Tomlinson Joy E, Kapoor Amit, Kumar Arvind, Tennant Bud C, Laverack Melissa A, Beard Laurie, Delph Katie, Davis Elizabeth, Schott Ii Harold, Lascola Kara, Holbrook Todd C, Johnson Philip, Taylor Sandra D, McKenzie Erica, Carter-Arnold Jessica, Setlakwe Emilie, Fultz Lisa, Brakenhoff Jeff, Ruby Rebecca, Trivedi Sheetal, Van de Walle Gerlinde R, Renshaw Randall W, Dubovi Edward J, Divers Thomas J
Department of Microbiology and Immunology, Baker Institute for Animal Health, College of Veterinary Medicine, Cornell University, Ithaca, New York.
Center for Vaccines and Immunity, Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
J Vet Intern Med. 2019 Jan;33(1):251-257. doi: 10.1111/jvim.15368. Epub 2018 Dec 5.
Three flaviviruses (equine pegivirus [EPgV]; Theiler's disease-associated virus [TDAV]; non-primate hepacivirus [NPHV]) and equine parvovirus (EqPV-H) are present in equine blood products; the TDAV, NPHV, and EqPV-H have been suggested as potential causes of serum hepatitis.
To determine the prevalence of these viruses in horses with equine serum hepatitis.
Eighteen horses diagnosed with serum hepatitis, enrolled from US referral hospitals.
In the prospective case study, liver, serum, or both samples were tested for EPgV, TDAV, NPHV, and EqPV-H by PCR.
Both liver tissue and serum were tested for 6 cases, serum only for 8 cases, and liver only for 4 cases. Twelve horses received tetanus antitoxin (TAT) 4-12.7 weeks (median = 8 weeks), 3 horses received commercial equine plasma 6-8.6 weeks, and 3 horses received allogenic stem cells 6.4-7.6 weeks before the onset of hepatic failure. All samples were TDAV negative. Two of 14 serum samples were NPHV-positive. Six of 14 serum samples were EPgV-positive. All liver samples were NPHV-negative and EPgV-negative. EqPV-H was detected in the serum (N = 8), liver (N = 4), or both samples (N = 6) of all 18 cases. The TAT of the same lot number was available for virologic testing in 10 of 12 TAT-associated cases, and all 10 samples were EqPV-H positive.
We demonstrated EqPV-H in 18 consecutive cases of serum hepatitis. EPgV, TDAV, and NPHV were not consistently present. This information should encourage blood product manufacturers to test for EqPV-H and eliminate EqPV-H-infected horses from their donor herds.
三种黄病毒(马pegivirus [EPgV];泰勒氏病相关病毒[TDAV];非灵长类肝炎病毒[NPHV])和马细小病毒(EqPV-H)存在于马血液制品中;TDAV、NPHV和EqPV-H被认为是血清性肝炎的潜在病因。
确定这些病毒在患马血清性肝炎马匹中的流行情况。
从美国转诊医院招募的18匹被诊断为血清性肝炎的马。
在这项前瞻性病例研究中,通过聚合酶链反应(PCR)检测肝脏、血清或两者样本中的EPgV、TDAV、NPHV和EqPV-H。
6例同时检测了肝脏组织和血清,8例仅检测了血清,4例仅检测了肝脏。12匹马在肝衰竭发作前4至12.7周(中位数=8周)接受了破伤风抗毒素(TAT),3匹马在6至8.6周接受了商业马血浆,3匹马在6.4至7.6周接受了同种异体干细胞。所有样本TDAV均为阴性。14份血清样本中有2份NPHV呈阳性。14份血清样本中有6份EPgV呈阳性。所有肝脏样本NPHV和EPgV均为阴性。18例病例的血清(N = 8)、肝脏(N = 4)或两者样本(N = 6)中均检测到EqPV-H。12例与TAT相关的病例中有10例可获得相同批号的TAT用于病毒学检测,所有10份样本EqPV-H均呈阳性。
我们在18例连续的血清性肝炎病例中证实了EqPV-H的存在。EPgV、TDAV和NPHV并非始终存在。这些信息应促使血液制品制造商检测EqPV-H,并将感染EqPV-H的马匹从供血马群中剔除。