Project Details
Abstract
Angiostrongyliasis is an important zoonosis in Taiwan. In the permissive hosts (rats), the
fifth-stage larvae (L5) of Angiostrongylus cantonensis in the brain penetrate the blood brain
barrier, migrate to the right ventricle and pulmonary arteries, and develop into adults. However,
L5 remain in the subaranoid cavity and cause eosinophilic meningitis and eosinophilic
meningoencephalitis in non-permissive hosts such as humans and mice.
In our previous studies, there are significant differences between L5 from SD rats and ICR mice in
survival duration, average length, and injuries to the hosts. The present study is going to
understand the differences in development, survival, and pathogenic mechanisms at the
transcriptomics and proteomics levels. The expressions of genes and proteins of these two L5 were
compared with the next generation sequencing (NGS) and two-dimensional protein electrophoresis
(2-DE) coupled with mass spectrometry (MS) technologies. The results will be helpful on developing
effective diagnostic techniques and therapeutic strategies of angiostrongyliasis.
This study is a three-year project. The first year project is being implemented. The study has
constructed a NGS data set from the fifth stage larvae of A. cantonensis collected from SD rats.
Analyzing this data set, 13,483,766 raw reads can be assembled to 31,487 unique clusters. In
addition, a data set of L5 from ICR mice has been nearing completion. When finished, we would
analyze these two data sets to investigate the genes expression differences in the survival of
these two L5.
In the follow-up studies:
In the first year, differences in the protein expressions between L5 from the two kinds of hosts
were compared with analytical technologies of proteomics. 2-DE is employed to identify protein
expression profiles to select proteins with significantly different expressions. The peptide mass
fingerprinting of these proteins are then determined by MALDI-TOF.
In the second year, the amino acid sequences of two types of L5 are matched with the NGS database
to confirm the protein sequence and identity. The functional annotation of these proteins should be
helpful in the investigation of the survival of L5 between permissive hosts and non-permissive
hosts. Moreover, matching of gene and protein expressions is also useful for the understanding of
the mechanisms in the regulation of gene and protein expressions.
Project IDs
Project ID:PC10112-0042
External Project ID:NSC101-2320-B182-045
External Project ID:NSC101-2320-B182-045
Status | Finished |
---|---|
Effective start/end date | 01/08/12 → 31/07/13 |
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