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Rapid detection of viral antibodies based on multifunctional Staphylococcus aureus nanobioprobes

Identifieur interne : 001049 ( Main/Exploration ); précédent : 001048; suivant : 001050

Rapid detection of viral antibodies based on multifunctional Staphylococcus aureus nanobioprobes

Auteurs : Jinjuan Qiao [République populaire de Chine] ; Yunpeng Li [République populaire de Chine] ; Cuihua Wei [République populaire de Chine] ; Hang Yang [République populaire de Chine] ; Junping Yu [République populaire de Chine] ; Hongping Wei [République populaire de Chine]

Source :

RBID : PMC:7112379

Descripteurs français

English descriptors

Abstract

Biosynthesis of nanoparticles inside S. aureus cells has enhanced the sensitivity of immunoassays based on the S. aureus nanoparticles. However, the current methods are limited to antigen detection by conjugating IgG antibodies on S. aureus nanoparticles. In this study, a simple way to conjugate antigens to the S. aureus nanobioparticles was developed by utilizing a cell wall binding domain (CBD) from a bacteriophage lysin PlyV12. Based on this novel design, simple agglutination tests of the IgG antibodies of Ebola virus (EBOV) nucleoprotein (NP) and Middle East Respiratory Virus (MERS) NP in rabbit sera were successfully developed by conjugating the S. aureus nanobioparticles with two fusion proteins EBOV NP- CBD and MERS NP-CBD, respectively. The conjugation was done easily by just mixing the fusion proteins with the S. aureus nanoparticles. The detection time was within 20 min without any special equipment or expertise. As far as we know, this is the first time to realize the detection of viral antibodies based on S. aureus nanoparticles.


Url:
DOI: 10.1016/j.enzmictec.2016.09.006
PubMed: 27866631
PubMed Central: 7112379


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Biosynthesis of nanoparticles inside
<italic>S. aureus</italic>
cells has enhanced the sensitivity of immunoassays based on the
<italic>S. aureus</italic>
nanoparticles. However, the current methods are limited to antigen detection by conjugating IgG antibodies on
<italic>S. aureus</italic>
nanoparticles. In this study, a simple way to conjugate antigens to the
<italic>S. aureus</italic>
nanobioparticles was developed by utilizing a cell wall binding domain (CBD) from a bacteriophage lysin PlyV12. Based on this novel design, simple agglutination tests of the IgG antibodies of Ebola virus (EBOV) nucleoprotein (NP) and Middle East Respiratory Virus (MERS) NP in rabbit sera were successfully developed by conjugating the
<italic>S. aureus</italic>
nanobioparticles with two fusion proteins EBOV NP- CBD and MERS NP-CBD, respectively. The conjugation was done easily by just mixing the fusion proteins with the
<italic>S. aureus</italic>
nanoparticles. The detection time was within 20 min without any special equipment or expertise. As far as we know, this is the first time to realize the detection of viral antibodies based on
<italic>S. aureus</italic>
nanoparticles.</p>
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</tree>
</affiliations>
</record>

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