Development and characterization of secondary standards for nucleic acid amplification technology (NAAT) assays for detection of hepatitis E virus
Published by Elsevier B.V..
BACKGROUND: To harmonize assays for detection of HEV RNA, a World Health Organization International Standard (WHO IS) was established. The WHO IS represents the highest order standard for HEV RNA but is limited in quantity. Secondary standards are needed to limit the use of WHO IS and minimize the need to replace it.
OBJECTIVE: Establish secondary standards for HEV NAAT assays and to calibrate these against the WHO IS.
METHODS: Stocks of genotype 3 HEV were prepared using both cell lysates and cell culture supernatants to produce non-enveloped and quasi-enveloped virus stocks, respectively. Both stocks were heat-inactivated, diluted in negative human plasma, and lyophilized to produce two candidate secondary standards: HEV-RR (non-enveloped virus) and HEV-RR.1 (quasi-enveloped virus). Both candidate standards were characterized and calibrated against the WHO IS for HEV RNA in an international collaborative study.
RESULTS: The collaborative study returned a total of 15 data sets, with different RNA extraction and amplification methods. The estimated mean values relative to the WHO IS (250,000 IU/ml) are 229,000 IU/ml and 355,000 IU/ml for HEV-RR and HEV-RR.1, respectively.
CONCLUSION: We have established two secondary standards for HEV RNA calibrated against the WHO IS. These standards are non-infectious and stable under different storage temperatures.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
Zur Gesamtaufnahme - volume:157 |
---|---|
Enthalten in: |
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology - 157(2022) vom: 17. Dez., Seite 105325 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Fares-Gusmao, Rafaelle [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 25.11.2022 Date Revised 02.12.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.jcv.2022.105325 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM349088403 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM349088403 | ||
003 | DE-627 | ||
005 | 20231226041807.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jcv.2022.105325 |2 doi | |
028 | 5 | 2 | |a pubmed24n1163.xml |
035 | |a (DE-627)NLM349088403 | ||
035 | |a (NLM)36395548 | ||
035 | |a (PII)S1386-6532(22)00257-8 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Fares-Gusmao, Rafaelle |e verfasserin |4 aut | |
245 | 1 | 0 | |a Development and characterization of secondary standards for nucleic acid amplification technology (NAAT) assays for detection of hepatitis E virus |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 25.11.2022 | ||
500 | |a Date Revised 02.12.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Published by Elsevier B.V. | ||
520 | |a BACKGROUND: To harmonize assays for detection of HEV RNA, a World Health Organization International Standard (WHO IS) was established. The WHO IS represents the highest order standard for HEV RNA but is limited in quantity. Secondary standards are needed to limit the use of WHO IS and minimize the need to replace it | ||
520 | |a OBJECTIVE: Establish secondary standards for HEV NAAT assays and to calibrate these against the WHO IS | ||
520 | |a METHODS: Stocks of genotype 3 HEV were prepared using both cell lysates and cell culture supernatants to produce non-enveloped and quasi-enveloped virus stocks, respectively. Both stocks were heat-inactivated, diluted in negative human plasma, and lyophilized to produce two candidate secondary standards: HEV-RR (non-enveloped virus) and HEV-RR.1 (quasi-enveloped virus). Both candidate standards were characterized and calibrated against the WHO IS for HEV RNA in an international collaborative study | ||
520 | |a RESULTS: The collaborative study returned a total of 15 data sets, with different RNA extraction and amplification methods. The estimated mean values relative to the WHO IS (250,000 IU/ml) are 229,000 IU/ml and 355,000 IU/ml for HEV-RR and HEV-RR.1, respectively | ||
520 | |a CONCLUSION: We have established two secondary standards for HEV RNA calibrated against the WHO IS. These standards are non-infectious and stable under different storage temperatures | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, U.S. Gov't, P.H.S. | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Biological standards | |
650 | 4 | |a Hepatitis E virus | |
650 | 4 | |a Molecular testing | |
650 | 4 | |a Nucleic acid tests | |
650 | 4 | |a Secondary standards | |
650 | 4 | |a Standardization | |
650 | 7 | |a RNA, Viral |2 NLM | |
700 | 1 | |a Jiang, Zhen |e verfasserin |4 aut | |
700 | 1 | |a Subramaniam, Sakthivel |e verfasserin |4 aut | |
700 | 1 | |a Visser, Bryan J |e verfasserin |4 aut | |
700 | 1 | |a Scott, Alysia |e verfasserin |4 aut | |
700 | 1 | |a Ishida, Yuji |e verfasserin |4 aut | |
700 | 1 | |a Saito, Takeshi |e verfasserin |4 aut | |
700 | 1 | |a Baylis, Sally A |e verfasserin |4 aut | |
700 | 1 | |a McGivern, David R |e verfasserin |4 aut | |
700 | 0 | |a HEV Standard Calibration Study Group |e verfasserin |4 aut | |
700 | 1 | |a Osiowy, Carla |e investigator |4 oth | |
700 | 1 | |a Borlang, Jamie |e investigator |4 oth | |
700 | 1 | |a Kosowan, Tyler |e investigator |4 oth | |
700 | 1 | |a Baylis, Sally A |e investigator |4 oth | |
700 | 1 | |a Kleiber, Roswitha |e investigator |4 oth | |
700 | 1 | |a Wenzel, Jürgen J |e investigator |4 oth | |
700 | 1 | |a Schemmerer, Mathias |e investigator |4 oth | |
700 | 1 | |a Klein, Jasmin |e investigator |4 oth | |
700 | 1 | |a Pisani, Giulio |e investigator |4 oth | |
700 | 1 | |a Simeoni, Matteo |e investigator |4 oth | |
700 | 1 | |a Martina, Antonio |e investigator |4 oth | |
700 | 1 | |a Sakata, Hidekatsu |e investigator |4 oth | |
700 | 1 | |a Iida, Juri |e investigator |4 oth | |
700 | 1 | |a Kobayashi, Yu |e investigator |4 oth | |
700 | 1 | |a Hogema, Boris |e investigator |4 oth | |
700 | 1 | |a Molenaar-de Backer, Marijke |e investigator |4 oth | |
700 | 1 | |a Niesters, Hubert G |e investigator |4 oth | |
700 | 1 | |a Rurenga-Gard, Lilli |e investigator |4 oth | |
700 | 1 | |a Hayden, Tonya |e investigator |4 oth | |
700 | 1 | |a Kamili, Saleem |e investigator |4 oth | |
700 | 1 | |a Cox, Heather |e investigator |4 oth | |
700 | 1 | |a Dyer, Nicole |e investigator |4 oth | |
700 | 1 | |a Wu, Priscilla |e investigator |4 oth | |
700 | 1 | |a Linnen, Jeff |e investigator |4 oth | |
700 | 1 | |a Cooper, Jasmine |e investigator |4 oth | |
700 | 1 | |a Livezey, Kristin |e investigator |4 oth | |
773 | 0 | 8 | |i Enthalten in |t Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology |d 1997 |g 157(2022) vom: 17. Dez., Seite 105325 |w (DE-627)NLM097223964 |x 1873-5967 |7 nnns |
773 | 1 | 8 | |g volume:157 |g year:2022 |g day:17 |g month:12 |g pages:105325 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.jcv.2022.105325 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 157 |j 2022 |b 17 |c 12 |h 105325 |