A PCR protocol to establish standards for routine mycoplasma testing that by design detects over ninety percent of all known mycoplasma species

被引:9
作者
Siegl, Dominik [1 ]
Kruchem, Marie [1 ]
Jansky, Sandrine [1 ]
Eichler, Emma [1 ]
Thies, Dorothe [1 ]
Hartwig, Udo [2 ,5 ]
Schuppan, Detlef [1 ,3 ,4 ,5 ]
Bockamp, Ernesto [1 ,3 ,5 ]
机构
[1] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Translat Immunol TIM, D-55131 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Med Hematol & Med Oncol 3, D-55131 Mainz, Germany
[3] Immune NTech GmbH, D-55234 Wendelsheim, Germany
[4] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Div Gastroenterol, Boston, MA 02215 USA
[5] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Res Ctr Immunotherapy, D-55131 Mainz, Germany
关键词
SP NOV; CELL-CULTURES; GEN; NOV; CONTAMINATION; INFECTION; SPECIFICITY; SENSITIVITY; PRECURSORS; COMPONENTS; EXPRESSION;
D O I
10.1016/j.isci.2023.106724
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mycoplasma infection leads to false and non-reproducible scientific data and poses a risk to human health. Despite strict guidelines calling for regular myco-plasma screening, there is no universal and widely established standard proced-ure. Here, we describe a reliable and cost-effective PCR method that establishes a universal protocol for mycoplasma testing. The applied strategy utilizes ultra -conserved eukaryotic and mycoplasma sequence primers covering by design 92% of all species in the six orders of the class Mollicutes within the phylum My-coplasmatota and is applicable to mammalian and many non-mammalian cell types. This method can stratify mycoplasma screening and is suitable as a com-mon standard for routine mycoplasma testing.
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页数:14
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