Acker HV, Dijck PV, Coenye T (2014) Molecular mechanisms of antimicrobial tolerance and resistance in bacterial and fungal biofilms. Trends Microbiol 22(6):326–333. https://doi.org/10.1016/j.tim.2014.02.001
CAS
Article
PubMed
Google Scholar
Bazire A, Shioya K, Soumsoutéra E, Bouffartigues E, Ryder C, Guentasdombrowsky L, Hémery G, Linossier I, Chevalier S, Wozniak DJ (2010) The sigma factor Algu plays a key role in formation of robust biofilms by nonmucoid Pseudomonas aeruginosa. J Bacteriol 192(12):3001–3010. https://doi.org/10.1128/JB.01633-09
CAS
Article
PubMed
PubMed Central
Google Scholar
Bonifait L, Grignon L, Grenier D (2008) Fibrinogen induces biofilm formation by Streptococcus suis and enhances its antibiotic resistance. Appl Environ Microbiol 74(15):4969–4972. https://doi.org/10.1128/AEM.00558-08
CAS
Article
PubMed
PubMed Central
Google Scholar
Bonifait L, Gottschalk M, Grenier D (2010) Cell surface characteristics of nontypeable isolates of Streptococcus suis. FEMS Microbiol Lett 311(2):160–166. https://doi.org/10.1128/AEM.00558-08
CAS
Article
PubMed
Google Scholar
Choi KS, Veeraragouda Y, Cho KM, Lee SO, Jo GR, Cho K, Lee K (2007) Effect of Gacs and Gac a mutations on colony architecture, surface motility, biofilm formation and chemical toxicity in Pseudomonas Sp. Kl28. J Microbiol 45(6):492–498
CAS
PubMed
Google Scholar
Chuzeville S, Auger JP, Dumesnil A, Roy D, Lacouture S, Fittipaldi N, Grenier D, Gottschalk M (2017) Serotype-specific role of antigen I/Ii in the initial steps of the pathogenesis of the infection caused by Streptococcus suis. Vet Res 48(1):39. https://doi.org/10.1186/s13567-017-0443-4
CAS
Article
PubMed
PubMed Central
Google Scholar
Ciofu O, Tolker-Nielsen T, Jensen PØ, Wang H, Høiby N (2015) Antimicrobial resistance, respiratory tract infections and role of biofilms in lung infections in cystic fibrosis patients. Adv Drug Deliv Rev 85:7–23. https://doi.org/10.1016/j.addr.2014.11.017
CAS
Article
PubMed
Google Scholar
Coenye T (2010) Social interactions in the Burkholderia cepacia complex: biofilms and quorum sensing. Future Microbiol 5(7):1087–1099. https://doi.org/10.2217/fmb.10.68
CAS
Article
PubMed
Google Scholar
Ding WY, Li YH, Lian H, Ai XY, Zhao YL, Yang YB, Han Q, Liu X, Chen XY, He Z (2017) Sub-minimum inhibitory concentrations of rhubarb water extracts inhibit Streptococcus suis biofilm formation. Front Pharmacol 8:425. https://doi.org/10.3389/fphar.2017.00425
Article
PubMed
PubMed Central
Google Scholar
Ding W, Sun J, Lian H, Xu C, Liu X, Zheng S, Zhang D, Han X, Liu Y, Chen X (2018) The influence of shuttle-shape Emodin nanoparticles on the Streptococcus suis biofilm. Front Pharmacol 9:227. https://doi.org/10.3389/fphar.2018.00227
Article
PubMed
PubMed Central
Google Scholar
Donlan RM, Costerton JW (2002) Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev 15(2):167–193. https://doi.org/10.1128/CMR.15.2.167-193.2002
CAS
Article
PubMed
PubMed Central
Google Scholar
Du B, Ji W, An H, Shi Y, Huang Q, Cheng Y, Fu Q, Wang H, Yan Y, Sun J (2014) Functional analysis of C-Di-amp phosphodiesterase, Gdpp, in Streptococcus suis serotype 2. Microbiol Res 169(9–10):749–758. https://doi.org/10.1016/j.micres.2014.01.002
CAS
Article
PubMed
Google Scholar
Duguid IG, Evans E, Brown MR, Gilbert P (1992) Effect of biofilm culture upon the susceptibility of Staphylococcus epidermidis to tobramycin. J Antimicrob Chemother 30(6):803–810. https://doi.org/10.1093/jac/30.6.803
CAS
Article
PubMed
Google Scholar
Espinosa I, Báez M, Lobo E, Martínez S, Gottschalk M (2016) Antimicrobial activity of penicillin G and N-acetylcystein on planktonic and sessile cells of Streptococcus suis. Polish J Microbiol 65(1):105–109
Article
Google Scholar
Evans DJ, Allison DG, Brown MR, Gilbert P (1991) Susceptibility of Pseudomonas aeruginosa and Escherichia coli biofilms towards ciprofloxacin: effect of specific growth rate. J Antimicrob Chemother 27(2):177–184. https://doi.org/10.1093/jac/27.2.177
CAS
Article
PubMed
Google Scholar
Fittipaldi N, Segura M, Grenier D, Gottschalk M (2012) Virulence factors involved in the pathogenesis of the infection caused by the swine pathogen and zoonotic agent Streptococcus suis. Future Microbiol 7(2):259–279. https://doi.org/10.2217/fmb.11.149
CAS
Article
PubMed
Google Scholar
Gao LF, Chen JQ, Sheng ZL, Liu XL, Wei SG, Zhang CL, Fang L, Li YH (2015) Screening of the effective parts of Syringa oblate Lindl leaf to intervene the in vitro biofilm formation of Streptococcus suis. Heilongjiang Anim Sci Vet Med (13):189–191
Ghadam P, Akhlaghi F, Abdi Ali A (2017) One-step purification and characterization of alginate lyase from a clinical Pseudomonas aeruginosa with destructive activity on bacterial biofilm. Iranian J Basic Med Sci 20(5):467–473. https://doi.org/10.22038/IJBMS.2017.8668
Article
Google Scholar
Gottschalk M, Xu J, Calzas C, Segura M (2010) Streptococcus suis: a new emerging or an old neglected zoonotic pathogen? Future Microbiol 5(3):371–391. https://doi.org/10.2217/fmb.10.2
Article
PubMed
Google Scholar
Goyettedesjardins G, Auger JP, Xu J, Segura M, Gottschalk M (2014) Streptococcus suis, an important pig pathogen and emerging zoonoticagent—an update on the worldwide distribution based on serotyping and Sequence typing. Emerg Microb Infect 3(6):e45. https://doi.org/10.1038/emi.2014.45
Article
Google Scholar
Grenier D, Grignon L, Gottschalk M (2009) Characterisation of biofilm formation by a Streptococcus suis meningitis isolate. Vet J 179(2):292–295. https://doi.org/10.1016/j.tvjl.2007.09.005
CAS
Article
PubMed
Google Scholar
Guo D, Wang L, Lu C (2012) In vitro biofilm forming potential of Streptococcus suis isolated from human and swine in China. Braz J Microbiol 43(3):993–1004. https://doi.org/10.1590/S1517-838220120003000021
CAS
Article
Google Scholar
Hall CW, Mah TF (2017) Molecular mechanisms of biofilm-based antibiotic resistance and tolerance in pathogenic bacteria. FEMS Microbiol Rev 41(3):276–301. https://doi.org/10.1093/femsre/fux010
Article
PubMed
CAS
Google Scholar
Han X, Lei L, Fan G, Zhang Y, Da X, Zuo J, Wang S, Wang X, Tian M, Chan D (2015) Riemerella anatipestifer Lacks Luxs , but can uptake exogenous autoinducer-2 to regulate biofilm formation. Res Microbiol 166(6):486–493. https://doi.org/10.1016/j.resmic.2015.06.004
CAS
Article
PubMed
Google Scholar
Hao H, Hui W, Liu P, Lv Q, Zeng X, Jiang H, Wang Y, Zheng X, Zheng Y, Li J (2013) Correction: effect of licochalcone a on growth and properties of Streptococcus suis. PLoS One 8(7):e67728. https://doi.org/10.1371/annotation/59a7568c-915d-4d9c-b912-f93af72acdcb
CAS
Article
PubMed
PubMed Central
Google Scholar
Henke JM, Bassler BL (2004) Quorum sensing regulates type III secretion in Vibrio harveyi and Vibrio parahaemolyticus. J Bacteriol 186(12):3794–3805. https://doi.org/10.1128/JB.186.12.3794-3805.2004
CAS
Article
PubMed
PubMed Central
Google Scholar
Huong VTL, Thanh LV, Phu VD, Trinh DT, Inui K, Tung N, Oanh NTK, Trung NV, Hoa NT, Bryant JE (2016) Temporal and spatial association of Streptococcus suis infection in humans and porcine reproductive and respiratory syndrome outbreaks in pigs in northern Vietnam. Epidemiol Infect 144(1):35–44. https://doi.org/10.1017/S0950268815000990
CAS
Article
PubMed
Google Scholar
Jã¸Rgensen MG, Thomason MK, Havelund J, Valentin-Hansen P, Storz G (2013) Dual function of the Mcas small Rna in controlling biofilm formation. Genes Dev 27(10):1132–1145. https://doi.org/10.1101/gad.214734.113
CAS
Article
Google Scholar
Ju CX, Gu HW, Lu CP (2012) Characterization and functional analysis of Atl, a novel gene encoding autolysin in Streptococcus suis. J Bacteriol 194(6):1464–1473. https://doi.org/10.1128/JB.06231-11
CAS
Article
PubMed
PubMed Central
Google Scholar
Kadurugamuwa JL, Beveridge TJ (1999) Membrane vesicles derived from Pseudomonas aeruginosa and Shigella flexneri can be integrated into the surfaces of other gram-negative bacteria. Microbiology 145(Pt 8):2051–2060. https://doi.org/10.1099/13500872-145-8-2051
CAS
Article
PubMed
Google Scholar
Khalifa L, Brosh Y, Gelman D, Coppenhagenglazer S, Beyth S, Poradosucohen R, Que YA, Beyth N, Hazan R (2015) Targeting Enterococcus faecalis biofilms with phage therapy. Appl Environ Microbiol 81(8):2696–2705. https://doi.org/10.1128/AEM.00096-15
CAS
Article
PubMed
PubMed Central
Google Scholar
Kumar JS, Umesha S, Prasad KS, Niranjana P (2016) Detection of quorum sensing molecules and biofilm formation in Ralstonia solanacearum. Curr Microbiol 72(3):297–305. https://doi.org/10.1007/s00284-015-0953-0
CAS
Article
PubMed
Google Scholar
Lay ND, Gottesman S (2012) A complex network of small non-coding Rnas regulate motility in Escherichia coli. Mol Microbiol 86(3):524–538. https://doi.org/10.1111/j.1365-2958.2012.08209.x
CAS
Article
PubMed
Google Scholar
Lewis K (2012) Persister cells: molecular mechanisms related to antibiotic tolerance. Springer, Berlin Heidelberg. https://doi.org/10.1007/978-3-642-28951-4_8
Book
Google Scholar
Li XZ, Nikaido H (2004) Efflux-mediated drug resistance in bacteria: an update. Drugs 64(2):159–204. https://doi.org/10.2165/11317030-000000000-00000
CAS
Article
PubMed
Google Scholar
Li Y, Yang W, Zhe M, Lin HX, Xu B, Grenier D, Fan HJ, Lu CP (2016) Identification and characterization of a Streptococcus equi ssp. zooepidemicus immunogenic Groel protein involved in biofilm formation. Vet Res 47(1):50. https://doi.org/10.1186/s13567-016-0334-0
CAS
Article
Google Scholar
Li YH, Zhou YH, Ren YZ, Xu CG, Liu X, Liu B, Chen JQ, Ding WY, Zhao YL, Yang YB (2018) Inhibition of Streptococcus suis adhesion and biofilm formationin vitroby water extracts Ofrhizoma coptidis. Front Pharmacol 9:371. https://doi.org/10.3389/fphar.2018.00371
Article
PubMed
PubMed Central
Google Scholar
Liu Y, Cui L, Zhao Z, Gang XU, Wang M, Li YH (2009) Antibacterial activity on different extracts of 50 Chinese herbal medicines against Streptococcus suis in vitro. J Northeast Agric Univ 40(07):90–93
Liu Y, Xu G, Wang M, Li HT, Li YH (2010) Narrowing mutant selection window of Streptococcus suis by combination use of tylosin tartrate and amoxicillin sodium in vitro. Chin J Prev Vet Med 32(1):65–67
CAS
Google Scholar
Liu B, Han Q, Sheng ZL, Chen JQ, Chen XY, Wei SG, LI YH(2015) Intervention effects of water extract, Berberine hydrochloride and coptisine from Rhizoma coptidis against Streptococcus suis biofilm in vitro. Zhongguo Shou Yi Za Zhi 51(04):16–19
Lowe BA, Miller JD, Neely MN (2007) Analysis of the polysaccharide capsule of the systemic pathogen Streptococcus iniae and its implications in virulence. Infect Immun 75(3):1255–1264. https://doi.org/10.1128/IAI.01484-06
CAS
Article
PubMed
Google Scholar
Ma F, Yi L, Yu N, Wang G, Ma Z, Lin H, Fan H (2017) Streptococcus suis serotype 2 biofilms inhibit the formation of neutrophil extracellular traps. Front Cell Infect Microbiol 7:86. https://doi.org/10.3389/fcimb.2017.00086
CAS
Article
PubMed
PubMed Central
Google Scholar
Mah TFC, O’Toole GA (2001) Mechanisms of biofilm resistance to antimicrobial agents. Trends Microbiol 9(1):34–39. https://doi.org/10.1016/S0966-842X(00)01913-2
CAS
Article
PubMed
Google Scholar
Mei JJ, Wang Y, Li YI, Zhang JK, Cheng XC, Zhang CJ, Zu-Hua YU, Ting-Cai WU (2016) Effect of oct protein on the biofilm formation and the bacterial adherence of Streptococcus suis. Chin Vet Sci 46(02):192–197
Meng X, Shi Y, Ji W, Meng X, Zhang J, Wang H, Lu C, Sun J, Yan Y (2011) Application of a bacteriophage lysin to disrupt biofilms formed by the animal pathogen Streptococcus suis. Appl Environ Microbiol 77(23):8272–8279. https://doi.org/10.1128/AEM.05151-11
CAS
Article
PubMed
PubMed Central
Google Scholar
Mika F, Hengge R (2013) Small regulatory Rnas in the control of motility and biofilm formation in E. coli and Salmonella. Int J Mol Sci 14(3):4560–4579. https://doi.org/10.3390/ijms14034560
CAS
Article
PubMed
PubMed Central
Google Scholar
Mulcahy H, Charronmazenod L, Lewenza S (2008) Extracellular DNA chelates cations and induces antibiotic resistance in Pseudomonas aeruginosa biofilms. PLoS Pathog 4(11):e1000213. https://doi.org/10.1371/journal.ppat.1000213
CAS
Article
PubMed
PubMed Central
Google Scholar
Neely MN, Pfeifer JD, Caparon M (2002) Streptococcus-zebrafish model of bacterial pathogenesis. Infect Immun 70(7):3904–3914. https://doi.org/10.1128/IAI.70.7.3904-3914.2002
CAS
Article
PubMed
PubMed Central
Google Scholar
Phelps HA, Neely MN (2005) Evolution of the zebrafish model: from development to immunity and infectious disease. Zebrafish 2(2):87–103. https://doi.org/10.1089/zeb.2005.2.87
CAS
Article
PubMed
Google Scholar
Lu P, Jiao A, Chang P, Hu BR, Fu Q, Sun P, Wei J, Li Y (2015) The influence of some biological characteristics on Streptococcus suis irradiated by carbon ion. J Radiat Res Radiat Process 33(01):53–59
Polkade AV, Mantri SS, Patwekar UJ, Jangid K (2016) Quorum sensing: an under-explored phenomenon in the Phylum actinobacteria. Front Microbiol 7:131. https://doi.org/10.3389/fmicb.2016.00131
Article
PubMed
PubMed Central
Google Scholar
Rice KC, Bayles KW (2008) Molecular control of bacterial death and lysis. Microbiol Mol Biol Rev 72(1):85–109. https://doi.org/10.1128/MMBR.00030-07
CAS
Article
PubMed
PubMed Central
Google Scholar
Rohde H, Frankenberger S, Zähringer U, Mack D (2010) Structure, function and contribution of polysaccharide intercellular adhesin (pia) to Staphylococcus epidermidis biofilm formation and pathogenesis of biomaterial-associated infections. Eur J Cell Biol 89(1):103–111. https://doi.org/10.1016/j.ejcb.2009.10.005
CAS
Article
PubMed
Google Scholar
Sauer K, Camper AK, Ehrlich GD, Costerton JW, Davies DG (2002) Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J Bacteriol 184(4):1140–1154. https://doi.org/10.1128/jb.184.4.1140-1154.2002
CAS
Article
PubMed
PubMed Central
Google Scholar
Segura M, Calzas C, Grenier D, Gottschalk M (2016) Initial steps of the pathogenesis of the infection caused by Streptococcus suis: fighting against nonspecific defenses. FEBS Lett 590(21):3772–3799. https://doi.org/10.1002/1873-3468.12364
CAS
Article
PubMed
Google Scholar
Seneviratne CJ, Wang Y, Jin L, Wong SS, Herath TD, Samaranayake LP (2012) Unraveling the resistance of microbial biofilms: has proteomics been helpful? Proteomics 12(4–5):651–665. https://doi.org/10.1002/pmic.201100356
CAS
Article
PubMed
Google Scholar
Shuai W, Yang Y, Zhao Y, Zhao H, Bai J, Chen J, Zhou Y, Chang W, Li Y (2016) Sub-mic tylosin inhibits Streptococcus suis biofilm formation and results in differential protein expression. Frontiers Microbiol 7:384. https://doi.org/10.3389/fmicb.2016.00384
Article
Google Scholar
Southey-Pillig CJ, Davies DG, Sauer K (2005) Characterization of temporal protein production in Pseudomonas aeruginosa biofilms. J Bacteriol 187(23):8114–8126. https://doi.org/10.1128/JB.187.23.8114-8126.2005
CAS
Article
PubMed
PubMed Central
Google Scholar
Stanley NR, Lazazzera BA (2010) Environmental signals and regulatory pathways that influence biofilm formation. Mol Microbiol 52(4):917–924. https://doi.org/10.1111/j.1365-2958.2004.04036.x
CAS
Article
Google Scholar
Stewart PS, Costerton JW (2001) Antibiotic resistance of bacteria in biofilms. Lancet 358(9276):135–138. https://doi.org/10.1016/S0140-6736(01)05321-1
CAS
Article
PubMed
Google Scholar
Sutherland IW (2001) The biofilm matrix – an immobilized but dynamic microbial environment. Trends Microbiol 9(5):222–227. https://doi.org/10.1016/S0966-842X(01)02012-1
CAS
Article
PubMed
Google Scholar
Tanabe S, Bonifait L, Fittipaldi N, Grignon L, Gottschalk M, Grenier D (2010) Pleiotropic effects of polysaccharide capsule loss on selected biological properties of Streptococcus suis. Can J Vet Res 74(1):65–70
CAS
PubMed
PubMed Central
Google Scholar
Thomason MK, Fontaine F, De LN, Storz G (2012) A small Rna that regulates motility and biofilm formation in response to changes in nutrient availability in Escherichia coli. Microbiol Biotechnol 84(1):17–35. https://doi.org/10.1111/j.1365-2958.2012.07965.x
CAS
Article
Google Scholar
Thurnheer T, Gmür R, Shapiro S, Guggenheim B (2003) Mass transport of macromolecules within an in vitro model of supragingival plaque. Appl Environ Microbiol 69(3):1702–1709. https://doi.org/10.1128/AEM.69.3.1702-1709.2003
CAS
Article
PubMed
PubMed Central
Google Scholar
Tian LJ, Zhao Q, Song XY, Liu SM, Ma HX (2014) Antibacterial effect of combination of twenty Chinese herbs with ciprofloxacin against Streptococcus suis in vitro. Chin J Vet Drug 48(01):45–48
Vidal JE, Ludewick HP, Kunkel RM, Zähner D, Klugman KP (2011) The Luxs-dependent quorum-sensing system regulates early biofilm formation by Streptococcus pneumoniae strain D39. Infect Immun 79(10):4050–4060. https://doi.org/10.1128/IAI.05186-11
CAS
Article
PubMed
PubMed Central
Google Scholar
Voegele P, Badiola J, Schmidt-Malan SM, Karau MJ, Greenwood-Quaintance KE, Mandrekar JN, Patel R (2015) Antibiofilm activity of electrical current in a catheter model. Antimicrob Agents Chemother 60(3):1476–1480. https://doi.org/10.1128/AAC.01628-15
CAS
Article
PubMed
Google Scholar
Vogeleer P, Tremblay YD, Mafu AA, Jacques M, Harel J (2014) Life on the outside: role of biofilms in environmental persistence of Shiga-toxin producing Escherichia coli. Front Microbiol 5(317):317. https://doi.org/10.3389/fmicb.2014.00317
Article
PubMed
PubMed Central
Google Scholar
Wang Y, Zhang W, Wu Z, Lu C (2011a) Reduced virulence is an important characteristic of biofilm infection of Streptococcus suis. FEMS Microbiol Lett 316(1):36–43. https://doi.org/10.1111/j.1574-6968.2010.02189.x
CAS
Article
PubMed
Google Scholar
Wang Y, Zhang W, Wu Z, Zhu X, Lu C (2011b) Functional analysis of Luxs in Streptococcus suis reveals a key role in biofilm formation and virulence. Vet Microbiol 152(1):151–160. https://doi.org/10.1016/j.vetmic.2011.04.029
CAS
Article
PubMed
Google Scholar
Wang Y, Yi L, Wu Z, Shao J, Liu G, Fan H, Zhang W, Lu C (2012) Comparative proteomic analysis of Streptococcus suis biofilms and planktonic cells that identified biofilm infection-related immunogenic proteins. PLoS One 7(4):e33371. https://doi.org/10.1371/journal.pone.0033371
CAS
Article
PubMed
PubMed Central
Google Scholar
Wang Y, Yi L, Zhang Z, Fan H, Cheng X, Lu C (2013) Overexpression of Luxs cannot increase autoinducer-2 production, only affect the growth and biofilm formation in Streptococcus suis. Sci World J 2013(2):924276. https://doi.org/10.1155/2013/924276
CAS
Article
Google Scholar
Wang Y, Yi L, Zhang Z, Fan H, Cheng X, Lu C (2014) Biofilm formation, host-cell adherence, and virulence genes regulation of Streptococcus suis in response to autoinducer-2 signaling. Curr Microbiol 68(5):575–580. https://doi.org/10.1007/s00284-013-0509-0
CAS
Article
PubMed
Google Scholar
Wang Y, Li Y, Wang S, Fan H, Ding C, Mao X, Lu C (2015a) Crystal structure and identification of two key amino acids involved in Ai-2 production and biofilm formation in Streptococcus suis Luxs. PLoS One 10(10):e0138826. https://doi.org/10.1371/journal.pone.0138826
CAS
Article
PubMed
PubMed Central
Google Scholar
Wang Y, Yi L,Shi MY,Zhang C, Liu YC, Zhang L, Li XK, Yu ZH, Zhang CJ, Cheng XC (2015b) Method for constructing animal model of bacterial biofilm infection in vivo. China Patent No. ZL201,110,427,983.3. China Patent Office
Wang S, Wang C, Gao L, Cai H, Zhou Y, Yang Y, Xu C, Ding W, Chen J, Muhammad I (2017) Rutin inhibits Streptococcus suis biofilm formation by affecting Cps biosynthesis. Front Pharmacol 8:379. https://doi.org/10.3389/fphar.2017.00379
Article
PubMed
PubMed Central
Google Scholar
Wang Y, Wang Y, Sun L, Grenier D, Yi L (2018) The Luxs/Ai-2 system of Streptococcus suis. Appl Microbiol Biotechnol 102:7231–7238. https://doi.org/10.1007/s00253-018-9170-7
CAS
Article
Google Scholar
Williamson KS, Richards LA, Perezosorio AC, Pitts B, Mcinnerney K, Stewart PS, Franklin MJ (2012) Heterogeneity in Pseudomonas aeruginosa biofilms includes expression of ribosome hibernation factors in the antibiotic-tolerant subpopulation and hypoxia-induced stress response in the metabolically active population. J Bacteriol 194(8):2062–2073. https://doi.org/10.1128/JB.00022-12
CAS
Article
PubMed
PubMed Central
Google Scholar
Wu Z, Zhang W, Lu C (2008) Comparative proteome analysis of secreted proteins of Streptococcus suis serotype 9 isolates from diseased and healthy pigs. Microb Pathog 45(3):159–166. https://doi.org/10.1016/j.micpath.2008.04.009
CAS
Article
PubMed
Google Scholar
Wu Z, Zhang W, Lu Y, Lu C (2010) Transcriptome profiling of zebrafish infected with Streptococcus suis. Microb Pathog 48(5):178–187. https://doi.org/10.1016/j.micpath.2010.02.007
CAS
Article
PubMed
Google Scholar
Xiao G, Tang H, Zhang S, Ren H, Dai J, Lai L, Lu C, Yao H, Fan H, Wu Z (2017) Streptococcus suis small Rna Rss04 contributes to the induction of meningitis by regulating capsule synthesis and by inducing biofilm formation in a mouse infection model. Vet Microbiol 199:111–119. https://doi.org/10.1016/j.vetmic.2016.12.034
CAS
Article
PubMed
Google Scholar
Xue T, Ni J, Shang F, Chen X, Zhang M (2015) Autoinducer-2 increases biofilm formation via an Ica- and Bhp-dependent manner in Staphylococcus epidermidis Rp62a. Microb Infect 17(5):345–352. https://doi.org/10.1016/j.micinf.2015.01.003
CAS
Article
Google Scholar
Yang YB, Chen JQ, Zhao YL, Bai JW, Ding WY, Zhou YH, Chen XY, Liu D, Li YH (2016) Sub-mics of azithromycin decrease biofilm formation of Streptococcus suis and increase capsular polysaccharide content of S. suis. Front Microbiol 7(e89059). https://doi.org/10.3389/fmicb.2016.01659
Yi L, Wang Y, Ma Z, Zhang H, Li Y, Zheng JX, Yang YC, Fan HJ, Lu CP (2014) Biofilm formation of Streptococcus equi Ssp . zooepidemicus and comparative proteomic analysis of biofilm and planktonic cells. Curr Microbiol 69(3):227–233. https://doi.org/10.1007/s00284-014-0574-z
CAS
Article
PubMed
Google Scholar
Zhang H, Ma Z, Li Y, Zheng J, Li Y, Fan H, Lu C (2013) Identification of a novel collagen type I-binding protein from Streptococcus suis serotype 2. Vet J 197(2):406–414. https://doi.org/10.1016/j.tvjl.2013.01.030
CAS
Article
PubMed
Google Scholar
Zhao YL, Zhou YH, Chen JQ, Huang QY, Han Q, Liu B, Cheng GD, Li YH (2015) Quantitative proteomic analysis of sub-mic erythromycin inhibiting biofilm formation of S. suis in vitro. J Proteom 116:1–14. https://doi.org/10.1016/j.jprot.2014.12.019
CAS
Article
Google Scholar