Journal for Veterinary Medicine, Biotechnology and Biosafety
Volume
11, Issue 1, January 2025, Pages 39–49
ISSN 2411-3174 (print version) ISSN 2411-0388
(online version)
VIROPHORY
OF THE PIG’S MICROFLORA AS A PHENOMENON OF THE SOME PORCINE VIRAL
INFECTIONS PERENNISATION
Buzun A. I. 1,
Kolchyk O. V. 1,
Rudenko Ye. V. 1,
Fotina T. I. 2,
Pass S. V. 3
1 National Scientific
Center ‘Institute of Experimental and Clinical Veterinary
Medicine’, Kharkiv, Ukraine, e-mail: kolchyk-elena@ukr.net
2 Sumy National
Agrarian University, Sumy, Ukraine
3 Veterinary clinic
‘Optim-Vet’ Ltd, Kamianske, Dnipropetrovsk Region, Ukraine
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PDF (print version)
Citation for print version: Buzun, A. I., Kolchyk, O. V., Rudenko, Ye. V.,
Fotina, T. I. and Pass, S. V.
(2025) ‘Virophory of the
pig’s microflora as a phenomenon of the some porcine viral infections
perennisation’, Journal
for Veterinary Medicine, Biotechnology and Biosafety, 11(1),
pp. 39–49.
Download
PDF (online version)
Citation for online version: Buzun, A. I., Kolchyk, O. V., Rudenko, Ye. V.,
Fotina, T. I. and Pass, S. V.
(2025) ‘Virophory of the
pig’s microflora as a phenomenon of the some porcine viral infections
perennisation’, Journal
for Veterinary Medicine, Biotechnology and Biosafety,
11(1), pp. 39–49. DOI: 10.36016/JVMBBS-2025-11-1-6.
Summary. The problem of the
perennisation porcine viral infections/rooting their agents is far from clear
understanding. The article proposes a mechanism for the rooting of porcine
viral infections through the interaction of viruses with the porcine
microbiome. This provision is standed on results of retrospectively examine the
relationship between bacterial virophoria of the primary microbiological
cultures and the enzootic foci formation on the model of two enzootic focies of
porcine respiratory disease complex (PRDC) with including of agents of the
Aujeszky’s disease (AD) and porcine circovirus infection (PCVI). There
was studied 183 samples of primary bacterial cultures (BC) from samples of
clinical and pathological materials taken from pigs during the outbreaks/‘PRDC
red phases’ (‘exposed pigs’) and in ‘PRDC green
phases’ (‘non-exposed pigs’). There AD agent virophoria
detected in 29 bacterial samples (70.7%, BC from nasal mucus, semen, liver
and spleen) and PCVI agent ― in 22 samples (59.5%, BC from
nasal and vaginal mucus and lungs) were recorded in group of ‘exposed
pigs’. But there only 5 from 142 bacterial samples (3.5%, BC
exclusively in semen samples) was recorded in group of ‘unexposed
pigs’ in both holdings as virophoric for AD agent and two from
20 samples as virophoric for PCV-2 (11.1%, BC from lung and vaginal mucus
samples). In according EvansCounty calculation (Epi Info for Windows
v. 7.1.5) these date did next significance odds rations (OR) and risk
ration (RR) indexes (P = 99.99%):
16.12 ≤ OR = 43.17 ≤ 134.05 and
3.13 ≤ RR = 4.25 ≤ 5.77,
respectively. In addition, there BC from 11 nasal swabs of pigs with
clinical signs of PRDC in back-yard holdings after the lifting of the
quarantine for African swine fever (ASF) was examined in PCR on ASF. The
5 BC samples revealed as virophoric. To further develop of the Kharkiv
doctrine of the associated infections epizootiology the concept of switching
the epidemic process into an endemic one in piggery through the direct
interaction of viruses with the pig microbiome is proposed
Keywords: Aujeszky’s
disease, porcine circoviral disease, African swine fever
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