Synthesis of conjugated PIA-rSesC and immunological evaluation against biofilm-forming Staphylococcus epidermidis

被引:14
|
作者
Mirzaei, Bahman [1 ,2 ]
Mousavi, Seyed Fazlollah [1 ]
Babaei, Reyhane [2 ]
Bahonar, Sara [2 ]
Siadat, Seyed Davar [3 ]
Ardestani, Mehdi Shafiee [4 ]
Shahrooei, Mohammad [5 ]
Van Eldere, John [5 ]
机构
[1] Pasteur Inst Iran, Microbial Res Ctr, Dept Microbiol, Tehran, Iran
[2] Mazandaran Univ Med Sci, Dept Med Microbiol & Virol, Fac Med, Sari, Iran
[3] Pasteur Inst Iran, Microbiol Res Ctr, Mycobacteriol & Pulm Res Dept, Tehran, Iran
[4] Univ Tehran Med Sci, Dept Radiopharm, Fac Pharm, Tehran, Iran
[5] Katholieke Univ Leuven, Dept Med Diagnost Sci, Lab Med Microbiol, UZ Gasthuisberg, Herestr 49,CDG 8th Floor, B-3000 Leuven, Belgium
关键词
PIA-based conjugate vaccine; biofilm-forming Staphylococcus epidermidis; polysaccharide intracellular adhesin; ICA LOCUS; IDENTIFICATION; ACCUMULATION; PURIFICATION; INFECTIONS; INHIBITION; ANTIBODIES; MECHANISM; PROTEINS; VACCINES;
D O I
10.1099/jmm.0.000910
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Purpose. Staphylococcus epidermidis is an opportunistic pathogen and a leading cause of morbidity and premature mortality in patients with medical device-related infections, which is a concern in hospitalized patients. Developing a strategy to raise opsonic antibodies against polysaccharide intracellular adhesin (PIA) could be promising for the elimination of colonizing and biofilm-forming S. epidermidis. Following the purification of truncated rSesC protein and PIA, for the first time, PIA was conjugated to rSesC as a carrier to increase the immunogenicity of PIA and its efficacy in mice was evaluated. The structure of the conjugate was analysed using the Fourier transform infrared spectroscopy (FTIR) and proton nuclear magnetic resonance spectroscopy (H1-NMR) methods. Afterwards, the immune response was evaluated by measuring the total IgG, IgG2a and IgG2b titres. Results. The immunization of mice with the PIA-rSesC conjugate raised the levels of opsonic antibodies, and the vaccinated mice were protected when challenged intravenously by wild-type S. epidermidis strain 1457. Further studies indicated that the conjugated vaccine was able to eliminate S. epidermidis biofilm formation in in vitro or in vivo assays. Conclusion. This study confirms the proposal that the immunization of mice with PIA-rSesC conjugate vaccine could protect against S. epidermidis infection.
引用
收藏
页码:791 / 802
页数:12
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