TY - JOUR
T1 - Simultaneous and rapid detection method for measles and rubella using single-tube multiplex real-time quantitative RT-PCR
AU - Yoshioka, Nori
AU - Hagiya, Hideharu
AU - Deguchi, Matsuo
AU - Hamaguchi, Shigeto
AU - Kagita, Masanori
AU - Tomono, Kazunori
N1 - Funding Information:
RNA standards of measles and rubella were provided by Dr. Yoshio Mori and Dr. Fumio Seki, National Institute of Infectious Diseases, Japan.
Publisher Copyright:
© 2019 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases
PY - 2019/10
Y1 - 2019/10
N2 - Patients with measles or rubella infections manifest acute onset fever accompanying systemic exanthema, which are clinically difficult to be distinguish. Rapid diagnosis and differentiation of such epidemic viral diseases is essential to prevent outbreaks. We developed a single-tube multiplex real-time PCR assay for these indistinguishable viruses. We used previously-reported primer settings, with a slight modification of reporter dye, and applied to multiplex Taqman real-time PCR by cobas z480 (Roche Molecular Systems, Inc.). Consequently, the assay could detect 10 copies/10 μl of measles and rubella with coefficient of variations of 11.2% and 21.8%, respectively. Strengths of our methodology include simplicity of operation, short measurement time (2 h), uses of internal control (confirming a run of PCR), and quantitative measurement with high sensitivity. Both measles and rubella currently cause social outbreaks in Japan. We hope that our single-tube multiplex assay contributes to an early diagnosis, leading to an appropriate infection control measure and prevention of epidemics.
AB - Patients with measles or rubella infections manifest acute onset fever accompanying systemic exanthema, which are clinically difficult to be distinguish. Rapid diagnosis and differentiation of such epidemic viral diseases is essential to prevent outbreaks. We developed a single-tube multiplex real-time PCR assay for these indistinguishable viruses. We used previously-reported primer settings, with a slight modification of reporter dye, and applied to multiplex Taqman real-time PCR by cobas z480 (Roche Molecular Systems, Inc.). Consequently, the assay could detect 10 copies/10 μl of measles and rubella with coefficient of variations of 11.2% and 21.8%, respectively. Strengths of our methodology include simplicity of operation, short measurement time (2 h), uses of internal control (confirming a run of PCR), and quantitative measurement with high sensitivity. Both measles and rubella currently cause social outbreaks in Japan. We hope that our single-tube multiplex assay contributes to an early diagnosis, leading to an appropriate infection control measure and prevention of epidemics.
KW - Infection control
KW - Measles
KW - Rapid diagnosis
KW - Rubella
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U2 - 10.1016/j.jiac.2019.05.005
DO - 10.1016/j.jiac.2019.05.005
M3 - Article
C2 - 31253475
AN - SCOPUS:85067943367
SN - 1341-321X
VL - 25
SP - 829
EP - 831
JO - Journal of Infection and Chemotherapy
JF - Journal of Infection and Chemotherapy
IS - 10
ER -