Molecular detection, histopathological analysis, and immunohistochemical characterization of equine infectious anemia virus in naturally infected equids.

Equine infectious anemia (EIA), a disease caused by equine infectious anemia virus (EIAV), is considered an obstacle to the development of the horse industry. There is no treatment or vaccine available for EIA, and its pathogenesis, as well as the immune response against the virus, is not fully understood. Therefore, an immunohistochemistry assay was developed for the detection of viral antigens in tissues of equids naturally infected with EIAV. Sections of organs of six equids from Apodi-RN, Brazil, that tested positive for EIA by serological tests (ELISA and AGID) were fixed in 10% formalin solution and embedded in paraffin. Immunohistochemistry was performed using a polyclonal anti-EIAV antibody. EIAV antigens were observed in red spleen pulp cells and hepatic sinusoids, as well as bronchiolar and alveolar epithelial cells of the lungs and proximal and distal tubules of the kidneys. The presence of EIAV in the spleen and liver was expected due to viral tropism by macrophages, which are abundantly present in these organs. However, EIAV was also found in lung and kidney epithelial cells, indicating that the virus infects cell types other than macrophages. In conclusion, the immunohistochemical assay standardized in this study was able to detect EIAV antigens in spleen, liver, kidney and lung cells from naturally infected EIAV equids. Immunostaining observed in the spleen confirms viral tropism by mononuclear phagocytes; however, the presence of EIAV in lung and kidney epithelial cells indicates that virus may be eliminated in urine and/or oronasal secretions, suggesting new routes for viral excretion.

[Equine Infectious Anaemia - a review from an official veterinary perspective]. / Die Equine Infektiöse Anämie ­ eine Besprechung aus amtstierärztlicher Sicht.

INTRODUCTION: Equine infectious anaemia (EIA) is a sporadic viral disease in many countries. Every single case has, however, a dramatic impact: infected animals have to be put down, and quarantine restrictions on horse movements lasting three months lead to substantial economic losses. In Switzerland, the mandatory notification was introduced in 1994 in order to facilitate international traffic. A year later, the "new" Ordinance on epizootics of 1995 classified EIA as a "disease to be eradicated". An infected polo horse in the canton of Argovia in summer 2017 thus represented Switzerland's first official case. It served as a starting point to review the legal frameworks of the EU and Switzerland. Recent publications suggest that there might be some potential to optimize the current diagnostic protocols. EIA is transmitted by virus-containing blood and blood products. Introductions in previously disease-free regions are mostly due to human activities, while blood feeding insects as horse flies or other biting flies act as mechanical vectors only locally within some 100 meters. As before, the new EU Regulations governing animal health do not prescribe national monitoring and control plans, allowing member states to shape them according to their particular situation. However, they have to ensure that equids intended for intracommunity movements comply with specific guarantees. In this context, a fine-tuning of current international standards seems conceivable. Mandatory testing preceding each movement would not be a proportionate option even for the future. Regardless their final wording, it would be a great step for all the actors involved in animal traffic if it were possible to adopt rules that are accepted and uniformly implemented by all competent authorities at national, regional and local level. However, the official system will never be able to guarantee absolute safety. Since there are neither effective vaccines nor treatment protocols, it is crucial that all owners, stablehands, veterinarians, associations, and organizers of horse contests are aware of the disease risks, minimizing them as far as possible by adequate biosecurity measures.

INTRODUCTION: L'anémie infectieuse des équidés (AIE) est une maladie virale sporadique dans de nombreux pays. Chaque cas a pourtant de graves conséquences: les animaux infectés doivent être éliminés, et les interdictions de mouvements d'équidés pendant trois mois causent des pertes économiques substantielles. En Suisse, la notification obligatoire a été introduite en 1994 pour faciliter les échanges transfrontaliers. En 1995, la «nouvelle¼ ordonnance sur les épizooties a ensuite classé l'AIE dans la catégorie des «épizooties à éradiquer¼. Le cheval de polo infecté, qui a été découvert durant l'été 2017 dans le canton d'Argovie, représente donc le premier cas officiel d'AIE en Suisse. Il a servi de point de départ pour une appréciation de la réglementation de l'UE et du droit suisse. Des études récentes indiquent qu'il existerait un potentiel d'optimisation des protocoles de diagnostic. L'AIE est transmise par le sang et les produits sanguins contenant l'agent infectieux. L'introduction de la maladie dans une région indemne est souvent liée à des activités humaines, les insectes hématophages, comme les taons ou les mouches piquantes, peuvent servir de vecteurs mécaniques au niveau local, dans un rayon ne dépassant pas quelques centaines de mètres. Comme l'actuelle, la nouvelle réglementation de l'UE régissant la santé animale ne prescrira pas aux États membres une stratégie nationale de surveillance ou de lutte, qu'ils peuvent en conséquence adapter en fonction de leur situation particulière. Ils doivent toutefois assurer que les équidés destinés aux mouvements intracommunautaires remplissent des conditions spécifiées. A cet égard, un «ajustage¼ des normes internationales parait envisageable, mais comme c'est déjà le cas actuellement, un examen de laboratoire avant tout déplacement ne sera pas exigé. Indépendamment de leur formulation finale, des conditions de déplacement d'équidés généralement acceptées et appliquées uniformément par toutes les autorités compétentes aux échelles nationales, régionales et locales signifieraient un grand progrès pour tous les acteurs impliqués dans le trafic d'animaux. Les législations ne pourront jamais garantir une sécurité absolue. Considérant qu'il n'existe ni vaccination efficace ni traitement, il est crucial que les détenteurs, palefreniers, vétérinaires, associations et organisateurs de manifestations équestres soient conscients du danger d'épizootie, et qu'ils le réduisent autant que possible par des mesures de biosécurité adéquates.

Attenuation of Equine Lentivirus Alters Mitochondrial Protein Expression Profile from Inflammation to Apoptosis.

Equine infectious anemia virus (EIAV) is an equine lentivirus similar to HIV-1, targets host immune cells, and causes a life-long infection in horses. The Chinese live EIAV vaccine is attenuated from long-term passaging of a highly virulent strain in vitro The parent pathogenic strain (EIAVDLV34) induces a host inflammatory storm to cause severe pathological injury of animals. However, the vaccine strain (EIAVDLV121) induces a high level of apoptosis to eliminate infected cells. To investigate how these processes are regulated, we performed a comparative proteomics analysis and functional study in equine monocyte-derived macrophages (eMDMs) and found that the divergent mitochondrial protein expression profiles caused by EIAV strains with different virulence led to disparate mitochondrial function, morphology, and metabolism. This in turn promoted the distinct transformation of macrophage inflammatory polarization and intrinsic apoptosis. In EIAVDLV34-infected cells, a high level of glycolysis and increased mitochondrial fragmentation were induced, resulting in the M1-polarized proinflammatory-type transformation of macrophages and the subsequent production of a strong inflammatory response. Following infection with EIAVDLV121, the infected cells were transformed into M2-polarized anti-inflammatory macrophages by inhibition of glycolysis. In this case, a decrease in the mitochondrial membrane potential and impairment of the electron transport chain led to increased levels of apoptosis and reactive oxygen species. These results correlated with viral pathogenicity loss and may help provide an understanding of the key mechanism of lentiviral attenuation.IMPORTANCE Following viral infection, the working pattern and function of the cell can be transformed through the impact on mitochondria. It still unknown how the mitochondrial response changes in cells infected with viruses in the process of virulence attenuation. EIAVDLV121 is the only effective lentiviral vaccine for large-scale use in the world. EIAVDLV34 is the parent pathogenic strain. Unlike EIAVDLV34-induced inflammation storms, EIAVDLV121 can induce high levels of apoptosis. For the first time, we found that, after the mitochondrial protein expression profile is altered, EIAVDLV34-infected cells are transformed into M1-polarized-type macrophages and cause inflammatory injury and that the intrinsic apoptosis pathway is activated in EIAVDLV121-infected cells. These studies shed light on how the mitochondrial protein expression profile changes between cells infected by pathogenic lentivirus strains and cells infected by attenuated lentivirus strains to drive different cellular responses, especially from inflammation to apoptosis.

Infection with equine infectious anemia virus vaccine strain EIAVDLV121 causes no visible histopathological lesions in target organs in association with restricted viral replication and unique cytokine response.

The live equine infectious anemia virus (EIAV) vaccine strain EIAVDLV121 was developed by in vitro attenuation of a virulent strain, EIAVLN40, in the 1970s, and it has been demonstrated to induce protective immunity under laboratory and natural EIAV infection conditions. The detailed biological features of this attenuated virus remain to be further investigated. Experimental inoculation with EIAVDLV121 did not result in clinical symptoms even with immunosuppressive treatment in our previous studies. Here, we further investigated whether the replication of the vaccine strain EIAVDLV121 in experimentally infected horses causes histopathological lesions to develop in the targeted organs. Both the lungs and the spleen have been demonstrated to support EIAV replication. By evaluating the gross macroscopic and histological changes, we found that EIAVDLV121 did not cause detectable histopathological lesions and that it replicated several hundred times more slowly than its parental virulent strain, EIAVLN40, in tissues. Immunochemical assays of these tissues indicated that the primary target cells of EIAVDLV121 were monocytes/macrophages, but that EIAVLN40 also infected alveolar epithelial cells and vascular endothelial cells. In addition, both of these viral strains promoted the up- and down-regulation of the expression of various cytokines and chemokines, implicating the potential involvement of these cellular factors in the pathological outcomes of EIAV infection and host immune responses. Taken together, these results demonstrate that the EIAV vaccine strain does not cause obvious histopathological lesions or clinical symptoms and that it induces a unique cytokine response profile. These features are considered essential for EIAVDLV121 to function as an effective live vaccine.

Mice transgenic for equine cyclin T1 and ELR1 are susceptible to equine infectious anemia virus infection.

BACKGROUND: As a member of the tumor necrosis factor receptor (TNFR) protein superfamily, equine lentivirus receptor 1 (ELR1) has been shown to be expressed in various equine cells that are permissive for equine infectious anemia virus (EIAV) replication. The EIAV Tat protein (eTat) activates transcription initiated at the viral long terminal repeat (LTR) promoter through a unique mechanism that requires the recruitment of the equine cyclin T1 (eCT1) cofactor into the viral TAR RNA target element. In vitro studies have demonstrated that mouse fibroblast cell lines (e.g., NIH 3T3 cells) that express the EIAV receptor ELR1 and eCT1 support the productive replication of EIAV. Therefore, we constructed transgenic eCT1- and ELR1-expressing mice to examine whether they support in vivo EIAV replication. FINDINGS: For the first time, we constructed mice transgenic for ELR1 and eCT1. Real-time reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis confirmed that ELR1 and eCT1 were expressed in the transgenic mouse tissues, particularly in the intestines, spleen and lymph nodes. Consistent with the results of EIAV infection in NIH 3T3 cells expressing ELR1 and eCT1, mouse embryonic fibroblasts (MEFs) from the transgenic mice could support EIAV replication. More importantly, this virus could infect and replicate in mouse blood monocyte-derived macrophages (mMDMs). Macrophages are the principle target cell of EIAV in its natural hosts. Furthermore, after the transgenic mice were inoculated with EIAV, the virus could be detected not only in the plasma of the circulating blood but also in multiple organs, among which, the spleen and lymph nodes were the predominant sites of EIAV replication. Finally, we found that consistent with high viral replication levels, the relevant pathological changes occurred in the spleen and lymph nodes. CONCLUSIONS: Our results show that mice transgenic for ELR1 and eCT1 are susceptible to EIAV infection and replication. Further, EIAV infection can cause lesions on the spleen and lymph nodes, similar to those frequently observed in horses, the natural hosts. Therefore, ELR1 and eCT1 are essential in vivo for EIAV invasion and replication.

Interstitial lung disease associated with Equine Infectious Anemia Virus infection in horses.

EIA (Equine Infectious Anemia) is a blood-borne disease primarily transmitted by haematophagous insects or needle punctures. Other routes of transmission have been poorly explored. We evaluated the potential of EIAV (Equine Infectious Anemia Virus) to induce pulmonary lesions in naturally infected equids. Lungs from 77 EIAV seropositive horses have been collected in Romania and France. Three types of lesions have been scored on paraffin-embedded lungs: lymphocyte infiltration, bronchiolar inflammation, and thickness of the alveolar septa. Expression of the p26 EIAV capsid (CA) protein has been evaluated by immunostaining. Compared to EIAV-negative horses, 52% of the EIAV-positive horses displayed a mild inflammation around the bronchioles, 22% had a moderate inflammation with inflammatory cells inside the wall and epithelial bronchiolar hyperplasia and 6.5% had a moderate to severe inflammation, with destruction of the bronchiolar epithelium and accumulation of smooth muscle cells within the pulmonary parenchyma. Changes in the thickness of the alveolar septa were also present. Expression of EIAV capsid has been evidenced in macrophages, endothelial as well as in alveolar and bronchiolar epithelial cells, as determined by their morphology and localization. To summarize, we found lesions of interstitial lung disease similar to that observed during other lentiviral infections such as FIV in cats, SRLV in sheep and goats or HIV in children. The presence of EIAV capsid in lung epithelial cells suggests that EIAV might be responsible for the broncho-interstitial damages observed.

Equine infectious anemia and equine infectious anemia virus in 2013: a review.

A detailed description of equine infectious anemia virus and host responses to it are presented. Current control and eradication of the infection are discussed with suggestions for improvements to increase their effectiveness.

Reverse mutation of the virulence-associated S2 gene does not cause an attenuated equine infectious anemia virus strain to revert to pathogenicity.

The contribution of S2 accessory gene of equine infectious anemia virus (EIAV) to the virulence of pathogenic strains was investigated in the present study by reverse mutation of all four consensus S2 mutation sites in an attenuated EIAV proviral strain, FDDV3-8, to the corresponding sequences of a highly pathogenic strain DV117. The S2 reverse-mutated recombinant strain FDDVS2r1-2-3-4 replicated with similar kinetics to FDDV3-8 in cultivated target cells. In contrast to the results of other studies of EIAV with dysfunctional S2, reverse mutation of S2 only transiently and moderately increased the plasma viral load of inoculated horses, and induction of transient immunosuppression did not boost viral pathogenicity. In addition, inoculation of FDDVS2r1-2-3-4 induced partial protection to a challenge pathogenic virus. These results suggest that the attenuated EIAV vaccine strain with multiple mutations in multiple genes will not easily revert to a virulent phenotype.

Frequência de anemia infecciosa equina em equinos nos estados da Paraíba, Rio Grande do Norte e Ceará durante o ano de 2010 / Frequency of equine infectious anemia in equine in the states of Paraíba, Rio Grande do Norte and Ceará, Northeastern Brazil during 2010

A frequência de equinos soro-reagentes para o vírus da Anemia Infecciosa Equina (AIE) foi investigada, durante o ano de 2010, em 5615 animais originários de 209 municípios de três estados do nordeste do Brasil: Paraíba, Rio Grande do Norte e Ceará. Os soros foram examinados com o emprego do teste de imunodifusão em gel de ágar (IDGA) produzido com o antígeno p26. Dos 5615 animais examinados, 151 (2,69%) foram soropositivos. As proporções de animais reatores positivos por estado foram: Paraíba (2,86%), Rio Grande do Norte (1,29%) e Ceará (3,10%). Tomando-se por base a menor proporção de resultados positivos encontrada no estado do Rio Grande do Norte, o estado da Paraíba apresentou uma odds ratio de 2,64 (IC 95% = 1,33-5,36; p = 0,004) e o Ceará de 2,87 (IC 95% = 1,48-5,71; p = 0,001). Na Paraíba houve o registro de animais soropositivos em todos os meses do ano, com frequência mínima (0,58%) em julho e máxima (5,82%) em junho; no Rio Grande do Norte de março a maio e de julho a novembro, com variação de 0% em janeiro, fevereiro, junho e dezembro a 3,61% em maio; e no Ceará em todos os meses com frequência mínima (1,10%) em agosto e máxima (7,29%) no mês de dezembro.

During the year of 2010 the frequency of equines sero-reactants to the Infectious Anemia vírus (EIA) was investigatedin 5,615 animals originated from 209 counties of three northeastern brazilian states: Paraíba, Rio Grande do Norte and Ceará. The serum samples were examined by an agar gel immunodiffusion test (AGID) produced with p26 antigen. Of the 5,615 animals examined 151 (2.69%) were seropositive to EIA. The proportion of seroreactant animals per state were: Paraíba (2.86%), Rio Grande do Norte (1.29%) and Ceará (3.10%). Paraíba presented an odds ratio of 2.64 (95% CI = 1.33-5.36; p = 0.004), while Ceará had an odds ratio of 2.87 (95% CI = 1.48-5.71; p = 0.001) both of them compared with Rio Grande do Norte. Paraíba had seropositive animals in all months of the year, with frequency ranging from 0.58% in July to 5.82% in June; in Rio Grande do Norte from March to May and from July to November ranging from 0% in January, February, June and December to 3.61% in May; and in Ceará in all months ranging from 1.10% in August to 7.29% in December.

An attenuated EIAV vaccine strain induces significantly different immune responses from its pathogenic parental strain although with similar in vivo replication pattern.

The EIAV (equine infectious anemia virus) multi-species attenuated vaccine EIAV(DLV121) successfully prevented the spread of equine infectious anemia (EIA) in China in the 1970s and provided an excellent model for the study of protective immunity to lentiviruses. In this study, we compared immune responses induced by EIAV(DLV121) to immunity elicited by the virulent EIAV(LN40) strain and correlated immune responses to protection from infection. Horses were randomly grouped and inoculated with either EIAV(DLV121) (Vaccinees, Vac) or a sublethal dose of EIAV(LN40) (asymptomatic carriers, Car). Car horses became EIAV(LN40) carriers without disease symptoms. Two of the four Vac horses were protected against infection and the other two had delayed onset or reduced severity of EIA with a lethal EIAV(LN40) challenge 5.5 months post initial inoculation. In contrast, all three Car animals developed acute EIA and two succumbed to death. Specific humoral and cellular immune responses in both Vac and Car groups were evaluated for potential correlations with protection. These analyses revealed that although plasma viral loads remained between 10(3) and 10(5)copies/ml for both groups before EIAV(LN40) challenge, Vac-treated animals developed significantly higher levels of conformational dependent, Env-specific antibody, neutralizing antibody as well as significantly elevated CD4(+) T cell proliferation and IFN-γ-secreting CD8(+) T cells than those observed in EIAV(LN40) asymptomatic carriers. Further analysis of protected and unprotected cases in vaccinated horses identified that cellular response parameters and the reciprocal anti-p26-specific antibody titers closely correlated with protection against infection with the pathogenic EIAV(LN40). These data provide a better understanding of protective immunity to lentiviruses.

Divergence, not diversity of an attenuated equine lentivirus vaccine strain correlates with protection from disease.

We recently reported an attenuated EIAV vaccine study that directly examined the effect of lentiviral envelope sequence variation on vaccine efficacy. The study [1] demonstrated for the first time the failure of an ancestral vaccine to protect and revealed a significant, inverse, linear relationship between envelope divergence and protection from disease. In the current study we examine in detail the evolution of the attenuated vaccine strain utilized in this previous study. We demonstrate here that the attenuated strain progressively evolved during the six-month pre-challenge period and that the observed protection from disease was significantly associated with divergence from the original vaccine strain.

Patología ultraestructural del músculo gluteus medius de caballos criollos en los llanos venezolanos infectados naturalmente por el virus de la anemia infecciosa equina / Structural pathology of gluteus medius from creole horses of venezuelan plains naturally infected by equine infectious anemia virus

La Anemia Infecciosa Equina (AIE) es una enfermedad viral, de curso agudo a crónico, que afecta a los équidos en general en los llanos venezolanos. Hasta el momento, no se han analizado los posibles efectos que pueda tener la AIE sobre el músculo esquelético. En la presente investigación se realizó un estudio ultraestructural de las fibras musculares del músculo Gluteus medius, de caballos seropositivos al test de Coggins, teniendo animales seronegativos al citado test como controles de campo. Las biopsias musculares se procesaron por las técnicas convencionales de corte fino para la microscopía electrónica de transmisión. El análisis de las micrografías electrónicas de animales seropositivos mostró cambios subletales y letales. Como alteraciones subletales, se observaron en el sistema contráctil, atrofia y trazo irregular de la línea Z. En el sistema sarcotubular se evidenció edema de las cisternas terminales. Las mitocondrias exhibieron una matriz con diferentes densidades electrónicas y la presencia de gránulos electrón densos. Se observaron variadas estructuras lisosomales. Por su parte, las alteraciones letales se distinguieron por diferentes grados de hipercontracción, pérdida total de la organización de los sistemas contráctil y sarcotubular, degeneración de las mitocondrias, ruptura del sarcolema y necrosis segmental. Los capilares intramusculares exhibieron alteraciones como el engrosamiento y reduplicación de la membrana basal, prolongaciones del citoplasma endotelial hacia la luz y pérdida de la continuidad de la pared endotelial. Se evidenciaron también pericitos, unos aparentemente normales, otros con alteraciones. El infiltrado celular consistió en macrófagos y neutrófilos. Los presentes hallazgos permiten sugerir que los mismos se corresponden con lo reportado por otros autores en relación a los efectos de las enfermedades autoinmunes sobre la ultraestructura del músculo esquelético.

The equine infectious anemia (EIA) is a viral disease of acute response and progress to chronic course which affects equine of Venezuelan plains. Until now, there is no information about the possible effect of EIA on skeletal muscle ultrastructure. The aim of the present investigation was to study the ultrastructure of muscle Gluteus medius from horses positive to Coggins test and animal control negative to the test. Muscle biopsies were processed by routine techniques for transmission electron microscopy. Muscle alterations varied from slight to severe, including atrophy, swelling of sarcotubular system and mitochondria. Mitochondria showed a matrix with different electron densities and the presence of electron dense granules. There were observed different kinds of lysosomes. More severe alterations included hypercontraction and complete loss of myofilaments, rupture of sarcolemma and segmental necrosis. Intramuscular capillaries exhibited endothelial cell cytoplasm infoldings into the lumen and partially or totally occluded lumen. Basement membrane was widened and reduplicated. Some capillaries showed widened endothelial cell cytoplasm, mitochondria and rough endoplasmic reticulum swelling and even degenerated. Others showed ruptured endothelial wall. Pericytes exhibited a cytoplasm which varied from normal to a proliferative one. The mononuclear cell infiltrate consisted of macrophages and neutrophils. Most of observed alterations have been described in muscle disorders with an autoimmune component.

[Equine Infectious Anemia (EIA)]. / Equine Infektiöse Anämie (EIA).

Equine Infectious Anemia (EIA) is a reportable, eradicable epizootic disease caused by the equine lentivirus of the retrovirus family which affects equids only and occurs worldwide. The virus is transmitted by blood, mainly by sanguivorous insects. The main symptoms of the disease are pyrexia, apathy, loss of body condition and weight, anemia, edema and petechia. However, infected horses can also be inapparent carriers without any overt signs. The disease is diagnosed by serological tests like the Coggins test and ELISA tests. Presently, Switzerland is offi cially free from EIA. However, Switzerland is permanently at risk of introducing the virus as cases of EIA have recently been reported in different European countries.

Leukoencephalitis associated with selective viral replication in the brain of a pony with experimental chronic equine infectious anemia virus infection.

Neurologic disease occurs sporadically in horses infected with the equine infectious anemia virus (EIAV). This report describes a case of clinically severe neurologic disease in a pony experimentally infected with EIAV. This pony did not have fever or anemia, which are the characteristic clinical signs of disease. The histopathologic changes were characterized as lymphohistiocytic periventricular leukoencephalitis. Polymerase chain reaction and in situ hybridization data showed that the brain lesions were directly associated with viral replication and that high-level viral replication occurred selectively within the lesion and not in other tissues. These findings suggest that EIAV-associated neurologic disease is the direct result of viral replication.

Platelets from thrombocytopenic ponies acutely infected with equine infectious anemia virus are activated in vivo and hypofunctional.

Thrombocytopenia is a consistent finding and one of the earliest hematological abnormalities in horses acutely infected with equine infectious anemia virus (EIAV), a lentivirus closely related to human immunodeficiency virus. Multifactorial mechanisms, including immune-mediated platelet destruction and impaired platelet production, are implicated in the pathogenesis of EIAV-associated thrombocytopenia. This study was undertaken to investigate whether regenerative thrombopoiesis and platelet destruction occurred in ponies acutely infected with EIAV. Circulating large, immature platelets were increased in ponies acutely infected with EIAV late in the infection when platelet count was at a nadir. Morphometric analysis of bone marrow from acutely infected ponies revealed significant increased in megakaryocyte area and megakaryocyte nuclear area. A trend toward increased numbers of megakaryocytes was also observed. Platelets from acutely infected ponies had increased surface-bound fibrinogen and ultrastructural changes consistent with in vivo platelet activation. Platelets also had hypofunctional aggregation responses to three agonists in vitro. We conclude that thrombocytopenia in ponies acutely infected with EIAV is regenerative and suggest that bone marrow platelet production is not severely compromised in these ponies. Our findings reveal that in vivo platelet activation occurs in ponies acutely infected with EIAV, and as a result platelets are hypofunctional in vitro. Activation of platelets in vivo may cause platelet degranulation or formation of platelet aggregates, which would result in removal of these damages platelets from circulation. This may represent a form of nonimmune-mediated platelet destruction in ponies acutely infected with EIAV.

Infection of bone marrow macrophages by equine infectious anemia virus.

OBJECTIVE: To characterize infection of bone marrow-derived macrophages (BMDM) with equine infectious anemia virus (EIAV) by determining virus production, effects on viability, and induction of cytokines. SAMPLE POPULATION: BMDM obtained from bone marrow of 6 clinically normal adult horses. PROCEDURE: BMDM were infected with EIAV at a multiplicity of infection of 8. Cell viability, percentage of cells with detectable viral protein, reverse transcriptase activity, and concentrations of infective virus (focus-forming units/ml), interleukin 6, and tumor necrosis factor-alpha were measured in culture supernatant samples obtained at various days after infection. RESULTS: Cell viability was decreased on day 4 and was maximally decreased on day 8. The number of cells with detectable viral protein and supernatant reverse transcriptase activity increased significantly on day 4 and increased until day 6. Virus concentration (focus-forming units per milliliter) peaked on day 4 after infection and was constant thereafter. Infection with EIAV caused significant induction of interleukin 6 production by BMDM. The maximal difference was seen on day 4 after infection. Control and infected BMDM produced only negligible amounts of tumor necrosis factor-alpha. CONCLUSIONS: BMDM are useful, as a cell population, to study the effects of infection with EIAV, including cell death and induction of interleukin 6 but not tumor necrosis factor-alpha production.

Flow cytometric method for detecting thiazole orange-positive (reticulated) platelets in thrombocytopenic horses.

OBJECTIVE: To evaluate a method for detecting thiazole orange-positive (TO+, reticulated) platelets in equine blood, using flow cytometry. ANIMALS: 16 healthy, equine infectious anemia virus (EIAV)-negative horses and ponies; 9 thrombocytopenic, EIAV-positive horses and ponies; and 2 thrombocytopenic, EIAV-negative horses. PROCEDURE: Blood from healthy and thrombocytopenic horses was collected by jugular venipuncture. Appropriate sample requirement and incubation time for the assay were evaluated, using blood anticoagulated with EDTA or sodium citrate, or platelet-rich plasma in sodium citrate. The sample of blood or platelet-rich plasma was incubated with thiazole orange, and flow cytometric analysis was performed. Percentage of circulating TO+ platelets was determined from fluorescence (FL-1) logarithmic histograms. RESULTS: Healthy ponies (n = 9) had 1.28 to 2.83% (mean +/- SD, 2.03 +/- 0.50%) and horses (n = 7) had 0.9 to 3.44% (2.12 +/- 1.14%) TO+ platelets in circulation. Thrombocytopenic ponies (n = 7) had 11.14 to 48.41% (26.51 +/- 11.99%) and thrombocytopenic horses (n = 4) had 2.33 to 8.52% (6.19 +/- 2.68%) TO+ platelets in circulation. Mean platelet counts for the thrombocytopenic ponies and horses were 24,400 +/- 20,500 and 39,300 +/- 13,500 platelets/microliters, respectively (reference range, 94,000 to 232,000 platelets/ microliters). CONCLUSION: Thiazole orange-positive platelets can be detected in equine blood and percentages of TO+ platelets are increased in thrombocytopenic horses. CLINICAL RELEVANCE: Enumeration of TO+ platelets may prove to be a helpful noninvasive clinical measurement of bone marrow platelet production and aid in the assessment of platelet kinetics in thrombocytopenic horses.

Suppression of megakaryocyte colony growth by plasma from foals infected with equine infectious anemia virus.

Foals infected with equine infectious anemia virus become thrombocytopenic 7 to 20 days after virus inoculation, and within a few days following the onset of detectable viremia. The thrombocytopenia is associated with suppression of platelet production. Possible mediators of suppression of thrombopoiesis include tumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta (TGF-beta), cytokines that are released during inflammation. To assess effects of plasma or serum from infected foals on megakaryocyte (MK) growth and maturation in vitro, equine low-density bone marrow cells were cultured for clonogenic and ploidy assays. Neutralizing antibodies to TNF-alpha and TGF-beta were added to cultures to determine the contribution of these cytokines to suppression of thrombopoiesis. Plasma from the immediately pre-thrombocytopenia (Pre-Tp) period significantly reduced MK colony numbers. This suppression was partially reversed upon antibody neutralization of plasma TNF-alpha, TGF-beta, or both. There were no differences in ploidy distribution of MK grown in the presence of preinfection serum compared with those grown in the presence of Pre-Tp serum. These results indicate that TNF-alpha and TGF-beta may contribute to suppression of MK proliferation and represent likely factors in the pathogenesis of thrombocytopenia.