Hou C, Wang G, Jia H, Yu H, Zeng X, Thacker PA, Zhang G, Qiao S. Lactobacillus reuteri I5007 Modulates Intestinal Host Defense Peptide Expression in the Model of IPEC-J2 Cells and Neonatal Piglets. Nutrients 2017;9:E559. [PMID: 28561758 DOI: 10.3390/nu9060559] [Cited by in Crossref: 36] [Cited by in F6Publishing: 33] [Article Influence: 7.2] [Reference Citation Analysis]
38 Auger JP, Benoit-Biancamano MO, Bédard C, Segura M, Gottschalk M. Differential role of MyD88 signaling in Streptococcus suis serotype 2-induced systemic and central nervous system diseases. Int Immunol 2019;31:697-714. [PMID: 30944920 DOI: 10.1093/intimm/dxz033] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
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40 Payen S, Roy D, Boa A, Okura M, Auger JP, Segura M, Gottschalk M. Role of Maturation of Lipoproteins in the Pathogenesis of the Infection Caused by Streptococcus suis Serotype 2. Microorganisms 2021;9:2386. [PMID: 34835511 DOI: 10.3390/microorganisms9112386] [Reference Citation Analysis]
41 Chuzeville S, Auger JP, Dumesnil A, Roy D, Lacouture S, Fittipaldi N, Grenier D, Gottschalk M. Serotype-specific role of antigen I/II in the initial steps of the pathogenesis of the infection caused by Streptococcus suis. Vet Res 2017;48:39. [PMID: 28705175 DOI: 10.1186/s13567-017-0443-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
42 Xia X, Wang L, Shen Z, Qin W, Hu J, Jiang S, Li S. Development of an Indirect Dot-PPA-ELISA using glutamate dehydrogenase as a diagnostic antigen for the rapid and specific detection of Streptococcus suis and its application to clinical specimens. Antonie van Leeuwenhoek 2017;110:585-92. [DOI: 10.1007/s10482-016-0825-z] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
43 Xie F, Zan Y, Zhang Y, Zheng N, Yan Q, Zhang W, Zhang H, Jin M, Chen F, Zhang X, Liu S. The cysteine protease ApdS from Streptococcus suis promotes evasion of innate immune defenses by cleaving the antimicrobial peptide cathelicidin LL-37. J Biol Chem 2019;294:17962-77. [PMID: 31619521 DOI: 10.1074/jbc.RA119.009441] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
44 Dechêne-Tempier M, Marois-Créhan C, Libante V, Jouy E, Leblond-Bourget N, Payot S. Update on the Mechanisms of Antibiotic Resistance and the Mobile Resistome in the Emerging Zoonotic Pathogen Streptococcus suis. Microorganisms 2021;9:1765. [PMID: 34442843 DOI: 10.3390/microorganisms9081765] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
45 Rayanakorn A, Goh BH, Lee LH, Khan TM, Saokaew S. Risk factors for Streptococcus suis infection: A systematic review and meta-analysis. Sci Rep 2018;8:13358. [PMID: 30190575 DOI: 10.1038/s41598-018-31598-w] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 4.8] [Reference Citation Analysis]
46 Bai Q, Ma J, Zhang Z, Zhong X, Pan Z, Zhu Y, Zhang Y, Wu Z, Liu G, Yao H. YSIRK-G/S-directed translocation is required for Streptococcus suis to deliver diverse cell wall anchoring effectors contributing to bacterial pathogenicity. Virulence 2020;11:1539-56. [PMID: 33138686 DOI: 10.1080/21505594.2020.1838740] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
47 Ruzauskas M, Bartkiene E, Stankevicius A, Bernatoniene J, Zadeike D, Lele V, Starkute V, Zavistanaviciute P, Grigas J, Zokaityte E, Pautienius A, Juodeikiene G, Jakstas V. The Influence of Essential Oils on Gut Microbial Profiles in Pigs. Animals (Basel) 2020;10:E1734. [PMID: 32987688 DOI: 10.3390/ani10101734] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
48 Meurer M, de Buhr N, Unger LM, Bonilla MC, Seele J, Nau R, Baums CG, Gutsmann T, Schwarz S, von Köckritz-Blickwede M. Comparing Cathelicidin Susceptibility of the Meningitis Pathogens Streptococcus suis and Escherichia coli in Culture Medium in Contrast to Porcine or Human Cerebrospinal Fluid. Front Microbiol 2019;10:2911. [PMID: 31993024 DOI: 10.3389/fmicb.2019.02911] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
49 van der Wal FJ, Achterberg RP, van Solt-Smits C, Bergervoet JHW, de Weerdt M, Wisselink HJ. Exploring target-specific primer extension in combination with a bead-based suspension array for multiplexed detection and typing using Streptococcus suis as a model pathogen. J Vet Diagn Invest 2018;30:71-7. [PMID: 28980519 DOI: 10.1177/1040638717730384] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
50 Yamada R, Tien LHT, Arai S, Tohya M, Ishida-Kuroki K, Nomoto R, Kim H, Suzuki E, Osawa R, Watanabe T, Sekizaki T. Development of PCR for identifying Streptococcus parasuis, a close relative of Streptococcus suis. J Vet Med Sci 2018;80:1101-7. [PMID: 29877313 DOI: 10.1292/jvms.18-0083] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
51 Han L, Fu L, Peng Y, Zhang A. Triggering Receptor Expressed on Myeloid Cells-1 Signaling: Protective and Pathogenic Roles on Streptococcal Toxic-Shock-Like Syndrome Caused by Streptococcus suis. Front Immunol 2018;9:577. [PMID: 29619033 DOI: 10.3389/fimmu.2018.00577] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
52 Du F, Lv X, Duan D, Wang L, Huang J. Characterization of a Linezolid- and Vancomycin-Resistant Streptococcus suis Isolate That Harbors optrA and vanG Operons. Front Microbiol 2019;10:2026. [PMID: 31551963 DOI: 10.3389/fmicb.2019.02026] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 4.7] [Reference Citation Analysis]
53 Giang E, Hetman BM, Sargeant JM, Poljak Z, Greer AL. Examining the Effect of Host Recruitment Rates on the Transmission of Streptococcus suis in Nursery Swine Populations. Pathogens 2020;9:E174. [PMID: 32121513 DOI: 10.3390/pathogens9030174] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
54 Gao G, Wei D, Li G, Chen P, Wu L, Liu S, Zhang Y. Highly Effective Markerless Genetic Manipulation of Streptococcus suis Using a Mutated PheS-Based Counterselectable Marker. Front Microbiol 2022;13:947821. [DOI: 10.3389/fmicb.2022.947821] [Reference Citation Analysis]
55 Li Q, Fei X, Zhang Y, Guo G, Shi H, Zhang W. The biological role of MutT in the pathogenesis of the zoonotic pathogen Streptococcus suis serotype 2. Virulence 2021;12:1538-49. [PMID: 34077309 DOI: 10.1080/21505594.2021.1936770] [Reference Citation Analysis]
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59 Raberahona M, Rasoanandrasana S, Rahajamanana VL, Ranaivo-Rabetokotany F, Andriananja V, Rakotomalala FA, Randria MJD, Rakotovao L, Marois-Créhan C, Tocqueville V, Touzain F, Rakoto-Andrianarivelo M. Novel Streptococcus suis Sequence Type 834 among Humans, Madagascar. Emerg Infect Dis 2018;24:391-2. [PMID: 29350165 DOI: 10.3201/eid2402.171138] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
60 Gu Q, He P, Wang D, Ma J, Zhong X, Zhu Y, Zhang Y, Bai Q, Pan Z, Yao H. An Auto-Regulating Type II Toxin-Antitoxin System Modulates Drug Resistance and Virulence in Streptococcus suis. Front Microbiol 2021;12:671706. [PMID: 34475853 DOI: 10.3389/fmicb.2021.671706] [Reference Citation Analysis]
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