- Research article
- Open Access
Change in the responsiveness of interferon-stimulated genes during early pregnancy in cows with Borna virus-1 infection
BMC Veterinary Researchvolume 12, Article number: 253 (2016)
Borna disease virus is a neurotropic pathogen and infects the central nervous system. This virus infected a variety of animal species including cows. The most of cows infected with Borna disease virus 1 (BoDV-1) exhibit subclinical infection without any neurological symptoms throughout their lifetime. We previously reported on the low conception rates in-seropositive cows. Interferon-τ (IFN-τ) plays an important role in stable fertilization, and is produced from the fetal side following embryo growth at 15–40 days of pregnancy. IFN-τ induces the expression of interferon-stimulated gene (ISG) 15 and Mx2 in peripheral blood mononuclear cells (PBMCs). To understand the embryo growth and maternal reaction during early pregnancy in cows with BoDV-1 infection, we aimed to assess the gene expression of ISG15 and Mx2 from PBMCs in BoDV-1-seropositive cows.
None of the cows showed any clinical and neurological symptoms. Among the cows that conceived, the expressions of the ISG15 and Mx2 genes were greater in the BoDV-1-seropositive cows than in the BoDV-1-seronegative cows; the difference was significant between the cows that conceived and those that did not (P < 0.05).
The expression of ISG15 and Mx2 genes during early pregnancy significantly increased in the BoDV-1-seropositive cows and may be important for the maintenance of stable pregnancy in BoDV-1-infected cows. In contrast, the gene expression levels of ISG15 and Mx2 did not significantly increase during early pregnancy in BoDV-1-seronegative cows. Thus, BoDV-1 infection may lead to instability in the maintenance of early pregnancy by interfering with INF-τ production.
Borna disease virus is a negative single-stranded RNA virus that was first identified in Germany . The potential hosts for the virus widely range from birds to non-human primates, such as cattle, sheep, rodent and horse [1–4]. The BoDV-1 is a neurotropic pathogen that infects the central nervous system. Several cases of borna disease virus 1(BoDV-1) infection have been reported in Japanese cows, most of which exhibited subclinical infection without any neurological symptoms. Moreover, we previously reported a decrease in the conception rate in BoDV-1 antibody-positive dairy cows. Although ovulation and estrus at the time of artificial insemination (AI) were normal, BoDV-1 antibody-positive cows required repeated insemination and showed a significant increase in the calving-to-conception interval .
Interferon (IFN)-τ is a type 1 IFN produced by the conceptus from the fetal side at 15–40 days of pregnancy. It plays an important role in fertilization; in fact, pregnancy can be maintained by suppressing the production of luteolytic pulses of Prostaglandin (PG)-F2α by the endometrium to maintain corpora lutea and their production of P4, the unequivocal hormone of pregnancy [6–8]. IFN-τ doesn’t stimulate interferon stimulated gene (ISG), such as ISG15 and Mx2 in maternal Luminal epithelium and superficial glands. IFN-τ down regulated oxytocin receptor through IRF-2. In pregnant ovine, exsomes stimulate trophecderm cells to proliferate and secrete IFN-τ with regulation of TLR- mediated cell signaling .On the other hands, IFN-τ stimulated ISG through STAT1, STAT2 and IRF9 in immune cells like a PBMCs . IFN-τ induce ISG15, Mx1, Mx2, and OAS1 in PBMCs [10–13]. The production of IFN-τ is low limited and is rapidly eliminated from the mother, it is difficult to directly measure the IFN-τ levels from the serum samples of pregnant mothers. Hence, IFN-τ production can be indirectly estimated by measuring the expression of interferon-stimulated genes (ISG) or Mx levels from maternal mononuclear cells . Thus, the levels of ISG15 and Mx2 could serve as an indicator of the maternal conception status during early pregnancy [8, 13, 15]. Moreover, this type 1 IFN has anti-viral activity [8, 16–18]. On the contrary, BoDV-1 inhibits type 1 interferon induction through interferon regulatory factor (IRF) 3 and 7 pathway . In the present study, to understand the embryo growth and maternal reaction to IFN-τ during early pregnancy in cows infected with BoDV-1, we examined the gene expression of ISG15 and Mx2 from PBMCs in BoDV-1 infected cows.
We examined a total of 58 multiparous Holstein Friesian cows. All the cows were confirmed to be clinically healthy during the experimental period and did not have a history of treatment for reproductive difficulties prior to the experiment. The examined cows were similarly managed in the farm and received the same programmed feeding. AI was conducted in dried multiparous cows during standing estrus, and the same practitioner performed ovarian inspection via rectal examination. The blood samples were collected from the cows two times before and after AI at approximately 18–25 days; the PBMC fraction was then separated using the Ficoll-Conray centrifugation method (density, 1.086). Early pregnancy status was confirmed in all the cows via a rectal ultrasound scan of the uterus at 30–45 days after AI. The study was covered by approval of the Ethics Committee of the School of Veterinary Medicine, Rakuno Gakuen University in Japan.
RNA was extracted from the PBMCs and cDNA was synthesized using anchored-oligo (dT) 18 primer (Transcriptor First Strand cDNA Synthesis Kit, Roche). The expression of ISG15 and Mx2 genes was examined using quantitative RT-PCR (LightCycler® FastStart DNA Master SYBR Green I, Roche); the gene expression was normalized to GAPDH . The primer pairs for the detection of the genes are as follows—ISG15 (NM_174366) forward: GGTATCCGAGCTGAAGCAGTT, reverse: ACCTCCCTGCTGTCAAGGT (131–217, 86 bp); Mx2 (NM_173941) forward: CTTCAGAGACGCCTCAGTCG, reverse: TGAAGCAGCCAGCAATAGTG (2071–2302, 231 bp); and GAPDH (XR_082746) forward: GATTGTCAGCAATGCCTCCT, reverse: GGTCATAAGTCCCTCCACGA (546–638, 92 bp).
Detection of BoDV-1 antibody
Anti-BoDV-1 antibodies were detected using western blotting, with the recombinant BoDV-1 nucleoprotein antigen [20, 21]. Serum samples were diluted at 1:100 with phosphate-buffered saline containing 10% Block Ace (Dainippon Pharmaceutical Co., Osaka, Japan) and 0.05% Tween 20, and western blotting assays were performed. Antibody-antigen complexes were identified using peroxidase-conjugated goat affinity-purified anti-bovine IgG. The obtained antibody findings were compared with the change in the gene expression of the ISG15 and Mx2.
The statistical analysis of BoDV-1 infected cows between conception and conception failure determined by using Chi-square test. Significant differences in the expressions of the ISG15 and Mx2 genes were assayed using one-way analysis of variance. The ISG15 and Mx2 gene expression ratio calculated after AI value/before AI value. The change in the ratio of gene expression between cows that conceived and cows with conception failure was determined by using Student’s t-test.
The BoDV-1 antibody examination indicated that 38 of 58 cows were seropositive, as shown in Table 1. The same practitioner conducted AI on dried multiparous cows during standing estrus as well as ovarian inspection via rectal examination; all the cows showed a clear estrus for ovulation without any clinical problems.
A total of 20 cows exhibited seronegative negative results; of these cows, 11 were pregnant after AI and nine had conception failure (conception rate, 55%). In contrast, the conception rate was 39.5% in seropositive cows, including 15 cows that conceived and 23 cow that had conception failure. There were no significantly deference conception between BoDV-1 infected cows and uninfected cows. All the cows were clinically normal and none showed any clinical symptoms, such as those accompanying BoDV-1 infection cases, including neurological symptoms. Blood examination data indicated normal parameters in all the cows during the observation period.
The ratio of gene expression was evaluated between two blood-sampling points: before AI and after 18-25 days AI treatment. Among the seropositive cows, the gene expression rate of ISG15 was 8.5 times significantly higher in the cows that conceived as compared to the cows with conception failure (Fig. 1, p = 0.0008). The gene expression of Mx2 was also significantly greater (4.5 times) in the conceived cows (Fig. 2, p = 0.002). In contrast, among the seronegative cows, the ISG15 and Mx2 gene expression levels in the cows that conceived were only slightly greater than those in the cows with conception failure (Figs. 1 and 2). The gene expression levels of ISG15 and Mx2 after AI were higher in the seropositive cows that conceived than in the cows with conception failure; these levels were significantly different between the cows that conceived and those that did not conceive (P < 0.05).
ISG15 is produced from the mononuclear cells in the mother in response to stimulation by IFN-τ. The IFN-τ has also been observed to influence Mx2 gene expression, and the expressions of both ISG15 and Mx2 have been reported during the early stages of pregnancy [13, 15, 22]. In the BoDV-1 infected group, a significant increase in ISG15 and Mx2 expression levels was observed after conception; however, the gene expression levels only slightly increased in the BoDV-1 uninfected group. The cows infected with BoDV-1 tended to increase IFN-τ production and/or a higher response to IFN-τ during pregnancy. The secretion of IFN-τ is regulated by exsome, endogenous jaagsiekte retroviruses in ovine . BoDV-1 infection may affect on the IFN-tau expression in the embryo. The relatively higher expression of IFN-τ may be essential for ensuring stable pregnancy, and the anti-viral effect of type 1 IFN might contribute to the maintenance of pregnancy in cows infected with BoDV-1. In fact, type 1 IFN has been shown to inhibit BoDV-1 multiplication in an infected animal model . The reports has BoDV-1 down regulated secretion of type 1 IFN through IRF-3 and 7 and Avian borna virus infected cell reduced secretion of type 1 IFN. IFN-τ may be influenced the secretion in fetal side and response in BoDV-1 infected maternal cows [6, 24].
In the present study, we confirmed that the expressions of ISG15 and Mx2 genes were enhanced in cows infected with BoDV-1. Although the levels of type 1 IFN from PBMCs in infected cows have not been investigated, a higher response to IFN-τ and/or increased IFN-τ production during early pregnancy may be important for maintaining pregnancy in cows infected with BoDV-1. Thus, BoDV-1 infection could affect the fecundity and maintenance of pregnancy. Therefore, the conception and maintenance of early pregnancy appears to require a higher response of ISG15 and Mx2 to IFN stimulation in cows infected with BoDV-1. The PBMCs from BoDV-1 infected cows have a clear response to IFN-τ stimulation.
Moreover, BoDV-1 infection may lead to difficulties in conception and maintenance of pregnancy; in these cases, the host may need to produce a greater IFN reaction to overcome this limitation. Repeated insemination and a significant increase in the calving-to-conception interval at BoDV-1 infected cows may relate to change of responsiveness for type 1 IFN. Hence, pregnancy and IFN production should be examined in detail in infected cows in future studies.
In conclusion, BoDV-1 infection may lead to instability in the maintenance of early pregnancy by interfering with IFN-τ production. BoDV-1 infected dairy cows were lower conception rate than BoDV-1 uninfected cows. The expression of ISG15 and Mx2 during early pregnancy significantly increased in the BoDV-1-infected cows. But in the BoDV-1 uninfected cows did not. Hence, the conception and maintenance of early pregnancy appears to require a higher production of IFN-τ in cows infected with BoDV-1.
Borna disease virus-1
Interferon regulatory factor
Myxovirus resistance gene
Oligoadenylate synthetase 1
Peripheral blood mononuclear cells
Signal transducers and activator of transcription
Toll like receptor
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We would thank Yuko Kato-Mori and Shin Yoshinaga for assistance with technical supports and collection of samples. We would like to thank Editage (www.editage.jp) for English language editing.
This study was supported, in part, by the Grants-in-Aid for Science Research JSPS KAKENHI Grant Number 23580427, 26292160, 25292182.
Availability of data and materials
All data supporting the results of this study are included within the article.
TT and KH conducted the molecular genetic studies, participated in the quantitative RT-PCR, and drafted the manuscript. TT and TO conducted the immunoassays. TA participated in sample collection. KH participated in study design and performed statistical analysis. TT and KH conceived of the study, participated in its design and coordination, and helped to draft the manuscript. All authors read and approved the final manuscript.
The author declare that they have no competing interests.
Consent for publication
This study was covered by approval of the Ethics Committee of the School of Veterinary Medicine, Rakuno Gakuen University in Japan (approval number: VH22A15). This study did not include animal experiments. The owners consented to the use and disclosure of questionnaire data for current study.