Establishment of a Direct PCR Assay for Simultaneous Differential Diagnosis of African Swine Fever and Classical Swine Fever Using Crude Tissue Samples.
African swine fever
classical swine fever
crude nucleic acid extraction
multiplex detection
real-time reverse-transcription polymerase chain reaction
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
28 02 2022
28 02 2022
Historique:
received:
26
01
2022
revised:
17
02
2022
accepted:
25
02
2022
entrez:
26
3
2022
pubmed:
27
3
2022
medline:
15
4
2022
Statut:
epublish
Résumé
African swine fever (ASF) and classical swine fever (CSF) are contagious swine diseases that are clinically indistinguishable from each other; hence, reliable test methods for accurate diagnosis and differentiation are highly demanded. By employing a buffer system suitable for crude extraction of nucleic acids together with an impurity-tolerant enzyme, we established a multiplex assay of real-time reverse-transcription polymerase chain reaction (rRT-PCR) for simultaneous detection of ASF virus (ASFV), CSF virus (CSFV) and swine internal control derived genes in a sample without the need for prior purification of viral nucleic acids. We applied this method to test serum and tissue samples of infected pigs and wild boars and compared the statistical sensitivities and specificities with those of standard molecular diagnostic methods. When a serum was used as a test material, the newly established assay showed 94.4% sensitivity for both and 97.9 and 91.9% specificity for ASFV and CSFV detection, respectively. In contrast, the results were 100% identical with those obtained by the standard methods when a crude tissue homogenate was used as a test material. The present data indicate that this new assay offers a practical, quick, and reliable technique for differential diagnosis of ASF and CSF where geographical occurrences are increasingly overlapping.
Identifiants
pubmed: 35336904
pii: v14030498
doi: 10.3390/v14030498
pmc: PMC8948687
pii:
doi:
Substances chimiques
Nucleic Acids
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Références
Vet Res. 2020 Jul 31;51(1):96
pubmed: 32736657
J Vet Med Sci. 2021 Jan 5;82(12):1835-1845
pubmed: 33162428
Rev Sci Tech. 1990 Mar;9(1):151-61
pubmed: 1966720
J Virol Methods. 2005 Dec;130(1-2):36-44
pubmed: 16055202
Virol J. 2011 May 02;8:201
pubmed: 21535885
Emerg Infect Dis. 2019 Jun;25(6):1228-1231
pubmed: 30870139
Viruses. 2017 Apr 21;9(4):
pubmed: 28430168
Arch Virol. 1994;136(3-4):309-23
pubmed: 8031236
Adv Virus Res. 2015;93:47-160
pubmed: 26111586
Transbound Emerg Dis. 2021 Apr 23;:
pubmed: 33890426
Natl Inst Anim Health Q (Tokyo). 1981 Winter;21(4):153-8
pubmed: 7200574
J Gen Virol. 2018 May;99(5):613-614
pubmed: 29565243
J Vet Med Sci. 2019 Sep 3;81(9):1277-1284
pubmed: 31292349
Transbound Emerg Dis. 2013 Feb;60(1):48-58
pubmed: 22394449
J Virol Methods. 2003 Jan;107(1):53-61
pubmed: 12445938
Emerg Microbes Infect. 2021 Dec;10(1):2183-2193
pubmed: 34709128
Viruses. 2019 Mar 30;11(4):
pubmed: 30935026
Transbound Emerg Dis. 2018 Dec;65(6):1482-1484
pubmed: 30102848
J Comp Pathol. 2015 Jan;152(1):9-21
pubmed: 25443146
Sci Rep. 2021 Feb 26;11(1):4759
pubmed: 33637799
J Immunol Methods. 2005 Nov 30;306(1-2):16-27
pubmed: 16223507
Virus Res. 2013 Apr;173(1):122-30
pubmed: 23137735