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Measles Vaccine Virus RNA in Children More Than 100 Days after Vaccination
Jamie McMahon1,2, Ian M Mackay3,4, Stephen B Lambert4
1Public Health Virology Laboratory, Forensic and Scientific Services, 39 Kessels Road, Coopers Plains, QLD 4108, Australia. jamie.mcmahon@uqconnect.edu.au.
Abstract:
Measles vaccines have been in use since the 1960s with excellent safety and effectiveness profiles. Limited data are available on detection of measles vaccine virus (MeVV) RNA in human subjects following vaccination. Available evidence suggests MeVV RNA can be identified up to 14 days after vaccination, with detection beyond this rare. In routine diagnostic testing, we used two real-time reverse transcription-polymerase chain reaction (RT-rPCR) assays targeting M and F genes to identify measles virus (MeV) and MeVV RNA. Confirmatory testing was performed with an N gene RT-rPCR, followed by sequence confirmation of RT-rPCR positives by semi-nested conventional RT-PCR assays targeting portions of the N, H, and L genes. We report detection and confirmation of MeVV RNA from the respiratory tract of 11 children between 100 and 800 days after most recent receipt of measles-containing vaccine. These novel findings emphasize the importance of genotyping all MeV detections and highlight the need for further work to assess whether persistent MeVV RNA represents viable virus and if transmission to close contacts can occur.
Insights
Measles vaccine virus (MeVV) RNA was detected in children long after vaccination. Further research is needed to determine if this persistent RNA indicates viable virus or potential transmission.
Area of Science:
- Virology
- Immunology
- Public Health
Background:
- Measles vaccines, in use since the 1960s, possess strong safety and efficacy.
- Limited data exist regarding the detection of measles vaccine virus (MeVV) RNA in individuals post-vaccination.
- Current understanding suggests MeVV RNA detection is typically confined to 14 days post-vaccination, with longer detection being uncommon.
Purpose of the Study:
- To investigate the prolonged detection of measles vaccine virus (MeVV) RNA in children.
- To analyze the implications of detecting MeVV RNA beyond the established short timeframe.
- To emphasize the necessity of viral genotyping for all measles virus detections.
Main Methods:
- Utilized real-time reverse transcription-polymerase chain reaction (RT-rPCR) assays targeting M and F genes for MeV and MeVV RNA identification.
- Employed N gene RT-rPCR for confirmatory testing.
- Performed sequence confirmation using semi-nested conventional RT-PCR assays targeting N, H, and L genes.
Main Results:
- Successfully detected and confirmed MeVV RNA in the respiratory tracts of 11 children.
- Detection occurred between 100 and 800 days post-most recent measles-containing vaccine administration.
- This finding represents a significant extension of previously documented MeVV RNA detection timelines.
Conclusions:
- The prolonged presence of MeVV RNA in the respiratory tract challenges existing knowledge.
- Highlights the critical importance of genotyping all measles virus detections to distinguish between wild-type and vaccine strains.
- Underscores the need for further investigation into whether persistent MeVV RNA signifies viable virus and its potential for transmission.
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