Multilocus Sequence Typing of Non-JP2 Serotype b Aggregatibacter actinomycetemcomitans Strains of Ghanaian and Swedish Origin

被引:1
|
作者
Claesson, Rolf [1 ]
Johansson, Anders [2 ]
Hoeglund Aberg, Carola [2 ]
Esberg, Anders [3 ]
Haubek, Dorte [4 ]
Oscarsson, Jan [1 ]
机构
[1] Umea Univ, Dept Odontol, Div Oral Microbiol, Umea, Sweden
[2] Umea Univ, Dept Odontol, Div Mol Periodontol, Umea, Sweden
[3] Umea Univ, Dept Odontol, Umea, Sweden
[4] Aarhus Univ, Dept Dent & Oral Hlth, Sect Paediat Dent, Aarhus, Denmark
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2021年 / 11卷
关键词
Aggregatibacter actinomycetemcomitans; multilocus sequence typing (MLST); non-JP2; serotype b; cagE; evolutionary analysis; genomic analysis; ARBITRARILY PRIMED PCR; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS; JP2; CLONE; AGGRESSIVE PERIODONTITIS; LOCALIZED JUVENILE; LEUKOTOXIN; EXPRESSION; REPRODUCIBILITY; MICROBIOLOGY; ADOLESCENT;
D O I
10.3389/fcimb.2021.769671
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective and MethodsThe Gram-negative bacterium, Aggregatibacter actinomycetemcomitans is associated with periodontitis affecting young individuals. The geographic dissemination of the highly leukotoxic JP2 genotype of serotype b of this species was previously studied by multilocus sequence typing (MLST). Here, we have used MLST to genetically characterize non-JP2 genotype strains of serotype b, isolated from individuals living in Ghana (n=41), and in Sweden (n=13), respectively. ResultsThe MLST analysis revealed a total of nine sequence types (ST). Both Ghanaian and Swedish isolates were distributed in ST 1-3. ST 5 and 6 were only identified among the Ghanaian strains, whereas ST 4, 7, 8 and 9 were uniquely represented among the Swedish strains. Previously, we characterized these non-JP2 genotype strains of A. actinomycetemcomitans serotype b by arbitrarily-primed (AP)-PCR, which distributed them into three groups, AP-PCR type 1, 2, and 3, respectively. AP-PCR type 1 strains are generally highly leukotoxic, and are associated with progression of periodontal attachment loss. As AP-PCR type 1 includes both JP2 genotype strains and a proportion of non-JP2 genotype strains of serotype b, a straightforward diagnostic procedure has been sought. This has revealed a gene, cagE, which appears to be conserved only in this AP-PCR type. According to our results, MLST was not a highly discriminatory method to identify AP-PCR type 1, as strains of this AP-PCR type could be found within three different ST: ST 2, ST 3 and ST 8. ConclusionAccording to MLST, a geographic dissemination of non-JP2 genotype A. actinomycetemcomitans serotype b appears to exist. However, aiming to identify carriers of AP-PCR type 1, non-JP2 genotype serotype b, PCR with cagE-specific primers is likely the most efficient diagnostic procedure known today.
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页数:8
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