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Molecular typing of Mannheimia (Pasteurella) haemolytica serotype A1 isolates from cattle in Japan
K Katsuda1, M Kohmoto, K Kawashima
1Environmental Hygiene Section, Shichinohe Research Unit, National Institute of Animal Health, 31 Uminai, Shichinohe, Kamikita, Aomori 039-2586, Japan.
Abstract:
Pulsed field gel electrophoresis (PFGE) and random amplified polymorphic DNA (RAPD) methods were applied for molecular typing of 130 Mannheimia (Pasteurella) haemolytica serotype A1 isolates obtained from 13 prefectures in Japan. These isolates were divided into 15 ApaI PFGE profiles that formed six distinct clusters (clusters A-F). Fifty-three (40.7%) isolates were classified in cluster B, and 20.0, 13.8, 12.3, 6.9 and 6.1% of isolates were in clusters E, A, F, D and C, respectively. The isolates of cluster B were differentiated into seven subtypes (B1-B7) and subtype B5 contained 63% (34/53) of isolates. RAPD revealed four banding patterns (types I-IV), and among 130 isolates 60.7% (79/130) of isolates were RAPD type I. All of the RAPD type I isolates were grouped into clusters A-C by PFGE. There was no relationship between molecular typing and geographic origin of these isolates. These results indicate that isolates of M. haemolytica A1 strain with various molecular profiles have already spread in Japan and may have caused sporadic infections.
Insights
Molecular typing of Mannheimia (Pasteurella) haemolytica serotype A1 in Japan revealed diverse genetic profiles. These diverse strains have spread across the country, potentially causing sporadic infections.
Area of Science:
- Veterinary Microbiology
- Molecular Epidemiology
- Bacterial Pathogenesis
Background:
- Mannheimia (Pasteurella) haemolytica serotype A1 is an important bovine respiratory disease pathogen.
- Understanding the genetic diversity and distribution of M. haemolytica A1 is crucial for disease control.
Purpose of the Study:
- To perform molecular typing of M. haemolytica A1 isolates from Japan using Pulsed Field Gel Electrophoresis (PFGE) and Random Amplified Polymorphic DNA (RAPD).
- To investigate the genetic diversity and population structure of M. haemolytica A1 in Japan.
Main Methods:
- DNA extraction from 130 M. haemolytica A1 isolates collected from 13 Japanese prefectures.
- Molecular typing using ApaI PFGE and RAPD analysis.
- Cluster analysis of PFGE profiles.
Main Results:
- Fifteen ApaI PFGE profiles were identified, forming six distinct clusters (A-F), with cluster B being the most prevalent (40.7%).
- Subtyping of cluster B revealed seven subtypes, with B5 being the most common (63%).
- RAPD analysis yielded four banding patterns, with type I comprising 60.7% of isolates; RAPD type I isolates were associated with PFGE clusters A-C.
Conclusions:
- M. haemolytica A1 isolates in Japan exhibit significant molecular diversity.
- No correlation was found between molecular type and geographic origin, suggesting widespread dissemination.
- The diverse and widespread nature of these strains may contribute to sporadic disease outbreaks.
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