Literature DB >> 11513665

Identification of species in animal feedstuffs by polymerase chain reaction--restriction fragment length polymorphism analysis of mitochondrial DNA.

F Bellagamba1, V M Moretti, S Comincini, F Valfrè.   

Abstract

Restriction site analysis of Polymerase Chain Reaction (PCR) products of cytochrome b mitochondrial DNA was applied to identify species in meat meal and animal feedstuffs. PCR was used to amplify a variable region of cytochrome b mitochondrial DNA gene. Species differentiation was determined by digestion of the obtained 359 bp amplicon with restriction enzymes, which generated species-specific electrophoresis patterns; the sequencing of PCR products was used as confirming analysis. PCR-RFLP analysis revealed the presence of meat meal in animal feedstuffs and distinguished species of interest. The results supported the application of the method in control measures which should be adopted for meat-meal-based animal feed, as suggested by EU law. As a technical improvement, to simplify the analysis, the number of enzymes presented in this study for the detection of different species was smaller than others described in the literature; discrimination between ruminant and nonruminant species and between mammalian and poultry species was possible with few digestions.

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Year:  2001        PMID: 11513665     DOI: 10.1021/jf0010329

Source DB:  PubMed          Journal:  J Agric Food Chem        ISSN: 0021-8561            Impact factor:   5.279


  13 in total

1.  The 'BSE Strategic Project' of the National Council of Research: results of four years of research.

Authors:  F Valfrè; V M Moretti
Journal:  Vet Res Commun       Date:  2003-09       Impact factor: 2.459

2.  Detection of cross-contamination in feedstuffs: presence of constituents of animal origin.

Authors:  L Pinotti; F Bellagamba; R Paratte; G Savoini; V Dell'Orto
Journal:  Vet Res Commun       Date:  2003-09       Impact factor: 2.459

Review 3.  Traceability issues in fishery and aquaculture products.

Authors:  V M Moretti; G M Turchini; F Bellagamba; F Caprino
Journal:  Vet Res Commun       Date:  2003-09       Impact factor: 2.459

4.  A preliminary trial using multi-target polymerase chain reaction (multiplex PCR) and restriction fragment length polymorphism (PCR-RFLP) on the same feedstuffs to detect tissues of animal origin.

Authors:  F Colombo; E Marchisio; I E Trezzi; V Peri; L Pinotti; A Baldi; G Soncini
Journal:  Vet Res Commun       Date:  2004-08       Impact factor: 2.459

5.  An alternative method to isoenzyme profile for cell line identification and interspecies cross-contaminations: cytochrome b PCR-RLFP analysis.

Authors:  Claretta G Losi; Stefania Ferrari; Enrico Sossi; Riccardo Villa; Maura Ferrari
Journal:  In Vitro Cell Dev Biol Anim       Date:  2008-07-02       Impact factor: 2.416

6.  Establishment of a molecular tool for blood meal identification in Malaysia.

Authors:  Ernieenor Faraliana Che Lah; Mariana Ahamad; Mohd Subail Haron; Ho Tze Ming
Journal:  Asian Pac J Trop Biomed       Date:  2012-03

7.  PCR-RFLP analysis: a promising technique for host species identification of blood meals from tsetse flies (Diptera: Glossinidae).

Authors:  Stephan Steuber; Ahmed Abdel-Rady; Peter-Henning Clausen
Journal:  Parasitol Res       Date:  2005-07-06       Impact factor: 2.289

8.  Species identification of cattle and buffalo fat through PCR assay.

Authors:  S Vaithiyanathan; V V Kulkarni
Journal:  J Food Sci Technol       Date:  2016-04-19       Impact factor: 2.701

9.  Development of species identification tests targeting the 16S ribosomal RNA coding region in mitochondrial DNA.

Authors:  Kazuhiko Imaizumi; Tomoko Akutsu; Sachio Miyasaka; Mineo Yoshino
Journal:  Int J Legal Med       Date:  2006-11-16       Impact factor: 2.686

10.  Using species-specific repeat and PCR-RFLP in typing of DNA derived from blood of human and animal species.

Authors:  Yasser Said El-Sayed; Omnia Ismaeil Mohamed; Khaled Mohamed Ashry; Salah M Abd El-Rahman
Journal:  Forensic Sci Med Pathol       Date:  2009-11-28       Impact factor: 2.007

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