ABSTRACT
Contagious agalactia is a disease caused by Mycoplasma agalactiae that leads to a reduction or complete stop of milk production. Caprine arthritis encephalitis (CAE) is an infectious disease caused by a lentivirus of the Retroviridae family, member of the small ruminant lentivirus (SRLV) group. Although these diseases are caused by distinct pathogens, the clinical presentation is similar. Hence, this study aimed to perform a serological investigation, as well as to assess correlation between both diseases and risk factors associated in two mesoregions of Rio Grande do Norte, Brazil. Enzyme-linked immunosorbent assay (ELISA) was used for contagious agalactia and western blot for CAE. A total of 538 serum samples were used in this study that were collected from goats and sorted from a blood bank of the Brazilian Agricultural Research Corporation. Seroprevalence of M. agalactiae in flocks from Rio Grande do Norte was 7.8% (42/538). In both regions that were investigated, 25.9% (14/54) of farms had positive animals. CAE results revealed that 3.9% (21/538) of animals and 42.6% (23/54) of farms had this disease. Concerning risk factors, only sex and animal category presented significant relevance (P < 0.05) for contagious agalactia, in which females presented higher frequency of seropositive individuals (10.1%; 39/387). In the animal category, 4.3% (14/326) and 11.1% (36/323) of female breeders were positive for CAE and contagious agalactia, respectively, and significance was identified only in the latter (P < 0.05). In conclusion, there was no correlation between the investigated diseases, considering that no animal demonstrated antibodies for both pathogens.
Subject(s)
Arthritis-Encephalitis Virus, Caprine/isolation & purification , Goat Diseases/epidemiology , Lentivirus Infections/veterinary , Mycoplasma Infections/veterinary , Mycoplasma agalactiae/isolation & purification , Animals , Brazil/epidemiology , Coinfection , Enzyme-Linked Immunosorbent Assay/veterinary , Female , Goat Diseases/microbiology , Goats , Lentivirus Infections/complications , Lentivirus Infections/epidemiology , Male , Mycoplasma Infections/complications , Mycoplasma Infections/epidemiology , Risk Factors , Seroepidemiologic StudiesABSTRACT
Tooth resorption (TR) is one of the most common dental diseases in cats. Determination of risk factors has not yet been fully assessed and, to the best knowledge of the authors, this disease has never been studied in Portuguese cats. The objective of this case-control study was to determine type and distribution of TR lesions, evaluate risk factors, and establish relationships between variables in this disease. The study included data from 71 cats admitted for general anesthesia for various reasons. The cats were randomly selected. The inclusion criteria were availability of clinical history and owner permission. Cats with known oral disease were not excluded from the study. All cats received ultrasonic scaling and polishing of the teeth, a thorough oral examination, and full-mouth radiographs. A strong statistical relation was found between age and TR. The age group of 10 to 15-years showed an increased risk of 6.56 times for TR occurrence compared with the group 0 to 4-years of age. Presence of gingivitis in all index levels was related to an increased risk for TR. No relation was found between age or gingivitis index and lesion type. Mandibular third premolar and molar teeth were most commonly affected by TR, especially for type 1 lesions. Canine teeth were statistically more likely to have type 2 lesions. The trend for the canine teeth to be more affected with type 2 lesions needs further verification.
Subject(s)
Cat Diseases/etiology , Tooth Resorption/veterinary , Age Factors , Animals , Bicuspid/pathology , Case-Control Studies , Cats , Cuspid/pathology , Dental Prophylaxis/veterinary , Dental Scaling/veterinary , Female , Gingival Hemorrhage/complications , Gingival Hemorrhage/veterinary , Gingival Hypertrophy/complications , Gingival Hypertrophy/veterinary , Gingivitis/classification , Gingivitis/complications , Gingivitis/veterinary , Immunodeficiency Virus, Feline/isolation & purification , Lentivirus Infections/complications , Lentivirus Infections/veterinary , Lentiviruses, Feline/isolation & purification , Male , Molar/pathology , Portugal , Radiography, Dental/veterinary , Risk Assessment , Tooth Resorption/etiologyABSTRACT
Bovine tuberculosis (BTB), caused by Mycobacterium bovis, is a disease that was introduced relatively recently into the Kruger National Park (KNP) lion population. Feline immunodeficiency virus (FIV(ple)) is thought to have been endemic in lions for a much longer time. In humans, co-infection between Mycobacterium tuberculosis and human immunodeficiency virus increases disease burden. If BTB were to reach high levels of prevalence in lions, and if similar worsening effects would exist between FIV(ple) and BTB as for their human equivalents, this could pose a lion conservation problem. We collected data on lions in KNP from 1993 to 2008 for spatio-temporal analysis of both FIV(ple) and BTB, and to assess whether a similar relationship between the two diseases exists in lions. We found that BTB prevalence in the south was higher than in the north (72 versus 19% over the total study period) and increased over time in the northern part of the KNP (0-41%). No significant spatio-temporal differences were seen for FIV(ple) in the study period, in agreement with the presumed endemic state of the infection. Both infections affected haematology and blood chemistry values, FIV(ple) in a more pronounced way than BTB. The effect of co-infection on these values, however, was always less than additive. Though a large proportion (31%) of the lions was co-infected with FIV(ple) and M. bovis, there was no evidence for a synergistic relation as in their human counterparts. Whether this results from different immunopathogeneses remains to be determined.
Subject(s)
Lentivirus Infections/veterinary , Lions/microbiology , Lions/virology , Mycobacterium bovis/isolation & purification , Tuberculosis/veterinary , Africa , Animals , Female , Lentivirus Infections/complications , Lentivirus Infections/epidemiology , Linear Models , Male , Models, Theoretical , Sex Factors , Time Factors , Tuberculosis/complications , Tuberculosis/epidemiologyABSTRACT
Prions are misfolded proteins that are infectious and naturally transmitted, causing a fatal neurological disease in humans and animals. Prion shedding routes have been shown to be modified by inflammation in excretory organs, such as the kidney. Here, we show that sheep with scrapie and lentiviral mastitis secrete prions into the milk and infect nearly 90% of naïve suckling lambs. Thus, lentiviruses may enhance prion transmission, conceivably sustaining prion infections in flocks for generations. This study also indicates a risk of prion spread to sheep and potentially to other animals through dietary exposure to pooled sheep milk or milk products.
Subject(s)
Lentivirus Infections/veterinary , Mastitis/complications , Milk/chemistry , Prions/isolation & purification , Scrapie/complications , Scrapie/transmission , Sheep Diseases/virology , Animals , Disease Models, Animal , Female , Histocytochemistry , Immunohistochemistry , Infectious Disease Transmission, Vertical , Lentivirus Infections/complications , Mammary Glands, Animal/pathology , Mastitis/virology , Microscopy , Sheep , Visna-maedi virus/isolation & purificationABSTRACT
BACKGROUND: Age-related dementia has been documented in domestic cats; however, its interaction with naturally occurring feline immunodeficiency virus (FIV) infection has been investigated minimally. METHODS: Visuospatial working memory (VSWM) and problem-solving (PS) ability were evaluated in FIV-infected (n = 37) and control cats (n = 39) using two cognitive tasks tested serially, which assessed the ability of cats to remember the location of a baited container after a set delay, then evaluated the capability of the cats to manipulate the container to obtain the food within a time limit. Cats were categorized using 7 years of age as a cut-off to determine age-related differences. The relationship between cognitive performance and FIV viral load was investigated using real-time PCR cycle threshold (Ct ) values. RESULTS: Age significantly affected VSWM and PS ability. Younger cats had better VSWM performance and PS ability compared to older cats with the same FIV status. There was no difference between younger FIV-positive and negative cats in either part of the task. While older FIV-positive cats had significantly worse VSWM than older FIV-negative cats, no differences were found in PS ability. Additionally, Ct values predicted VSWM but not PS ability. CONCLUSION: Age-related cognitive impairments and FIV infection appear synergetic, causing greater cognitive deficits in older FIV-infected cats.
Subject(s)
Cat Diseases , Cognitive Dysfunction , Feline Acquired Immunodeficiency Syndrome , Immunodeficiency Virus, Feline , Lentivirus Infections , Animals , Cats , Feline Acquired Immunodeficiency Syndrome/complications , Lentivirus Infections/complications , Lentivirus Infections/veterinary , Real-Time Polymerase Chain Reaction/veterinaryABSTRACT
Caprine arthritis encephalitis virus (CAEV) is a monocyte/macrophage-tropic lentivirus that primarily infects goats resulting in a well-recognized set of chronic inflammatory syndromes focused on the joint synovium, tissues of the central nervous system, pulmonary interstitium and mammary gland. Clinically affected animals generally manifest with one or more of these classic CAEV-associated tissue lesions; however, CAEV-associated renal inflammation in goats has not been reported in the peer-reviewed literature. Here we describe six goats with chronic, multisystemic CAEV infections in conjunction with CAEV-associated renal lesions. One of the animals had CAEV antigen-associated thrombotic arteritis resulting in infarction of both the kidney and heart. These goats had microscopic evidence of inflammatory renal injury (interstitial nephritis) with detectable renal immunolabeling for CAEV antigen in three of six animals and amplifiable proviral sequences consistent with CAEV in all six animals. Cardiac lesions (vascular, myocardial or endocardial) were also identified in four of six animals. Within the viral promoter (U3) region, known transcription factor binding sites (TFBSs) were generally conserved, although one viral isolate had a duplication of the U3 A region encoding a second gamma-activated site (GAS). Despite the TFBS conservation, the isolates demonstrated a degree of phylogenetic diversity. At present, the clinical consequence of CAEV-associated renal injury is not clear.
Subject(s)
Arthritis-Encephalitis Virus, Caprine/pathogenicity , Kidney/pathology , Kidney/virology , Lentivirus Infections/complications , Lentivirus Infections/veterinary , Nephritis, Interstitial/veterinary , Nephritis, Interstitial/virology , Animals , Arthritis-Encephalitis Virus, Caprine/classification , Arthritis-Encephalitis Virus, Caprine/genetics , Goat Diseases/blood , Goat Diseases/virology , Goats/virology , Inflammation/virology , Kidney/immunology , Lentivirus Infections/blood , Phylogeny , Promoter Regions, Genetic , Proviruses/geneticsABSTRACT
Domestic cats serve as the reservoir hosts of Bartonella henselae and may develop mild clinical symptoms or none after experimental infection. In humans, B. henselae infection can result in self-limiting cat scratch disease. However, immunocompromised patients may suffer from more-severe courses of infection or may even develop the potentially lethal disease bacillary angiomatosis. It was reasoned that cats with immunocompromising viral infections may react similarly to B. henselae infection. The aim of our study was to investigate the influence of the most important viruses known to cause immunosuppression in cats-Feline leukemia virus (FeLV), Feline immunodeficiency virus (FIV), and Feline panleukopenia virus (FPV)-on natural B. henselae infection in cats. Accordingly, 142 cats from animal shelters were necropsied and tested for B. henselae and concurrent infections with FeLV, FIV, or FPV by PCR and immunohistochemistry. A significant association was found between B. henselae and FeLV infections (P = 0.00028), but not between B. henselae and FIV (P = 1.0) or FPV (P = 0.756) infection, age (P = 0.392), or gender (P = 0.126). The results suggest that susceptibility to B. henselae infection is higher in cats with concurrent FeLV infections, regardless of whether the infection is latent or progressive. Histopathology and immunohistochemistry for B. henselae failed to identify lesions that could be attributed specifically to B. henselae infection. We conclude that the course of natural B. henselae infection in cats does not seem to be influenced by immunosuppressive viral infections in general but that latent FeLV infection may predispose cats to B. henselae infection or persistence.
Subject(s)
Bartonella Infections/veterinary , Bartonella henselae/isolation & purification , Cat Diseases/virology , Leukemia Virus, Feline/isolation & purification , Retroviridae Infections/veterinary , Tumor Virus Infections/veterinary , Animals , Bartonella Infections/epidemiology , Bartonella Infections/microbiology , Cats , Comorbidity , Feline Panleukopenia/complications , Feline Panleukopenia/virology , Feline Panleukopenia Virus/isolation & purification , Female , Immunocompromised Host , Immunodeficiency Virus, Feline/isolation & purification , Lentivirus Infections/complications , Lentivirus Infections/veterinary , Lentivirus Infections/virology , Male , Prevalence , Retroviridae Infections/complications , Retroviridae Infections/virology , Tumor Virus Infections/complications , Tumor Virus Infections/virologyABSTRACT
OBJECTIVE: To investigate the association between naturally occurring chronic kidney disease (CKD) and FIV infection status in cats in Australia. DESIGN: Case-control study. ANIMALS: 73 cats with CKD and 69 cats without historical, physical, or clinicopathologic evidence of CKD. PROCEDURES: Cats were tested for serum antibodies against FIV glycoprotein 40 (gp40) by use of an immunomigration assay. Information regarding age, breed (purebred or domestic), and sex was obtained from medical records. Analysis was performed on data from cats stratified into 2 age categories (< 11 years old and >or= 11 years old). Univariable and then multivariable analyses were performed to investigate the relationship between CKD and the study variable (FIV infection), the latter analysis accounting for breed (purebred or domestic), sex, and veterinary hospital of origin. RESULTS: Results of multivariable analysis revealed that younger cats with CKD (< 11 years old) were significantly more likely to have positive test results for serum antibodies against FIV gp40 than were cats without CKD. No significant associations were found between CKD and FIV infection, breed, sex, or hospital of origin among older (>or= 11 years old) cats in the multivariable analysis. CONCLUSIONS AND CLINICAL RELEVANCE: Among cats < 11 years of age, those with CKD were significantly more likely to have positive test results for serum antibodies against FIV gp40 than were cats without CKD. It cannot be definitively established from results of this study whether infection with FIV preceded the development of CKD, and the role, if any, of FIV in the establishment or progression of CKD remains to be determined.
Subject(s)
Cat Diseases/virology , Immunodeficiency Virus, Feline , Kidney Failure, Chronic/veterinary , Lentivirus Infections/veterinary , Animals , Case-Control Studies , Cats , Female , Kidney Failure, Chronic/complications , Lentivirus Infections/complications , Male , Multivariate AnalysisABSTRACT
A longitudinal study was conducted in a single dairy goat herd to investigate the relationship between subclinical small ruminant lentivirus (SRLV) infection in does and litter size (LS) or birth body weight of kids (BW). Each year kids born to seropositive and seronegative does were weighed before the first consumption of colostrum. LS and BW of each kid were recorded. BW was significantly negatively linked to LS (p = 0.006) - singletons weighed (mean ± SD) 4.20 ± 0.67 kg, twins - 3.75 ± 0.62 kg, and triplets and quadruplets - 3.38 ± 0.47 kg. Male kids were significantly heavier than female kids in twin litters (3.97 ± 0.53 kg vs. 3.52 ± 0.60 kg; p < 0.001) and triplet or quadruplet litters (3.62 ± 0.40 kg vs. 3.17 ± 0.43 kg; p < 0.001). However, BW of male and female kids from singleton litters did not differ (4.31 ± 0.71 kg vs. 4.07 ± 0.65 kg; p = 0.154). Then, two mixed models were developed to assess the relationship between LS (mixed Poisson log linear regression model) or BW (mixed linear model) and SRLV infection in the doe, controlling for potential confounders such as the effect of an individual doe, year in which the parturition took place, parity and kid's sex. Neither LS nor BW proved to be significantly associated with SRLV infection (p = 0.788 and p = 0.214, respectively). On this basis it was concluded that LS and BW were not affected by the subclinical SRLV infection of a doe.
Subject(s)
Goat Diseases/virology , Lentivirus Infections/veterinary , Litter Size , Pregnancy Complications, Infectious/veterinary , Animals , Asymptomatic Infections , Birth Weight , Female , Goats/physiology , Goats/virology , Lentivirus Infections/complications , Lentiviruses, Ovine-Caprine , Male , Parity , PregnancyABSTRACT
Infection with small ruminant lentiviruses (SRLV) causes a variety of chronic inflammatory conditions that limit production. Mycobacterium avium subsp. paratuberculosis (MAP) is also a major production-limiting disease of sheep and goats, which causes severe inflammation of the small intestine. Previous studies have indicated that both SRLV and MAP are widespread in small ruminants in Ontario. This study estimated the prevalence of SRLV and MAP co-infection. Serum samples that were previously tested for MAP infection were re-tested for SRLV. The apparent prevalence of co-infection was low, with 3.4% [95% confidence interval (CI): 1.9 to 5.9] and 14.3% (95% CI: 11.6 to 17.5) of sheep and goats respectively, positive for both infections. However, co-infection is widespread with 36.8% (95% CI: 19.1 to 59.1) and 71.4% (95% CI: 52.8 to 84.9) of sheep and goat farms with 1 or more co-infected animals. A significant association was found between SRLV seropositivity and MAP fecal culture (P = 0.021), suggesting that co-infected goats may be more likely to shed MAP in their feces.
L'infection par lentivirus des petits ruminants (SRLV) provoque une variété d'états inflammatoires chroniques qui limitent la production. Mycobacterium avium subsp. paratuberculose (MAP) est aussi une maladie limitant la production majeure de moutons et de chèvres, ce qui provoque une inflammation grave de l'intestin grêle. Des études antérieures ont indiqué que les deux infections de SRLV et MAP sont très répandues dans l'Ontario petits ruminants. Cette étude a été réalisée pour estimer la prévalence de SRLV et MAP co-infection. Des échantillons de sérum qui avaient été préalablement testés pour l'infection de MAP ont été utilisés pour détecter des anticorps spécifiques SLRV. La prévalence de la co-infection était faible, avec 3,4 % intervalle de confiance (95% IC : 1,95,9) et 14,3 % (95% IC : 11,617,5) des ovins et caprins, respectivement, positive pour les deux infections. Cependant la co-infection est très répandue avec 36,8 % (95% IC : 19,159,1) et 71,4 % (95% IC : 52,884,9) des élevages ovins et caprins avec un ou plusieurs animaux co-infecté. Une association significative a été trouvée entre SRLV et séropositivité MAP culture fécale (P = 0,021), ce qui suggère que les chèvres co-infectés peuvent être plus susceptibles de jeter le MAP dans leurs excréments.(Traduit par les auteurs).
Subject(s)
Goat Diseases/epidemiology , Lentivirus Infections/veterinary , Lentiviruses, Ovine-Caprine/isolation & purification , Mycobacterium avium subsp. paratuberculosis/isolation & purification , Paratuberculosis/complications , Sheep Diseases/epidemiology , Animals , Cross-Sectional Studies , Goat Diseases/microbiology , Goat Diseases/virology , Goats , Lentivirus Infections/complications , Lentivirus Infections/epidemiology , Lentivirus Infections/virology , Ontario/epidemiology , Paratuberculosis/diagnosis , Paratuberculosis/epidemiology , Sheep , Sheep Diseases/microbiology , Sheep Diseases/virologyABSTRACT
Infection with immunosuppressive lentiviruses is associated with increased cancer risk,but most studies have implicated indirect mechanisms as the tumor cells generally lack integrated viral sequences. An exception wasfound in a B-cell lymphoma (Q254) where the tumor cells contained a single integrated feline immunodeficiency virus genome. Additional analysis now indicates that feline immunodeficiency virus integration in lymphoma Q254 resulted in promoter insertion and truncation of a conserved gene on feline chromosome B3, whereas the unaffected allele of the gene appeared to be transcriptionally down-regulated. The orthologous human gene (FLJ12973), is expressed ubiquitously and encodes a WD-repeat protein with structural similarity to DDB2, the small subunit of the xeroderma pigmentosum XP-E complex. Moreover, the gene is located within a region of frequent tumor-specific deletions on chromosome 15q15. These observations demonstrate the direct mutagenic potential of the lentiviruses and identify a new candidate tumor suppressor gene.
Subject(s)
Chromosomes, Human, Pair 15/genetics , Genes, Tumor Suppressor , Immunodeficiency Virus, Feline/genetics , Lymphoma, B-Cell/virology , Amino Acid Sequence , Animals , Base Sequence , Cats , Genome, Viral , Humans , Lentivirus Infections/complications , Lentivirus Infections/genetics , Lentivirus Infections/veterinary , Lentivirus Infections/virology , Lymphoma, B-Cell/genetics , Lymphoma, B-Cell/veterinary , Molecular Sequence Data , Sequence Alignment , Transcriptional Activation , Virus IntegrationABSTRACT
CASE DESCRIPTION A 17-year-old FIV-positive cat was evaluated because of weight loss during the preceding few months. The cat had a weight loss of 0.5 kg (1.1 lb) during the last month. Because of its FIV-positive status, the cat was confined indoors. CLINICAL FINDINGS A large nonpruritic area of alopecia with hyperpigmentation and comedones was present on the right lateral aspect of the neck. The chin had diffuse alopecia and comedones. Mild alopecia was present on the dorsal aspect of the muzzle. Trichography and microscopic examination of acetate tape imprint preparations and skin scrapings revealed a very morphologically heterogeneous population of Demodex mites. Micrometry of adult mites revealed a broad range of body lengths (92.68 to 245.94 µm), which suggested that as many as 3 Demodex spp might be present in the skin lesions of this cat. TREATMENT AND OUTCOME Owing to its concurrent disease, no treatment was initiated for the demodicosis, and the cat died spontaneously 14 days after the evaluation. Sequence analysis of the 16S rRNA gene of collected mites was performed. Analysis revealed that the 16S rRNA gene sequence of collected mites appeared 100% identical to the Demodex cati 16S rRNA gene sequence deposited in GenBank (JX193759). A similarity of 79.2% and 74.4% was found when the 16S rRNA gene sequence of collected mites was compared with that of Demodex gatoi (JX981921) and Demodex felis (KF052995), respectively. CLINICAL RELEVANCE Demodicosis in cats is often associated with underlying disease. In cats, FIV infection may lead to an altered immune response and induce species polymorphism of Demodex mites.
Subject(s)
Immunodeficiency Virus, Feline , Lentivirus Infections/veterinary , Mite Infestations/veterinary , Mites/classification , Animals , Cats , Lentivirus Infections/complications , Lentivirus Infections/virology , Male , Mite Infestations/complications , Mites/genetics , RNA, Ribosomal, 16S/geneticsABSTRACT
Leishmaniosis is a group of diseases caused by different species of Leishmania parasites in mammalian species. The aim of the present study was to investigate the presence of Leishmania spp. DNA in cats using real time polymerase chain reaction (RT-PCR) assays targeting internal transcribed spacer (ITS1) and heat-shock protein 70 gene (Hsp70) regions with Leishmania species-specific primers and probes. Blood samples were collected from 147 cats (73 female; 74 male) in the endemic regions for zoonotic visceral leishmaniasis in the western provinces of Turkey and analyzed using two RT-PCR assays. Additionally, Hsp70 RT-PCR products were sequenced. ELISA assays for feline immunodeficiency virus (FIV) and feline leukemia virus (FeLV) were also carried out for 145 of the 147 samples. Overall, 13/147 (8.84%) cats were positive for Leishmania by RT-PCR (4 L. major and 9 L. tropica). FIV and FeLV antibody and/or antigen was detected in 4 and 5 cats among Leishmania DNA positives, respectively. To the best of our knowledge, this study is the first to investigate and report the presence of L. major and L. tropica infections in a large group of domestic cats in Turkey. The results obtained indicate that species identification of Leishmania is essential for epidemiological understanding and that clinical signs alone are not indicative for leishmaniosis in cats, as it is in dogs. This study suggests that extensive research should be carried out in cat populations in order to fully understand the role of cats in the epidemiology of the disease.
Subject(s)
Cat Diseases/parasitology , Leishmania major , Leishmania tropica , Leishmaniasis, Cutaneous/veterinary , Animals , Antibodies, Viral/blood , Cat Diseases/blood , Cat Diseases/epidemiology , Cat Diseases/virology , Cats , Coinfection , Female , Immunodeficiency Virus, Feline/isolation & purification , Leishmaniasis, Cutaneous/complications , Leishmaniasis, Cutaneous/epidemiology , Leishmaniasis, Cutaneous/parasitology , Lentivirus Infections/complications , Lentivirus Infections/epidemiology , Lentivirus Infections/veterinary , Leukemia Virus, Feline/isolation & purification , Male , Retroviridae Infections/complications , Retroviridae Infections/epidemiology , Retroviridae Infections/veterinary , Tumor Virus Infections/complications , Tumor Virus Infections/epidemiology , Tumor Virus Infections/veterinary , Turkey/epidemiologyABSTRACT
The effect of experimental primary-stage feline immunodeficiency virus (FIV) infection on feline calicivirus (FCV) vaccination and challenge in cats was studied. Clinical signs of acute FCV disease were more widespread in the cats which were infected with FIV than in those which were not. FIV infection also prolonged shedding of FCV, with more of the FIV-infected cats becoming chronic carriers. Although vaccination induced protection against acute FCV disease, this was to a lesser degree in FIV-infected cats. Vaccination by itself also appeared to enhance long-term virus shedding. There was evidence of an impaired anamnestic FCV-neutralizing antibody response in FIV-infected cats following FCV challenge.
Subject(s)
Caliciviridae/immunology , Cat Diseases/immunology , Immunodeficiency Virus, Feline , Lentivirus Infections/veterinary , Picornaviridae Infections/veterinary , Animals , Cats , Chronic Disease , Lentivirus Infections/complications , Lentivirus Infections/immunology , Picornaviridae Infections/complications , Picornaviridae Infections/immunology , Specific Pathogen-Free Organisms , VaccinationABSTRACT
This report describes the gross, histopathological, immunocytochemical and electron microscopic findings in a cat with systemic cryptococcosis and feline immunodeficiency virus (FIV) infection. Lymphadenopathy and cloudiness of leptomeninges were the major gross findings. Numerous cryptococcal yeasts were found in lymph nodes, brain, and lung, and were less common in the kidney and the eye. The inflammatory reaction varied in intensity and cell type (mononuclear through granulomatous) depending on the organ involved. Yeasts were mainly within phagocytes as revealed by electron microscopy. Some inflammatory cells were immunocytochemically-stained with anti-CD3 antibodies.
Subject(s)
Cryptococcosis/pathology , Immunodeficiency Virus, Feline , Lentivirus Infections/pathology , Animals , CD3 Complex/immunology , Cats , Cryptococcosis/complications , Cryptococcosis/microbiology , Dogs , Immunohistochemistry , Lentivirus Infections/complications , Lymph Nodes/pathology , Male , Meninges/pathology , Microscopy, Electron , Phagocytes/microbiology , Phagocytes/ultrastructureABSTRACT
Clinical, serological, and pathological abnormalities observed in Holstein cows naturally infected with bovine lentivirus 1 bovine immunodeficiency virus (BIV) and other infections were progressive and most commonly associated with weight loss, lymphoid system deficiency, and behavioral changes. Clinical evidence of meningoencephalitis was dullness, stupor, and occasional head or nose pressing postures. The polymerase chain reactions associated the BIV provirus with the lesions in the central nervous system and lymphoid tissues. Multiple concurrent infections developed in retrovirally infected cows undergoing normal stresses associated with parturition and lactation. A major functional correlate of the lymphoreticular alterations was the development of multiple secondary infections which failed to resolve after appropriate antibacterial therapy. The chronic disease syndrome in dairy cows associated with BIV may be useful as a model system for investigation of the pathogenesis of the nervous system lesions and lymphoid organ changes that occur in humans with lentiviral infection.
Subject(s)
Lentivirus Infections/veterinary , Lentiviruses, Bovine/isolation & purification , Animals , Antibodies, Viral/blood , Bovine Virus Diarrhea-Mucosal Disease/complications , Bovine Virus Diarrhea-Mucosal Disease/pathology , Brain/pathology , Brain/virology , Cattle , DNA, Viral/chemistry , DNA, Viral/genetics , Diarrhea Viruses, Bovine Viral/isolation & purification , Female , Histocytochemistry/veterinary , Lentivirus Infections/blood , Lentivirus Infections/complications , Lentivirus Infections/pathology , Lentiviruses, Bovine/genetics , Lymphoid Tissue/pathology , Lymphoid Tissue/virology , Polymerase Chain Reaction/veterinaryABSTRACT
Encephalitis, lymphoid tissue depletion and secondary infections occurred over a 5-yr-period in Holstein cows infected with bovine immunodeficiency virus (BIV). There were 59 cattle studied, the majority during 1991, when a severe environmental stress occurred, each with one or more primary causes of death, natural or by euthanasia, and most with several secondary diseases. The encephalitis was characterized by meningeal, perivascular and parenchymal infiltration with lymphocytes, occasional plasma cells and macrophages with perivascular edema in some cows. Affected areas included the cerebrum, cerebellum, and spinal cord with no particular distribution pattern recognized. The lymphoid depletion was primarily an absence of follicular development in nodes draining regions with secondary infections such as chronic mastitis and chronic suppurative pododermatitis. Paucity of lymphocytes in thymic-dependent regions of lymph nodes and the spleen suggested a primary depletion of T cells. Secondary infections were often multiple with each cow having several minor conditions, usually considered short-term and treatable. These included mastitis and pododermatitis, with many cows having non-responding abscesses, cellulitis and myositis attributed to injection site infections. A large number of the cattle had parturition difficulties such as dystocia, obturator paralysis, and metritis. Pulmonary, cardiovascular, and intestinal disease were recognized as both primary and secondary disease conditions. There was a high level of infection with bovine leukemia virus with 4 of the 59 cattle having lymphosarcoma. Under practical conditions, the infection with BIV has a different effect on the host than has been observed under experimental conditions. The presence of BIV combined with the stresses associated with parturition and a modern dairy production system were considered causal for the development of untreatable secondary diseases in immunocompromised cattle. The peak incidence in 1991 was attributed to increased environmental stress during renovation of the barn facility. During this time the cattle were kept on open pasture, exposed to an extremely wet winter, and spring weather conditions. The effect of co-infection with bovine leukemia virus, the influence of immunocompromise on the chronicity of mastitis, the relationship with laminitis and pododermatitis, and several questions related to viral transmission, complementarism with bovine leukemia virus, viral reactivation and immunoprophylaxis all remain as viable avenues for future investigations.
Subject(s)
Cattle Diseases/etiology , Encephalitis, Viral/veterinary , Immunodeficiency Virus, Bovine/pathogenicity , Lentivirus Infections/veterinary , Lymphoid Tissue/pathology , Animals , Base Sequence , Cattle , Cattle Diseases/pathology , DNA Primers/genetics , DNA, Viral/genetics , DNA, Viral/isolation & purification , Encephalitis, Viral/complications , Enzootic Bovine Leukosis/complications , Female , Immunodeficiency Virus, Bovine/genetics , Immunodeficiency Virus, Bovine/isolation & purification , Lentivirus Infections/complications , Lentivirus Infections/etiology , Mastitis, Bovine/complications , Molecular Sequence Data , Opportunistic Infections/complications , Opportunistic Infections/veterinaryABSTRACT
Immune responses were examined in cattle between 3-5 years after experimental inoculation with bovine immunodeficiency virus (BIG) and/or bovine leukemia virus (BLV). Lymphocyte proliferative responses to Con A or to allogeneic lymphocytes with foreign major histocompatibility complex molecules (allo MHC) were determined by 3H-thymidine incorporation assays. Antigen-specific antibody and lymphocyte proliferative responses were measured following vaccination with tetanus toxoid (TT) and bovine herpes virus-1 (BHV-1). Lymphocytes from BIV-infected cattle had significantly (p<0.05) reduced proliferative responses to Con A, but responses to allo-MHC and TT did not differ from those of uninfected controls. BIV infection also had little effect on TT-specific antibody responses in vivo. In contrast, BLV-infected cattle had significantly increased secondary antibody responses to vaccination with TT, as well as enhancement of antibody responses to BHV-1. Co-infection with BIV did not alter the BLV effect, suggesting a lack of significant interaction between the two viruses in vivo. Numbers of circulating mononuclear cells were also higher in BLV-infected cattle, which was attributable to increases in both T and B cell numbers. Unstimulated lymphocytes from BLV-infected cattle had significantly increased spontaneous uptake of 3H-thymidine in vitro. When differences in counts per minute were analyzed, lymphocytes from BLV-infected cattle had slightly increased proliferative responses to Con A, but no consistent alternations in responsiveness to allo-MHC, TT, or BHV-1. The observed increase in antibody responses to non-BLV antigens suggests that at least in clinically asymptomatic cattle, BLV infection may cause a non-specific B cell activation.
Subject(s)
Antibodies, Viral/analysis , Enzootic Bovine Leukosis/immunology , Immunodeficiency Virus, Bovine/immunology , Lentivirus Infections/veterinary , Leukemia Virus, Bovine/immunology , Lymphocyte Activation , Animals , Antibody Formation , Blood Cell Count/veterinary , Cattle , Cattle Diseases/immunology , Enzootic Bovine Leukosis/complications , Enzyme-Linked Immunosorbent Assay/veterinary , Herpesvirus 1, Bovine/immunology , Immunity, Cellular , Lentivirus Infections/complications , Lentivirus Infections/immunology , Lymphocyte Culture Test, Mixed/veterinary , Male , Tetanus Toxoid/immunology , Vaccination/veterinaryABSTRACT
Increased susceptibility to intracellular pathogens in HIV-infected individuals and FIV-infected cats is attributed to a defective T-helper 1 (Th1) immune response. However, little is known about specific cytokine responses to secondary pathogens. To address this question, control and FIV-infected cats were challenged with Toxoplasma gondii, and lymph node cells analyzed for cytokine mRNA expression. Twenty-four weeks post-FIV infection, prior to T. gondii challenge, IL2 and IL12 mRNAs were depressed, whereas IL10 and IFNgamma mRNAs were increased in CD4+ and CD8+ subsets. Following T. gondii challenge, control cats showed increased expression of IL2, IFNgamma, IL10, IL12, and IL6 mRNAs. In contrast, IL2, IL6, IFNgamma, and IL12 mRNAs were suppressed in FIV-T. gondii co-infected cats, whereas IL10 remained at the high prechallenge levels. IFNgamma and IL10 mRNAs were produced by both CD4+ and CD8+ cells in FIV-T. gondii cats. Elevated IL10 may suppress a Th1 cytokine response to T. gondii challenge.
Subject(s)
Cat Diseases/immunology , Immunodeficiency Virus, Feline , Interleukins/genetics , Lentivirus Infections/veterinary , Toxoplasmosis, Animal/immunology , Animals , CD4-Positive T-Lymphocytes/immunology , CD8-Positive T-Lymphocytes/immunology , Cat Diseases/genetics , Cats , Gene Expression , Interleukin-10/genetics , Interleukin-12/genetics , Interleukin-2/genetics , Interleukin-6/genetics , Lentivirus Infections/complications , Lentivirus Infections/genetics , Lentivirus Infections/immunology , RNA, Messenger/genetics , RNA, Messenger/metabolism , T-Lymphocytes/immunology , Toxoplasmosis, Animal/complications , Toxoplasmosis, Animal/geneticsABSTRACT
Cats are important in the epidemiology of Toxoplasma gondii infection because they are the only hosts that can excrete the environmentally resistant oocysts. Antibodies to T. gondii were determined in serum samples from 220 domestic cats (Felis catus) from Barcelona, Spain, using the modified agglutination test (MAT). Antibodies to T. gondii were found in 99 (45%) of 220 cats, with MAT titers of 1:25 in 26, 1:50 in 57, and > or = 1:500 in 16 cats. Seropositivity (MAT 1:25 or more) was significantly higher in adult (> or = 1 yr old, 49.7% of 153) than in juvenile (< 1 yr old, 34.3% of 67) cats, in feral (51.9% of 131) than in domiciled (34.8% of 89) cats, and in cats living in a group (community) of more than 5 cats (50.7% of 142) than in cats living alone (28.0% of 50). These seropositive cats are likely to have already shed T. gondii oocysts in the environment around Barcelona.