Abstract:
:Analysis of actA gene sequence polymorphism has been shown to be an effective and relatively inexpensive method for subtyping Listeria monocytogenes isolates, allowing the division of the population of this species into two deeply separate lineages. This sequence-based method as well as PCR-mediated fingerprinting were applied here for the differentiation of 49 isolates of food and clinical origin. Correlation between these two typing approaches was high. Both methods divided the isolates into two lineages, designated I (33 isolates) and II (16 isolates). All the 33 lineage I isolates were assigned to the same, or closely related, six clusters by both typing methods. For the lineage II isolates, PCR fingerprinting was found to be more discriminatory. The isolates were characterized by cell invasion assay. All highly invasive isolates were assigned to lineage I, which constituted a heterogeneous group also containing low-invasive isolates. High-invasive isolates were not found in the genetically determined lineage II. A particular actA cluster, designated Ha, contained all the isolates showing the lowest invasiveness. A common trait of the isolates belonging to this cluster was the presence of a threonine-441 of the deduced ActA sequence instead of the alanine-441 present in the remaining isolates. Thirteen human isolates were classified to lineage I and five to lineage II. A PCR-based method can therefore differentiate L. monocytogenes isolates in accordance with the current phylogenetic model of the evolution of this species.
journal_name
Folia Microbiol (Praha)journal_title
Folia microbiologicaauthors
Bania J,Zarczyńska A,Molenda J,Dabrowska A,Kosek-Paszkowska K,Wieckowska-Szakiel M,Rózalska Bdoi
10.1007/s12223-009-0003-zsubject
Has Abstractpub_date
2009-01-01 00:00:00pages
17-24issue
1eissn
0015-5632issn
1874-9356journal_volume
54pub_type
杂志文章abstract::Single chain Fv (scFv) antibodies (generated by phage display technology, molecules representing new and efficient tools in the research and diagnostics of infectious diseases) against the capsid protein (p25) of Maedi-Visna virus were selected. Several clones of p25 specific scFv antibodies were identified; one of th...
journal_title:Folia microbiologica
pub_type: 杂志文章
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
pub_type: 杂志文章
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
pub_type: 杂志文章
doi:10.1007/BF02906811
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journal_title:Folia microbiologica
pub_type: 杂志文章
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更新日期:2001-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
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更新日期:2003-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
doi:10.1007/BF02931370
更新日期:2003-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
doi:10.1007/s12223-017-0568-x
更新日期:2018-05-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
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更新日期:1983-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章,评审
doi:10.1007/s12223-018-0626-z
更新日期:2018-09-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
doi:10.1007/BF02935823
更新日期:1991-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章
doi:10.1007/BF02814514
更新日期:1991-01-01 00:00:00
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journal_title:Folia microbiologica
pub_type: 杂志文章,评审
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
pub_type: 杂志文章
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更新日期:2000-01-01 00:00:00
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journal_title:Folia microbiologica
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journal_title:Folia microbiologica
pub_type: 杂志文章
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journal_title:Folia microbiologica
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更新日期:2007-01-01 00:00:00
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journal_title:Folia microbiologica
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更新日期:1982-01-01 00:00:00
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journal_title:Folia microbiologica
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更新日期:1997-01-01 00:00:00
abstract::Procedures to introduce point mutations, restriction sites and insert or delete DNA fragments are very important tools to study protein function. We describe here two-step PCR-based method for generating single or multiple mutations, insertions and deletions in a small region of the sequence. In the first step, a uniq...
journal_title:Folia microbiologica
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