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26.11.2021 | Brief Report

Evidence of coinfection of pigs with African swine fever virus and porcine circovirus 2

verfasst von: William G. Dundon, Giovanni Franzo, Tirumala B. K. Settypalli, N.L.P. Indi Dharmayanti, Ulaankhuu Ankhanbaatar, Indrawati Sendow, Atik Ratnawati, Tserenchimed Sainnokhoi, Umberto Molini, Giovanni Cattoli, Charles E. Lamien

Erschienen in: Archives of Virology | Ausgabe 1/2022

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Abstract

Archival swine DNA samples from Indonesia and Mongolia, some of which were previously shown to be positive for African swine fever virus, were screened for the presence of porcine circovirus 2 (PCV-2) and porcine circovirus 3 (PCV-3) by PCR. Samples from both countries were positive for PCV-2 (three from Mongolia and two from Indonesia), while none were positive for PCV-3. The PCV-2 amplicons were sequenced, and phylogenetic analysis revealed that the PCV-2 strains belonged to four different genotypes: PCV-2a (Mongolia), PCV-2b (Mongolia and Indonesia), PCV-2d (Indonesia), and PCV-2g (Mongolia). This is the first report of ASFV/PCV-2 coinfection in pigs and the first report of the presence of PCV-2 in Mongolia.

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Díaz C, Celer V, Frébort I (2020) The main DNA viruses significantly affecting pig livestock. J Vet Res 65:15–25CrossRef

Breitbart M, Delwart E, Rosario K, Segalés J, Varsani A (2017) ICTV report consortium. ICTV virus taxonomy profile: circoviridae. J Gen Virol 98:1997–1998CrossRef

Segalés J (2012) Porcine circovirus type 2 (PCV2) infections: clinical signs, pathology and laboratory diagnosis. Virus Res 164:10–19CrossRef

Palinski R, Piñeyro P, Shang P, Yuan F, Guo R, Fang Y, Byers E, Hause BM (2016) A novel porcine circovirus distantly related to known circoviruses is associated with porcine dermatitis and nephropathy syndrome and reproductive failure. J Virol 91:e01879-e1916PubMedPubMedCentral

Klaumann F, Correa-Fiz F, Franzo G, Sibila M, Núñez JI, Segalés J (2018) Current knowledge on Porcine circovirus 3 (PCV-3): A novel virus with a yet unknown impact on the swine industry. Front Vet Sci 5:1–13CrossRef

Rakibuzzaman A, Ramamoorthy S (2021) Comparative immunopathogenesis and biology of recently discovered porcine circoviruses. Transbound Emerg Dis. https://doi.org/10.1111/tbed.14244CrossRefPubMed

Franzo G, Segalés J (2018) Porcine circovirus 2 (PCV-2) genotype update and proposal of a new genotyping methodology. PLoS ONE 13:e0208585CrossRef

Wang Y, Noll L, Lu N, Porter E, Stoy C, Zheng W, Liu X, Peddireddi L, Niederwerder M, Bai J (2020) Genetic diversity and prevalence of porcine circovirus type 3 (PCV3) and type 2 (PCV2) in the Midwest of the USA during 2016–2018. Transbound Emerg Dis 67:1284–1294CrossRef

Dixon LK, Sun H, Roberts H (2019) African swine fever. Antivir Res 165:34–41CrossRef

10.

Blome S, Franzke K, Beer M (2020) African swine fever—a review of current knowledge. Virus Res 287:198099CrossRef

11.

Normile D (2019) African swine fever marches across much of Asia. Science 364:617–618CrossRef

12.

Opriessnig T, Halbur PG (2012) Concurrent infections are important for expression of porcine circovirus associated disease. Virus Res 164:20–32CrossRef

13.

Kim J, Chung HK, Jung T, Cho WS, Choi C, Chae C (2002) Postweaning multisystemic wasting syndrome of pigs in Korea: prevalence, microscopic lesions and coexisting microorganisms. J Vet Med Sci 64:57–62CrossRef

14.

Dorr PM, Baker RB, Almond GW, Wayne SR, Gebreyes WA (2007) Epidemiologic assessment of porcine circovirus type 2 coinfection with other pathogens in swine. J Am Vet Med Assoc 230:244–250CrossRef

15.

Chen N, Huang Y, Ye M, Li S, Xiao Y, Cui B, Zhu J (2019) Co-infection status of classical swine fever virus (CSFV), porcine reproductive and respiratory syndrome virus (PRRSV) and porcine circoviruses (PCV2 and PCV3) in eight regions of China from 2016 to 2018. Infect Genet Evol 68:127–135CrossRef

16.

Dinh PX, Nguyen MN, Nguyen HT, Tran VH, Tran QD, Dang KH, Vo DT, Le HT, Nguyen NTT, Nguyen TT, Do DT (2021) Porcine circovirus genotypes and their copathogens in pigs with respiratory disease in southern provinces of Vietnam. Arch Virol 166:403–411CrossRef

17.

Dharmayanti NI, Sendow I, Ratnawati A, Settypalli TBK, Saepulloh M, Dundon WG, Nuradji H, Naletoski I, Cattoli G, Lamien CE (2021) African swine fever in North Sumatra and West Java provinces in 2019 and 2020, Indonesia. Transbound Emerg Dis 68:2890–2896CrossRef

18.

Ankhanbaatar U, Sainnokhoi T, Khanui B, Ulziibat G, Jargalsaikhan T, Purevtseren D, Settypalli TBK, Flannery J, Dundon WG, Basan G, Batten C, Cattoli G, Lamien CE (2021) African swine fever virus genotype II in Mongolia, 2019. Transbound Emerg Dis 68:2787–2794CrossRef

19.

Duvigneau JC, Hartl RT, Groiss S, Gemeiner M (2005) Quantitative simultaneous multiplex real-time PCR for the detection of porcine cytokines. J Immunol Methods 306:16–27CrossRef

20.

Ku X, Chen F, Li P, Wang Y, Yu X, Fan S, Qian P, Wu M, He Q (2017) Identification and genetic characterization of porcine circovirus type 3 in China. Transbound Emerg Dis 64:703–708CrossRef

21.

Abascal F, Zardoya R, Telford MJ (2010) TranslatorX: multiple alignment of nucleotide sequences guided by amino acid translations. Nucleic Acid Res 38:W7-13CrossRef

22.

Ragonnet-Cronin M, Hodcroft E, Hué S, Fearnhill E, Delpech V, Brown AJ, Lycett S (2013) UK HIV Drug Resistance Database. Automated analysis of phylogenetic clusters. BMC Bioinform 14:317CrossRef

23.

King DP, Reid SM, Hutchings GH, Grierson SS, Wilkinson PJ, Dixon LK, Bastos AD, Drew TW (2003) Development of a TaqMan PCR assay with internal amplification control for the detection of African swine fever virus. J Virol Methods 107:53–61CrossRef

24.

Franzo G, Cortey M, Segalés J, Hughes J, Drigo M (2016) Phylodynamic analysis of porcine circovirus type 2 reveals global waves of emerging genotypes and the circulation of recombinant forms. Mol Phylogenet Evolut 100:269–280CrossRef

25.

Manokaran G, Lin YN, Soh ML, Lim EA, Lim CW, Tan BH (2008) Detection of porcine circovirus type 2 in pigs imported from Indonesia. Vet Microbiol 132:165–170CrossRef

26.

Jajanathan S, Toung OP, Yee PL, Yew TD, Yoon CP, Keong LB (2011) Genetic characterization of porcine circovirus 2 found in Malaysia. Virol J 8:437CrossRef

27.

Jantafong T, Boonsoongnern A, Poolperm P, Urairong K, Lekcharoensuk C, Lekcharoensuk P (2011) Genetic characterization of porcine circovirus type 2 in piglets from PMWS-affected and -negative farms in Thailand. Virol J 8:88CrossRef

28.

Huynh TM, Nguyen BH, Nguyen VG, Dang HA, Mai TN, Tran TH, Ngo MH, Le VT, Vu TN, Ta TK, Vo VH, Kim HK, Park BK (2014) Phylogenetic and phylogeographic analyses of porcine circovirus type 2 among pig farms in Vietnam. Transbound Emerg Dis 61:e25-34CrossRef

29.

Chae C (2012) Porcine circovirus type 2 and its associated diseases in Korea. Virus Res 164:107–113CrossRef

30.

Cai L, Ni J, Xia Y, Zi Z, Ning K, Qiu P, Li X, Wang B, Liu Q, Hu D, Yu X, Zhou Z, Zhai X, Han X, Tian K (2012) Identification of an emerging recombinant cluster in porcine circovirus type 2. Virus Res 165:95–102CrossRef

31.

Zhai SL, Chen SN, Xu ZH, Tang MH, Wang FG, Li XJ, Sun BB, Deng SF, Hu J, Lv DH, Wen XH, Yuan J, Luo ML, Wei WK (2014) Porcine circovirus type 2 in China: an update on and insights to its prevalence and control. Virol J 11:88CrossRef

32.

Bao F, Mi S, Luo Q, Guo H, Tu C, Zhu G, Gong W (2018) Retrospective study of porcine circovirus type 2 infection reveals a novel genotype PCV2f. Transbound Emerg Dis 65:432–440CrossRef

33.

Han L, Yuan GF, Chen SJ, Dai F, Hou LS, Fan JH, Zuo YZ (2021) Porcine circovirus type 2 (PCV2) infection in Hebei Province from 2016 to 2019: a retrospective study. Arch Virol 166:2159–2171CrossRef

34.

Kwon T, Yoo SJ, Park CK, Lyoo YS (2017) Prevalence of novel porcine circovirus 3 in Korean pig populations. Vet Microbiol 207:178–180CrossRef

35.

Kedkovid R, Woonwong Y, Arunorat J, Sirisereewan C, Sangpratum N, Lumyai M, Kesdangsakonwut S, Teankum K, Jittimanee S, Thanawongnuwech R (2018) Porcine circovirus type 3 (PCV3) infection in grower pigs from a Thai farm suffering from porcine respiratory disease complex (PRDC). Vet Microbiol 215:71–76CrossRef

36.

Sukmak M, Thanantong N, Poolperm P, Boonsoongnern A, Ratanavanichrojn N, Jirawattanapong P, Woonwong Y, Soda N, Kaminsonsakul T, Phuttapatimok S, Wajjwalku W (2019) The retrospective identification and molecular epidemiology of porcine circovirus type 3 (PCV3) in swine in Thailand from 2006 to 2017. Transbound Emerg Dis 66:611–616CrossRef

37.

Tan CY, Opaskornkul K, Thanawongnuwech R, Arshad SS, Hassan L, Ooi PT (2020) First molecular detection and complete sequence analysis of porcine circovirus type 3 (PCV3) in Peninsular Malaysia. PLoS ONE 15:e0235832CrossRef

38.

Nguyen NH, Do Tien D, Nguyen TQ, Nguyen TT, Nguyen MN (2021) Identification and whole-genome characterization of a novel Porcine Circovirus 3 subtype b strain from swine populations in Vietnam. Virus Genes 57:385–389CrossRef

Titel: Evidence of coinfection of pigs with African swine fever virus and porcine circovirus 2
verfasst von: William G. Dundon
Giovanni Franzo
Tirumala B. K. Settypalli
N.L.P. Indi Dharmayanti
Ulaankhuu Ankhanbaatar
Indrawati Sendow
Atik Ratnawati
Tserenchimed Sainnokhoi
Umberto Molini
Giovanni Cattoli
Charles E. Lamien
Publikationsdatum: 26.11.2021
Verlag: Springer Vienna
Erschienen in: Archives of Virology / Ausgabe 1/2022
Print ISSN: 0304-8608
Elektronische ISSN: 1432-8798
DOI: https://doi.org/10.1007/s00705-021-05312-7

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Evidence of coinfection of pigs with African swine fever virus and porcine circovirus 2

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