tetano
Editor, Senior Moderator
Front Vet Sci
. 2024 Mar 7:11:1304022.
doi: 10.3389/fvets.2024.1304022. eCollection 2024. Inactivation of highly transmissible livestock and avian viruses including influenza A and Newcastle disease virus for molecular diagnostics
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.
. 2024 Mar 7:11:1304022.
doi: 10.3389/fvets.2024.1304022. eCollection 2024. Inactivation of highly transmissible livestock and avian viruses including influenza A and Newcastle disease virus for molecular diagnostics
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
- PMID: 38515532
- PMCID: PMC10955088
- DOI: 10.3389/fvets.2024.1304022
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
- PMID: 38515532
- PMCID: PMC10955088
- DOI: 10.3389/fvets.2024.1304022
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.
Jennifer L Welch[SUP] 1 [/SUP], Ram Shrestha[SUP] 1 [/SUP], Heather Hutchings[SUP] 1 [/SUP], Narinder Pal[SUP] 1 [/SUP], Randall Levings[SUP] 1 [/SUP], Suelee Robbe-Austerman[SUP] 1 [/SUP], Rachel Palinski[SUP] 1 [/SUP], Karthik K Shanmuganatham[SUP] 1 [/SUP]
Affiliations
- PMID: 38515532
- PMCID: PMC10955088
- DOI: 10.3389/fvets.2024.1304022
There is a critical need for an inactivation method that completely inactivates pathogens at the time of sample collection while maintaining the nucleic acid quality required for diagnostic PCR testing. This inactivation method is required to alleviate concerns about transmission potential, minimize shipping complications and cost, and enable testing in lower containment laboratories, thereby enhancing disease diagnostics through improved turn-around time. This study evaluated a panel of 10 surrogate viruses that represent highly pathogenic animal diseases. These results showed that a commercial PrimeStore® molecular transport media (PSMTM) completely inactivated all viruses tested by >99.99%, as determined by infectivity and serial passage assays. However, the detection of viral nucleic acid by qRT-PCR was comparable in PSMTM and control-treated conditions. These results were consistent when viruses were evaluated in the presence of biological material such as sera and cloacal swabs to mimic diagnostic sample conditions for non-avian and avian viruses, respectively. The results of this study may be utilized by diagnostic testing laboratories for highly pathogenic agents affecting animal and human populations. These results may be used to revise guidance for select agent diagnostic testing and the shipment of infectious substances.
Keywords: animal virus; inactivation; influenza virus; molecular diagnostics; molecular transport media.