SEAFDEC/AQDINSTITUTIONAL REPOSITORY
    • English
    • 日本語
    • ไทย
    • Bahasa Indonesia
  • English 
    • English
    • 日本語
    • ไทย
    • Bahasa Indonesia
  • Login
View Item 
  •   SEAFDEC/AQD Institutional Repository Home
  • 03 SEAFDEC/AQD External Publications
  • Journal Articles, Conference Papers and Book Chapters by SEAFDEC Staff
  • Journal Articles
  • View Item
  •   SEAFDEC/AQD Institutional Repository Home
  • 03 SEAFDEC/AQD External Publications
  • Journal Articles, Conference Papers and Book Chapters by SEAFDEC Staff
  • Journal Articles
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Molecular typing of Vibrio parahaemolyticus strains isolated from the Philippines by PCR-based methods

  • Global styles
  • MLA
  • Vancouver
  • Elsevier - Harvard
  • APA
  • Help
Thumbnail
View/Open
Date
2005
Author
Maluping, R. P.
Ravelo, C.
Lavilla-Pitogo, C. R.
Krovacek, K.
Romalde, J. L.
Page views
1,989
ASFA keyword
nucleotide sequence ASFA
microbiological strains ASFA
DNA ASFA
polymerase chain reaction ASFA
genomes ASFA
genetic isolation ASFA
microbiology ASFA
AGROVOC keyword
Typing
random amplified polymorphic DNA AGROVOC
Conserved sequence
Vibrio parahaemolyticus AGROVOC
Penaeus monodon AGROVOC
Philippines AGROVOC
Giant tiger prawn
Enterobacterial repetitive intergenic consensus sequence PCR,
Repetitive extragenic palindromic PCR
Taxonomic term
Penaeus monodon GBIF
Metadata
Show full item record


Share 
 
Abstract
Aim: The main aim of the present study was to use three PCR-based techniques for the analysis of genetic variability among Vibrio parahaemolyticus strains isolated from the Philippines.

Methods and Results: Seventeen strains of V. parahaemolyticus isolated from shrimps (Penaeus monodon) and from the environments where these shrimps are being cultivated were analysed by random amplified polymorphic DNA PCR (RAPD-PCR), enterobacterial repetitive intergenic consensus sequence PCR (ERIC-PCR) and repetitive extragenic palindromic PCR (REP-PCR). The results of this work have demonstrated genetic variability within the V. parahaemolyticus strains that were isolated from the Philippines. In addition, RAPD, ERIC and REP-PCR are suitable rapid typing methods for V. parahaemolyticus. All three methods have good discriminative ability and can be used as a rapid means of comparing V. parahaemolyticus strains for epidemiological investigation. Based on the results of this study, we could say that REP-PCR is inferior to RAPD and ERIC-PCR owing to the fact that it is less reproducible. Moreover, the REP-PCR analysis yielded a relatively small number of products. This may suggests that the REP sequences may not be widely distributed in the V. parahaemolyticus genome.

Conclusions: Genetic variability within V. parahaemolyticus strains isolated in the Philippines has been demonstrated. The presence of ERIC and REP sequences in the genome of this bacterial species was confirmed. Significance and Impact of the Study:The RAPD, ERIC and REP-PCR techniques are useful methods for molecular typing of V. parahaemolyticus strains. To our knowledge this is the first study of this kind carried out on V. parahaemolyticus strains isolated from the Philippines.
URI
http://hdl.handle.net/10862/1668
Suggested Citation
Maluping, R. P., Ravelo, C., Lavilla-Pitogo, C. R., Krovacek, K., & Romalde, J. L. (2005). Molecular typing of Vibrio parahaemolyticus strains isolated from the Philippines by PCR-based methods. Journal of Applied Microbiology, 99(2), 383-391. https://doi.org/10.1111/j.1365-2672.2005.02571.x 
DOI
10.1111/j.1365-2672.2005.02571.x
Type
Article
ISSN
1364-5072
Collections
  • Journal Articles [1267]

Related items

Showing items related by title, author, creator and subject.

  • Thumbnail

    Genome analysis of Pasteurella piscicida 

    Naka, Hiroaki; Hirono, Ikuo; Aoki, Takashi (Fish Health Section, Asian Fisheries Society, 2002)
    Genome analysis was conducted to detect the virulence genes in Pasteurella piscicida (Photobacterium damsela subsp. piscicida) KP9038. To date, we have analyzed 366 clones and determined 333,341 bp nucleotide sequences. As a result of comparison of these clones to the GenBank database, these clones were separated into functional categories; small-molecule metabolism, broad regulatory functions, macro-molecule metabolism, cell processes and others. At present, five clones from the genome analysis have been deduced to have homology with reported virulence genes. These are DsbA (required for enterotoxin biogenesis), nucleotide sugar epimerase, OpsX (lipopolysaccharide biosynthesis), LspA2 (filamentous hemagglutinin) and PldA (outer membrane phospholipase A).
  • Thumbnail

    Milkfish (Chanos chanos) growth hormone cDNA cloning and mRNA expression in embryos and early larval stages. 

    de Jesus, Evelyn Grace T.; Ayson, Felix G.; Amemiya, Yutaka; Moriyama, Shunsuke; Hyodo, Susumu; Hirano, Tetsuya; Kawauchi, Hiroshi (Elsevier, 2002)
    In an attempt to understand growth regulation in milkfish, the milkfish growth hormone (GH) and its cDNA were characterized and the expression of GH mRNA in embryos and larvae was examined by RT-PCR. The milkfish GH was purified from an alkaline extract of the pituitary by reverse-phase high-performance liquid chromatography and detected as an immuno-positive protein with anti-salmon GH serum. The complete sequence of milkfish pre-GH was determined by cDNA cloning and nucleotide sequencing. On the basis of the N-terminal amino acid analysis of the native protein, the pre-GH was found to consist of a signal peptide of 22 amino acids and a mature protein of 188 amino acids. Milkfish GH shows higher amino acid sequence identity with GHs of carps (91–94%) and salmonids (70%) than with GHs of more advanced teleosts (<60%) in good accordance with its taxonomic position in teleosts. It has five half Cys residues, four of which are at positions homologous with those of other known GHs and the extra Cys with those of carp GHs. The molecular weight of milkfish GH was estimated to be 22 kDa, which is comparable to the theoretical value. This suggests that milkfish GH is a simple protein, although it has two potential N-glycosylation sites. Semiquantitative RT-PCR showed that GH mRNA expression was relatively weak in embryos and newly hatched larvae but was already strong in 2-day old and older larvae.
  • Thumbnail

    Morphological and genetic diversity assessment of freshwater prawns (Macrobrachium spp.) in the Cairawan river, Antique province, Panay island, Philippines 

    Santos, Mary Nia M.; Wowor, Daisy ORCID; Ikeda, Minoru; Padilla, Philip Ian ORCID; Romana-Eguia, Maria Rowena R. ORCID (National Fisheries Research and Development Institute, 2024)
    Freshwater prawns of the genus Macrobrachium are among the most valuable cultured aquatic species in the world. The systematic study of Macrobrachium species in the Philippines has often been based on morphological trait assessment. Here, we combined morphology and molecular approaches to study the presence and actual distribution of Macrobrachium species along the Cairawan River in Laua-an, Antique Province, Panay Island. Using morphological characteristics, we identified 11 Macrobrachium species, the highest number of species reported from a single river. Molecular results based on the cytochrome oxidase subunit I (COI) mitochondrial DNA (mtDNA) sequences confirmed the morphological identification. The analysis revealed eight major clades with 19 distinct haplotypes within the species. Our results provide information on the identification of Macrobrachium species inhabiting the Cairawan River. The baseline information can be helpful for future genetic studies involving freshwater prawns with potential use in aquaculture. It can provide scientific data to facilitate the formulation of selective breeding plans and direct governance policies in freshwater prawn resource conservation and management in the Philippines.

© SEAFDEC/AQD  2026
Send Feedback | Subscribe
 

 

Browse

All of SAIRCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

My Account

LoginRegister

Statistics

View Usage Statistics

© SEAFDEC/AQD  2026
Send Feedback | Subscribe
 

 

Export citations

Export the current results of the search query as a citation list. Select one of the available citation styles, or add a new one using the "Citations format" option present in the "My account" section.

The list of citations that can be exported is limited to items.

Export citations

Export the current item as a citation. Select one of the available citation styles, or add a new one using the "Citations format" option present in the "My account" section.

Export Citations

DOCUMENT REQUEST NOT AVAILABLE

This publication is still available (in PRINT) and for sale at AQD bookstore. The library is currently restricted to send PDF of publications that are still for sale.

You may contact bookstore@seafdec.org.ph or visit AQD bookstore for orders.

FILE UNDER EMBARGO

This file associated with this publication is currently under embargo. This will be available for download after the embargo date.