Mutation of ompA gene of Shigellajlexneri: towards development of an oral live attenuated Shigella vaccine
Shigellosis is one of the major infectious diseases in the world. Each year in developing country, Shigella spp. cause illness in over 150 million individuals and death in over one million (Kotloff et al., 1999). Children under the age of 5 are most severely affected. In developing countries, S....
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| Format: | Monograph |
| Language: | English |
| Published: |
Pusat Pengajian Sains Perubatan Universiti Sains Malaysia
2008
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| Subjects: | |
| Online Access: | http://eprints.usm.my/50456/1/LIM%20MENG%20HUANG%20-%2024%20pages.pdf http://eprints.usm.my/50456/ |
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| Summary: | Shigellosis is one of the major infectious diseases in the world. Each year in
developing country, Shigella spp. cause illness in over 150 million individuals and death in
over one million (Kotloff et al., 1999). Children under the age of 5 are most severely
affected. In developing countries, S. flexneri and S. sonnei are the most prevalent species,
causing about 60% and 15% of episodes, respectively.
The enormous global burden of Shigella, augmented by the growing rate of antimicrobial
resistance, makes development of an effective vaccine essential. At present there
is no vaccine against Shigella, although a variety of live and subunit vaccines which elicit
an anti-LPS mucosal response have been shown to confer protection in experimental
models of shigellosis (Levine et al., 1976; Sanchez et al., 1994; Jennison et al., 2004).
Live, attenuated Shigella strains have been the dominant approach to Shigella
vaccine development since a 1966 report (Formal et al., 1 966) showing that monkeys were
protected against subsequent disease if previously administered attenuated organisms.
S . .flexneri poses a structural gene, ompA which encodes tbr outer membrane protein
A. Outer membrane protein A adds to the stability of the cell envelope by linking the outer
membrane to the peptidoglycan. Therefore, in this study the gene of interest is ompA
whereby the gene will be mutated by insertional mutation. The mutants are assumed to
induce protective immunity against shigellosis. In this study, ompA has been mutated by
using kanamycin resistance gene (aphA). The use of this antibiotic resistance gene is to
facilitate the process of manipulating the genes as it serves as a selective marker. The
creation of the construct ompA::aphA is to facilitate the approach into the development of a
potential live attenuated Shigella vaccine. |
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