2019
DOI: 10.1016/j.micinf.2018.12.001
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Pertactin-deficient Bordetella pertussis isolates in Poland—a country with whole-cell pertussis primary vaccination

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Cited by 19 publications
(13 citation statements)
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“…All 170 isolates contained sequences encoding the same protein as the tcfA2 allele, which is reactive with the pertussis LFIA. Broadening our geographic focus, we reviewed 784 other B. pertussis isolates for which TcfA sequence information was available 34,[36][37][38][39][40] . Only 19 of these isolates were from the U.S. 34,39 .…”
Section: Resultsmentioning
confidence: 99%
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“…All 170 isolates contained sequences encoding the same protein as the tcfA2 allele, which is reactive with the pertussis LFIA. Broadening our geographic focus, we reviewed 784 other B. pertussis isolates for which TcfA sequence information was available 34,[36][37][38][39][40] . Only 19 of these isolates were from the U.S. 34,39 .…”
Section: Resultsmentioning
confidence: 99%
“…Only 19 of these isolates were from the U.S. 34,39 . The remaining 765 were from Poland, the Netherlands, China, the United Kingdom, Finland, Sweden, France, Germany, Japan, Italy, and Belgium (listed in descending order based on the number of isolates sourced from each country) 34,[36][37][38][39][40] . These isolates were collected between 1949 and 2017 34,[36][37][38][39][40] .…”
Section: Resultsmentioning
confidence: 99%
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“…Bordetella holmesii strain ATCC 51541 (DSM 13416) was obtained from DSMZ collection (Leibniz-Institut, Berlin, Germany). B. pertussis strains 186 and 606, used in the current wP vaccine manufactured in Poland, were acquired from the National Medicines Institute (Warsaw, Poland) [ 30 ]. Bordetella parapertussis PCM 529 (ATCC 15311), Bordetella bronchiseptica PCM 530 (ATCC 19395), and Bordetella bronchiseptica PCM 1943 (ATCC 4617) came from the PCM collection (Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland).…”
Section: Methodsmentioning
confidence: 99%
“…Przeprowadzone badania molekularne wykazały, że brak syntezy pertaktyny nie był wynikiem ekspansji pojedynczego klonu lecz był skutkiem powstania niezależnych mutacji. Opisano szereg mechanizmów takich jak: insercja IS481 lub IS1002 w gen kodujący Prn, delecja całego genu prn lub jego fragmentów, pojawienie się kodonu STOP w miejscu powodującym przedwczesne zakończenie syntezy białka, insercja guaniny do homopolimerycznego fragmentu poly(G) prowadząca do odwracalnego przesunięcia ramki odczytu w mechanizmie zmienności fazowej, inwersja części promotora prn, tranzycja G → A w pozycji -162 uniemożliwiająca transkrypcję genu prn, a także dotychczas niezidentyfikowane mutacje występujące poza promotorem oraz rejonem kodującym genu prn [76].…”
Section: Bordetella Pertussisunclassified