Volume 32, Number 7—July 2026
Dispatch
Nipah Virus Shedding in Urine from Fruit Bats, Sri Lanka, 2018–2019
Table 1
Primers and cycling conditions for quantitative PCR assay developed for study of NiV shedding in urine from fruit bats, Sri Lanka, 2018–2019
| Component |
Conditions |
| Primers | |
| NiV_F | AAA TCA AGT TGC AGA ACT CGC T |
| NiV_R | CTC CRA TGA GCA CAC CTC CTG |
| NiV Probe |
FAM-CTT CCT GCT GAT GTT TC- MGB |
| Protocol† |
AgPath-ID One-Step RT-PCR Kit,‡ 6 µL H20, 12.5 µL RT buffer, 1 µL NiV_F (10 µM), 1 µL NiV_R (10 µM), 0.5 µL NiVN_probe (10 µM), 1.0 µL enzyme mix (25×) |
| Cycling conditions |
45°C for 900 s, 95°C for 600 s, 95°C for 15 s for 45 cycles, 60°C for 45 s |
| Cycler types | Light Cycler 480,§ ABI 7500,‡ Bio-Rad CFX 96¶ |
*F, forward primer; FAM, fluorescein amidites; MGB, minor groove binder; NiV, Nipah virus; R, reverse primer. †The primers listed are all included in the mix. ‡Applied Biosystems, https://www.thermofisher.com. §Roche Life Science, https://lifescience.roche.com. ¶Bio-Rad Laboratories, https://www.bio-rad.com.
1These first authors contributed equally to this article.
Page created: April 13, 2026
Page updated: June 26, 2026
Page reviewed: June 26, 2026
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.