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Abstract

A nanocrystalline Ti alloy powder was fabricated using cryomilling. The grain size and lattice strain evolution during cryomilling were quantitatively analyzed using X-ray diffraction (XRD) based on the Scherrer equation, Williamson-Hall (W-H) plotting method, and size-strain (S-S) method assuming uniform deformation. Other physical parameters including stress and strain have been calculated. The average crystallite size and the lattice strain evaluated from XRD analysis are in good agreement with the result of transmission electron microscopy (TEM).

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Authors and Affiliations

M. Oh
H.K. Yu
J.-H. Lee
M.C. Oh
S.-H. Jung
B. Ahn
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Abstract

In the current study, twenty lambs, aged 4 months, half male and half female, were classified into four groups, with five in each group. The experimental three groups of lambs were given intravenous (IV), intramuscular (IM) and subcutaneous (SC) administrations of recombinant ovine interferon-τ (roIFN-τ). The fourth group (normal control) of lambs was given normal saline injections in the same way. After administrations, blood samples were collected from the tested animals at different time points post injection, and the serum titers of roIFN-τ were measured using cytopathic effect (CPE) inhibition bioassay. The results of calculating pharmacokinetic (PK) parameters using DAS software showed that the PK characteristics of roIFN-τ through IV injection conformed to the two-compartment open model, whose half-life of distribution phases (T1/2α) was 0.33±0.034 h and the elimination half-life(T1/2β) was 5.01±0.24 h. However, the PK features of IM injection and SC injection of roIFN-τ conformed to the one compartment open model, whose Tmax were 3.11±0.26 h and 4.83±0.43 h, respectively, together with an elimination half life(T1/2β) of 9.11±0.76 h and 7. 43±0.58 h, and an absorption half-life (T1/2k(a)) of 1.13±0.31 h and 1.85±0.40 h, respectively. The bioavailability of roIFN-τ after IM administration reaches 73.57%, which is greater than that of SC administration (53.43%). These results indicate that the drug administration effect can be preferably obtained following a single dose IM administration of the roIFN-τ aqueous preparation. This study will facilitate the clinical application of roIFN-τ as a potential antiviral agent in future work.

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Authors and Affiliations

J. Zhao
H.Y. Yu
Y. Zhao
S.Q. Li
X.L. Fu
W. Zhou
B.B. Xia
M.L. Wang
J. Chen
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Abstract

Classical swine fever (CSF) and porcine reproductive and respiratory syndrome (PRRS) are responsible for major economic losses and represent a threat to the swine industry worldwide. Routine surveillance serology for CSF and PRRS viruses is critical to maintaining the health status of sow farms in Hunan Province, which is one of the top pig production provinces in China. The aim of our study was to investigate the serological statistics of CSF virus (CSFV) and PRRS virus (PRRSV) in Hunan Province. The cohort serum samples were collected from vaccinated and unvaccinated pigs. Our findings showed that the average rates of CSFV and PRRSV antibody seropositivity were 82.2% (95% CI: 80.1-84.3) and 84.8% (95% CI: 82.5-87.1), respectively, in the immunized group and that these rates were higher than those in the unvaccinated group (58.6% for CSFV and 47.8% for PRRSV). Additionally, the level of CSFV antibody in piglet serum declined gradually with age, whereas PRRSV-specific antibody level increased initially (1 to 2 weeks old) and then declined with age (2 to 4 weeks old). In summary, we investigated the difference in CSFV/PRRSV antibody levels among piglets at various weeks old (1 to 4 weeks) to further establish the duration of maternal immunity in piglets. In addition, routine monitoring of CSFV/PRRSV antibodies in immunized pigs was carried out to evaluate the efficacy of vaccination.
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Bibliography


Brown VR, Bevins SN (2018) A Review of Classical Swine Fever Virus and Routes of Introduction into the United States and the Potential for Virus Establishment. Front Vet Sci 5: 31.
Chae C (2021) Commercial PRRS Modified-Live Virus Vaccines. Vaccines (Basel) 9: 185.
Deka D, Barman NN, Deka N, Batth BK, Singh G, Singh S, Agrawal RK, Mukhopadhyay CS, Ramneek (2021) Sero-epidemiology of por-cine parvovirus, circovirus, and classical swine fever virus infections in India. Trop Anim Health Prod 53: 180.
Farsang A, Lévai R, Barna T, Fábián K, Blome S, Belák K, Bálint Á, Koenen F, Kulcsár G (2017) Pre-registration efficacy study of a novel marker vaccine against classical swine fever on maternally derived antibody positive (MDA+) target animals. Biologicals 45: 85-92.
Gao JC, Xiong JY, Ye C, Chang XB, Guo JC, Jiang CG, Zhang GH, Tian ZJ, Cai XH, Tong GZ, An TQ (2017) Genotypic and geographical distribution of porcine reproductive and respiratory syndrome viruses in mainland China in 1996-2016. Vet Microbiol 208: 164-172.
Gong W, Li J, Wang Z, Sun J, Mi S, Lu Z, Cao J, Dou Z, Sun Y, Wang P, Yuan K, Zhang L, Zhou X, He S, Tu C (2019) Virulence evalua-tion of classical swine fever virus subgenotype 2.1 and 2.2 isolates circulating in China. Vet Microbiol 232: 114-120.
Goraya MU, Ziaghum F, Chen S, Raza A, Chen Y, Chi X (2018) Role of innate immunity in pathophysiology of classical swine fever virus infection. Microb Pathog 119: 248-254.
Guo Z, Chen XX, Li R, Qiao S, Zhang G (2018) The prevalent status and genetic diversity of porcine reproductive and respiratory syndrome virus in China: a molecular epidemiological perspective. Virol J 15: 2.
Han M, Yoo D (2014) Engineering the PRRS virus genome: updates and perspectives. Vet Microbiol 174: 279-295.
Luo Y, Li S, Sun Y, Qiu HJ (2014) Classical swine fever in China: a minireview. Vet Microbiol 172: 1-6.
Madapong A, Saeng-Chuto K, Chaikhumwang P, Tantituvanont A, Saardrak K, Pedrazuela Sanz R, Miranda Alvarez J, Nilubol D (2020) Immune response and protective efficacy of intramuscular and intradermal vaccination with porcine reproductive and respiratory syndrome vi-rus 1 (PRRSV-1) modified live vaccine against highly pathogenic PRRSV-2 (HP-PRRSV-2) challenge, either alone or in combination with of PRRSV-1. Vet Microbiol 244: 108655.
Montaner-Tarbes S, Del Portillo HA, Montoya M, Fraile L (2019) Key Gaps in the Knowledge of the Porcine Respiratory Reproductive Syndrome Virus (PRRSV). Front Vet Sci 6: 38.
Stoian AM, Rowland RR (2019) Challenges for Porcine Reproductive and Respiratory Syndrome (PRRS) Vaccine Design: Reviewing Virus Glycoprotein Interactions with CD163 and Targets of Virus Neutralization. Vet Sci 6: 9.
Suradhat S, Damrongwatanapokin S, Thanawongnuwech R (2007) Factors critical for successful vaccination against classical swine fever in endemic areas. Vet Microbiol 119: 1-9.
VanderWaal K, Deen J (2018) Global trends in infectious diseases of swine. Proc Natl Acad Sci USA 115: 11495-11500.
Yin B, Qi S, Sha W, Qin H, Liu L, Yun J, Zhu J, Li G, Sun D (2021) Molecular Characterization of the Nsp2 and ORF5 (ORF5a) Genes of PRRSV Strains in Nine Provinces of China During 2016-2018. Front Vet Sci 8: 605832.
Zhang H, Leng C, Tian Z, Liu C, Chen J, Bai Y, Li Z, Xiang L, Zhai H, Wang Q, Peng J, An T, Kan Y, Yao L, Yang X, Cai X, Tong G (2018) Complete genomic characteristics and pathogenic analysis of the newly emerged classical swine fever virus in China. BMC Vet Res 14: 204.
Zhou B (2019) Classical Swine Fever in China-An Update Minireview. Front Vet Sci 6: 187.
Zhou L, Ge X, Yang H (2021) Porcine Reproductive and Respiratory Syndrome Modified Live Virus Vaccine: A “Leaky” Vaccine with Debatable Efficacy and Safety. Vaccines (Basel) 9: 362.
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Authors and Affiliations

H. Yu
1
L. Zhang
1
Y. Cai
1
Z. Hao
2
Z. Luo
3
T. Peng
1
L. Liu
N. Wang
1
G. Wang
1
Z. Deng
1
Y. Zhan
1

  1. Provincial Key Laboratory of Protein Engineering in Animal Vaccines, Research Center of Reverse Vaccinology (RCRV), and Laboratory of Functional Proteomics (LFP), College of Veterinary Medicine, Hunan Agricultural University, Changsha, Hunan 410128, China
  2. Yongzhou Animal Husbandry and Aquatic Affairs Center, Yongzhou, Hunan 425000, China
  3. Dingcheng Animal Husbandry and Aquatic Affairs Center, Changde, Hunan 415100, China

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