Abstract Feline immunodeficiency virus (FIV) is an important infectious agent of domestic cats worldwide. It has been classified into the Lentivirus genus of the Retroviridae family, together with human immunodeficiency virus (HIV). Five FIV subtypes (A, B, C, D and E) have been described based on sequence variation of the V3-V5 region of the envelope (env) gene. There is considerable sequence diversity within and between subtypes, which has been a major obstacle in the development of a successful vaccine. However, an FIV vaccine that incorporates inactivated whole viruses from subtypes A and D is now commercially available. Although the vaccine has been shown to be efficacious in protecting against challenge with homologous and a heterologous (subtype B) subtypes, its effectiveness against other viral variants is unknown. Therefore, identifying the type and diversity of FIV strains in different regions is important to establish the potential efficacy of the vaccine in areas where vaccination is to be implemented. The proviral DNA sequence of the V3-V5 region of the env gene was determined for 102 FIV-infected cats from locations in Australia, New Zealand and South Africa. Subtype A was the predominant subtype in Australia and South Africa, although subtype B and C were also identified in each of these countries, respectively. Both subtypes A and C were also present in New Zealand. Of interest, there were some samples in New Zealand and South Africa that demonstrated subtype assignment discrepancies when different regions of the genome were analysed, suggesting co-infection and/or recombination. Cats infected with FIV exhibit varying degrees of immunological impairment. Currently, prognosis for an FIV-infected cat is based on clinical signs alone, which is a relatively subjective measure. In HIV-infected patients it is recognised that viral RNA load correlates with disease stage and prognosis. This PhD research tested whether viral RNA load may be a useful prognostic marker in FIV infection. A real-time PCR assay was developed to quantify plasma viral RNA load in 42 FIV-infected cats at three different clinical stages (1:healthy, 2:unwell without signs of immunodeficiency, 3:unwell with signs of immunodeficiency). In cats older than 5 years of age, log-transformed viral RNA loads were significantly higher in cats in category 3 compared to cats in category 1. There were no significant differences in the viral RNA load of older cats in category 2 compared to category 1. There were no cats younger than 5 years of age in category 3 and there was no significant difference in viral RNA load between young cats in categories 1 and 2. Of the 15 cats for which follow-up data was available, eight showed no change in clinical signs, and seven showed a worsening of clinical signs with six of these showing a progression of clinical category including death. One of the cats in category 2 that progressed clinically had one of the highest viral RNA loads of cats in that category. Three of four cats from category 3 that were followed had either died or been euthanised. Two of these cats had among the highest viral RNA loads in the whole study, while the remaining cat (for which the definitive cause of death was not confirmed) had a relatively low viral RNA load. In summary, measurement of viral RNA load was found to be a potentially useful clinical and prognostic marker but further work is required to better assess its usefulness to veterinarians. Serum acute phase proteins were investigated as possible candidate markers of FIV disease with the aim of developing a more simplified assay that could be used as a prognostic marker for FIV infection. Blood samples from 43 FIV-infected and 25 FIV-negative cats were assayed for the concentration of four acute phase proteins. Both healthy and sick cats were included in the study. Compared to healthy cats, sick cats had significantly higher concentrations of serum amyloid A (P<0.05). Alpha 1-acid glycoprotein and haptoglobin were also found to be in higher concentrations in sick cats (P<0.1). Other variables such as age and gender were also associated with acute phase protein concentrations. With respect to FIV infection, it was found that in sick cats, serum amyloid A, in combination with the age of the cat, was the best predictor of FIV viral RNA load. Alpha 1-acid glycoprotein and haptoglobin were not significantly associated with FIV viral RNA load. Although health status did not influence albumin levels, they were found to be significantly lower in FIV-positive cats in comparison to FIV-negative cats (P<0.05). The frequent monitoring of viral RNA loads and CD4+ lymphocyte counts that is performed on HIV-infected patients is cost prohibitive in veterinary patients. This study showed that there is potential for the use of acute phase protein concentrations (in particular serum amyloid A) as alternative prognostic tools in FIV-infected cats. Further work, particularly longitudinal studies, is required to more definitively define changes in viral RNA load and acute phase protein concentrations throughout the course of FIV infection.

O vírus da imunodeficiência felina (FIV) é um membro da subfamília Lentivirinae da família Retroviridae. A infecção é caracterizada por imunodepressão com um declíneo progressivo dos linfócitos T CD4+, propiciando, desta maneira, o surgimento de infecções oportunistas. Já o vírus da leucemia viral felina (FeLV) pertence a subfamília Oncovirinae da família Retroviridae. Este vírus é um importante patógeno dos gatos domésticos que causa uma variedade de desordens neoplásicas e degenerativas e também apresenta distribuição mundial. O presente estudo compreendeu um levantamento da prevalência das infecções por FIV e FeLV no Município de Porto Alegre. Foram analisadas 65 amostras de gatos sadios e doentes. A detecção destas viroses foi realizada utilizando um “kit” comercial de ELISA para ambas as viroses e um protocolo de reação em cadeia da polimerase aninhada (Nested-PCR) para detecção do FIV. Os resultados demonstraram que 21,5% (14/65) dos gatos foram positivos para FIV combinado os resultados de ambos os testes, 10,8% (7/65) foram positivos para FeLV e 6,1% (4/65) foram positivos para ambos os vírus. Foram também realizados hemogramas de 48 animais, dos quais 8 apresentaram resultados positivos para FIV na Nested-PCR. Através do teste T de Student, verificou-se que não houve diferença significativa nos valores hematológicos destes animais. Conclui-se que a utilização do ELISA com a PCR dobrou a chance de detecção de gatos FIV positivos. Desta forma, a prevalência de FIV foi aproximadamente o dobro do que a de FeLV, ao contrário do que ocorre na maior parte de outros locais estudados. / Feline immunodeficiency virus (FIV) belongs to the Lentivirinae subfamily of the Retroviridae family. The infection is characterized by immunodepression and progressive decline in CD4+ T cells that may render the animal susceptible to opportunistic infections. Feline leukemia virus (FeLV) belongs to subfamily Oncovirinae of the Retroviridae family. The virus also affects domestic cats, being an important pathogen that causes a variety of neoplastic disorders and degenerative diseases. Both viruses have a worldwide distribution. The present study aims to determine the prevalence of infection with FIV and FeLV in Porto Alegre municipality. A total of 65 cats were tested, comprising healthy and sick cats. A commercial ELISA kit was used to detect anti-FIV antibodies and FeLV antigen. A nested polymerase chain reaction (Nested-PCR) was also used for FIV provirus detection. The results showed that 21.5% of the sampled cats were positive for FIV in the ELISA and Nested-PCR, 10.8% were positive for FeLV in the ELISA and 6.1% were positive for both viruses. Haemogram of 48 animals were performed but it was not found any significant association between hematologic values of FIV positive and negative animals. It was concluded that the use of ELISA and Nested-PCR increased the possibility to detect FIV positive cats. The prevalence of FIV infected cats was higher than the prevalence of FeLV positive cats, the opposite of what is normally found in studies performed in other regions.

O vírus da imunodeficiência felina (FIV) é um membro da subfamília Lentivirinae da família Retroviridae. A infecção é caracterizada por imunodepressão com um declíneo progressivo dos linfócitos T CD4+, propiciando, desta maneira, o surgimento de infecções oportunistas. Já o vírus da leucemia viral felina (FeLV) pertence a subfamília Oncovirinae da família Retroviridae. Este vírus é um importante patógeno dos gatos domésticos que causa uma variedade de desordens neoplásicas e degenerativas e também apresenta distribuição mundial. O presente estudo compreendeu um levantamento da prevalência das infecções por FIV e FeLV no Município de Porto Alegre. Foram analisadas 65 amostras de gatos sadios e doentes. A detecção destas viroses foi realizada utilizando um “kit” comercial de ELISA para ambas as viroses e um protocolo de reação em cadeia da polimerase aninhada (Nested-PCR) para detecção do FIV. Os resultados demonstraram que 21,5% (14/65) dos gatos foram positivos para FIV combinado os resultados de ambos os testes, 10,8% (7/65) foram positivos para FeLV e 6,1% (4/65) foram positivos para ambos os vírus. Foram também realizados hemogramas de 48 animais, dos quais 8 apresentaram resultados positivos para FIV na Nested-PCR. Através do teste T de Student, verificou-se que não houve diferença significativa nos valores hematológicos destes animais. Conclui-se que a utilização do ELISA com a PCR dobrou a chance de detecção de gatos FIV positivos. Desta forma, a prevalência de FIV foi aproximadamente o dobro do que a de FeLV, ao contrário do que ocorre na maior parte de outros locais estudados. / Feline immunodeficiency virus (FIV) belongs to the Lentivirinae subfamily of the Retroviridae family. The infection is characterized by immunodepression and progressive decline in CD4+ T cells that may render the animal susceptible to opportunistic infections. Feline leukemia virus (FeLV) belongs to subfamily Oncovirinae of the Retroviridae family. The virus also affects domestic cats, being an important pathogen that causes a variety of neoplastic disorders and degenerative diseases. Both viruses have a worldwide distribution. The present study aims to determine the prevalence of infection with FIV and FeLV in Porto Alegre municipality. A total of 65 cats were tested, comprising healthy and sick cats. A commercial ELISA kit was used to detect anti-FIV antibodies and FeLV antigen. A nested polymerase chain reaction (Nested-PCR) was also used for FIV provirus detection. The results showed that 21.5% of the sampled cats were positive for FIV in the ELISA and Nested-PCR, 10.8% were positive for FeLV in the ELISA and 6.1% were positive for both viruses. Haemogram of 48 animals were performed but it was not found any significant association between hematologic values of FIV positive and negative animals. It was concluded that the use of ELISA and Nested-PCR increased the possibility to detect FIV positive cats. The prevalence of FIV infected cats was higher than the prevalence of FeLV positive cats, the opposite of what is normally found in studies performed in other regions.

Com o objetivo de avaliar a magnitude da infecção por micoplasmas hemotrópicos nos felinos anêmicos, amostras sangüíneas de 270 felinos anêmicos (Ht&le;29%) e 53 felinos saudáveis foram submetidas à exames hematológicos, bioquímicos séricos (proteína total, albumina, fosfatase alcalina, alanina aminotransferase, aspartato aminotransferase, gamaglutamil transferase, bilirrubinas, uréia e creatinina), avaliação citológica do esfregaço sangüíneo e testes moleculares para a detecção de material genético de Mycoplasma spp. Foram encontradas 25 amostras positivas no grupo dos felinos anêmicos, pela técnica de Nested-PCR utilizando-se primers que amplificam fragmentos do gene 16S rRNA dos hemoplasmas. Dentre as amostras positivas, 23 foram caracterizadas por meio de seqüenciamento como Mycoplasma haemofelis e as duas restantes como \"Candidatus Mycoplasma turicensis\" e Mycoplasma haemocanis, respectivamente. As seqüências de nucleotídeos encontradas nesse estudo estão disponíveis no GenBank, sob os números de acesso EU442616 a EU442640, sendo os números EU442629 e EU442623, referentes ao \"Candidatus M. turicensis\" e M. haemocanis, respectivamente. Nos felinos infectados por M. haemofelis a anemia foi mais intensa quando comparados aos animais anêmicos negativos para qualquer uma das espécies de micoplasmas. Quanto à bioquímica sérica, as concentrações das bilirrubinas e a atividade sérica da ALT foram maiores nos felinos infectados. Adicionalmente, com o intuito de avaliar o papel desempenhado pelos retrovírus no desenvolvimento ou agravamento da anemia causada por micoplasmas hemotrópicos, todos os felinos foram avaliados quanto à infecção pelo vírus da imunodeficiência felina (FIV) e da leucemia felina (FeLV), por meio de testes imunoenzimáticos (ELISA) para a detecção de ambos os vírus, de imunofluorescência indireta para detecção do antígeno do FeLV e de técnicas moleculares de detecção do DNA viral do FIV. Dentre os felinos saudáveis não foi observada nenhuma amostra positiva para os micoplasmas hemotrópicos e/ou retrovírus. A associação entre M. haemofelis e FIV (p=0,009) e entre o M. haemofelis e FeLV (p=0,015) , foi evidenciada. O felino infectado por \"Candidatus M. turicensis\" apresentou discreta diminuição do hematócrito e ausência de sinais de regeneração medular e o felino positivo para M. haemocanis apresentou anemia mais profunda com sinais de regeneração. No primeiro a infecção por nenhum dos retrovírus foi identificada, enquanto que o segundo apresentou co-infecção por FIV e FeLV. As informações obtidas das alterações hematológicas e bioquímicas correlacionadas à infecção pelo M. haemofelis evidenciaram o potencial patogênico dessa espécie de micoplasma hemotrópico. A disfunção imunológica resultante da infecção pelos retrovírus pode predispor à infecção por M. haemofelis, não se excluindo a possibilidade de infecção por outros hemoplasmas. / The present study aimed to evaluate the magnitude of the hemotrophic mycoplasmas infections in anemic cats. Samples from 270 anemic cats (PCV&le;29%) and 53 healthy cats were submitted to hematological analysis (CBC, cytologic evaluation of blood smear), serum biochemistry (total protein, albumin, alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, gama glutamil transferase, bilirubins, urea and creatinin), and molecular assays for hemoplasma DNA detection in blood samples. Among the anemic cats, 25 samples were positive by Nested-PCR for the gender Mycoplasma using primers targeting the 16S rRNA. For species identification, sequencing of the products revealed that 23 cats were infected with Mycoplasma haemofelis, one with \"Candidatus M. turicensis\" and another with M. haemocanis. The GenBank accession numbers of the nucleotide sequences derived in this study are from EU442616 to EU442640 (EU442629 and EU442623 refer to \"Candidatus M. turicensis\" and M. haemocanis, respectively). M. haemofelis-infected cats presented significantly more severe anemia and higher bilirubins concentration and ALT serum activity. Additionally, with purpose to evaluate the role play by the retrovirus in the development or aggravation of the anemia caused by hemotrophic mycoplasmas, all cats were tested for FeLV p27 antigenemia by enzyme-linked immunosorbent assay and by indirect immunofluorescence, and anti-FIV antibodies by enzyme-linked immunosorbent assay and viral DNA by Nested-PCR. None of the healthy cats presented infection with hemotrophic mycoplasmas and/or retroviruses. The association between M. haemofelis and retroviruses (FIV, p=0,009 and FeLV, p=0,015) in anemic cats was evidenced. In the \"Candidatus M. turicensis\"-infected cat, slightly decreased hematocrit with no signs of regeneration were observed; and in the M. haemocanis-infected cat anemia was severe and regenerative. In the first, retroviruses infections were not detected, whereas the second was infected with FIV and FeLV. The hematological and biochemistry abnormalities correlated to the M. haemofelis infection had evidenced the pathogenic potential of this hemoplasma species. In conclusion, immunological dysfunction resulting from retrovirus infection may predispose to M. haemofelis infection, without excluding the possibility of infection with other hemoplasma.

O vírus da imunodeficiência felina (FIV) é um membro da subfamília Lentivirinae da família Retroviridae. A infecção é caracterizada por imunodepressão com um declíneo progressivo dos linfócitos T CD4+, propiciando, desta maneira, o surgimento de infecções oportunistas. Já o vírus da leucemia viral felina (FeLV) pertence a subfamília Oncovirinae da família Retroviridae. Este vírus é um importante patógeno dos gatos domésticos que causa uma variedade de desordens neoplásicas e degenerativas e também apresenta distribuição mundial. O presente estudo compreendeu um levantamento da prevalência das infecções por FIV e FeLV no Município de Porto Alegre. Foram analisadas 65 amostras de gatos sadios e doentes. A detecção destas viroses foi realizada utilizando um “kit” comercial de ELISA para ambas as viroses e um protocolo de reação em cadeia da polimerase aninhada (Nested-PCR) para detecção do FIV. Os resultados demonstraram que 21,5% (14/65) dos gatos foram positivos para FIV combinado os resultados de ambos os testes, 10,8% (7/65) foram positivos para FeLV e 6,1% (4/65) foram positivos para ambos os vírus. Foram também realizados hemogramas de 48 animais, dos quais 8 apresentaram resultados positivos para FIV na Nested-PCR. Através do teste T de Student, verificou-se que não houve diferença significativa nos valores hematológicos destes animais. Conclui-se que a utilização do ELISA com a PCR dobrou a chance de detecção de gatos FIV positivos. Desta forma, a prevalência de FIV foi aproximadamente o dobro do que a de FeLV, ao contrário do que ocorre na maior parte de outros locais estudados. / Feline immunodeficiency virus (FIV) belongs to the Lentivirinae subfamily of the Retroviridae family. The infection is characterized by immunodepression and progressive decline in CD4+ T cells that may render the animal susceptible to opportunistic infections. Feline leukemia virus (FeLV) belongs to subfamily Oncovirinae of the Retroviridae family. The virus also affects domestic cats, being an important pathogen that causes a variety of neoplastic disorders and degenerative diseases. Both viruses have a worldwide distribution. The present study aims to determine the prevalence of infection with FIV and FeLV in Porto Alegre municipality. A total of 65 cats were tested, comprising healthy and sick cats. A commercial ELISA kit was used to detect anti-FIV antibodies and FeLV antigen. A nested polymerase chain reaction (Nested-PCR) was also used for FIV provirus detection. The results showed that 21.5% of the sampled cats were positive for FIV in the ELISA and Nested-PCR, 10.8% were positive for FeLV in the ELISA and 6.1% were positive for both viruses. Haemogram of 48 animals were performed but it was not found any significant association between hematologic values of FIV positive and negative animals. It was concluded that the use of ELISA and Nested-PCR increased the possibility to detect FIV positive cats. The prevalence of FIV infected cats was higher than the prevalence of FeLV positive cats, the opposite of what is normally found in studies performed in other regions.

Com o objetivo de avaliar a freqüência de infecção por micoplasmas hemotrópicos em gatos com linfoma e seu impacto na ocorrência de anemias nesses animais, foram analisadas amostras sangüíneas de 14 animais com diagnóstico de linfoma, sem qualquer tratamento prévio e 14 amostras de sangue de gatos hígidos, por meio da técnica de PCR-Nested. Utilizaram-se primers que amplificam fragmentos do gene 16S rRNA dos micoplasmas. Eritrograma e bioquímica sérica foram realizados, assim como testes sorológicos imunoenzimáticos (ELISA) para ambos os retrovírus. Anemia foi observada em 28,6% (4/14) dos gatos com linfoma. Em dois a anemia foi classificada como normocítica normocrômica não regenerativa, e em outros dois como macrocitica normocrômica não regenerativa. A freqüência de infecção pelos micoplasmas hemotrópicos felinos nos gatos com linfoma foi de 7,14% (1/14). Após seqüenciamento e posterior prova de identidade no GenBank, o agente foi identificado como M. haemofelis, número de acesso FJ544859. A freqüência de infecção pelos retrovírus foi de 21,42% para o FeLV e 7,14% (3/14) para o FIV. O animal infectado pelo M. haemofelis não apresentou anemia, ainda que apresentasse infecção concomitante pelo FeLV. O grupo controle não apresentou infecção por micoplasmas ou retrovírus. Nas condições em que este estudo foi realizado, concluiu-se que a anemia observada nos gatos com linfoma não foi ocasionada pela infecção por micoplasmas hemotrópicos, mas provavelmente em decorrência das alterações hematológicas promovidas pelo processo neoplásico, associadas ou não à infecção pelo FeLV. Portanto, a infecção pelos micoplasmas não apresentou um impacto direto na ocorrência de anemias em gatos com linfoma. / To evaluate the frequency of infection by hemotropic mycoplasmas in cats with lymphoma and its impact in the development of anaemia in those animals, blood samples from 14 animals diagnosed with Lymphoma and without any previous treatment and 14 blood samples from healthy cats were analyzed by means of the PCR-Nested technique. Primers were utilized and selectively amplified fragments of 16SrRNA gene of mycoplasma. Haematology, serum biochemical profile and FeLV/FIV ELISA were performed in all 28 cats. Anaemia was observed in 28.6% (4/14) of the cats with lymphoma. In two of them, anaemia was classified as normocytic-normochromic nonregenerative and in the other two as macrocytic-normochromic nonregenerative. The frequency of feline haemotropic mycoplasmas infection in cats with lymphoma was 7.14% (1/14). After sequencing and identity proof by the GenBank, the agent was identified as M. haemofelis, access number FJ544859. The frequency of retrovirus infection among all the cats with lymphoma was 21.42% (3/14) for FeLV and 7.14% (1/14) for FIV. The cat infected by M. haemofelis was also infected with FeLV, but was not anaemic. The 14 cats used as control did not exhibited infection by mycoplasmas or retrovirus infections. Under the conditions in which this study was developed, one can conclude that the anaemia observed in cats with lymphoma may not be related to hemotropic microplasmas infection, but to haematologyc alterations promoted by the associated neoplasic process and/or the occurrence or of FeLV infection. Therefore, the infection by the mycoplasmas did not present a direct impact in the occurrence of anaemies in cats with limphoma.

A infecção de trato respiratório superior em gatos é uma afecção muito frequente em indivíduos que vivem em abrigos, com elevada morbidade e em alguns casos, fatal. O herpesvírus felino tipo1 (FHV-1) e a Chlamydophila felis estão entre os principais causadores. O FHV-1 ocasiona quadros de espirros, secreção nasal e alterações oculares como conjuntivite. A C. felis é responsável pelos piores casos de conjuntivite e apresenta um plasmídeo críptico como possível fator de virulência. A presença dos retrovírus da leucemia felina (FeLV) e/ou imunodeficiência dos felinos (FIV) debilita a função do sistema imunológico, causando imunossupressão e consequentemente aumento no índice de morbidade e mortalidade. Neste trabalho foram avaliados quatro abrigos, três gatis particulares não-comercias (um localizado em Osasco/SP e outros dois São Paulo/SP). Os gatis possuiam alta densidade populacional e a procedência dos gatos alojados era desconhecida. A detecção de FHV-1, como de C. felis e de três genes do plasmídeo criptico foram realizadas por PCR em amostras de mucosa oral e de conjuntiva ocular de ambos os olhos obtidas com swabs de algodão, secos e estéreis. Amostras de sangue foram coletadas para a detecção do FIV e FeLV por meio de teste imunoenzimático. O sintomas clínicos dos animais foram classificados de 1 a 4, sendo 4 atribuído àqueles que apresentavam pior sintomatologia. A ocorrência de FIV e FeLV no 1° gatil foi de 4,63% e 3,70%, no 2° gatil foi de 0% e 6,45%, enquanto que no 3° gatil foi 75% e 0% respectivamente, estes vírus não foram detectados no 4° gatil. FHV-1 foi observado em 61,11% dos gatos no 1° gatil; 90,32% no 2° gatil, 100% no 3° gatil e em 89,74% dos animais do 4° gatil. No 1° gatil, 7,41% das amostras apresentavam C. felis, no 2° gatil, 58,06%; no 4° gatil, 23,08%; enquanto que no 3° gatil o agente não foi detectado. Dentre as amostras positivas para C. felis, os genes do plasmídeo críptico foram detectados; no 1o gatil o gene 1 estava presente em 62,50% das amostras, o gene 2 e 3 em 75%, para o 2° gatil obteve-se 61,11% de positividade para os genes 1 e 2 e 55,56% para o gene 3; no 4° gatil o gene 1 e 3 estavam presentes em 77,78% das amostras, o gene 2 em 55,56%. Os óbitos relatados no período do estudo foram de animais classificados com sintomas 3 ou 4 e positivos para C. felis e para o plasmídeo críptico. No presente trabalho foi observada uma elevada ocorrência de C. felis e de seu plasmídeo críptico, apesar da baixa ocorrência de FIV e FeLV nos gatis. / The infection of upper respiratory disease in cats is very common in individuals that living in shelters, with high morbidity, and in some cases, fatal. The feline herpesvirus type 1 (FHV- 1) and Chlamydophila felis are agents the main causes. The FHV- 1 causes sneezing, nasal discharge and ocular abnormalities such as conjunctivitis. The C. felis is responsible for the worst cases of conjunctivitis and features a cryptic plasmid as a possible virulence factor. The presence of the feline leukemia virus (FeLV) and/or vírus of feline immunodeficiency (FIV) weaken the function of the immune system, causing immunosuppression and therefore increased morbidity and mortality. This study evaluated four shelters, three catteries private non-commercial (one located in Osasco/SP and two in São Paulo/SP). Catteries possessed high population density and cats housed origin was unknown. The detection of FHV- 1 as three genes of the C. felis and cryptic plasmid was performed by PCR in oral mucosa and the ocular conjunctiva of both eyes obtained with cotton swabs, dried and sterile. Blood samples were collected for the detection of FeLV and FIV by enzyme immunoassay. The clinical symptoms of animals were classified from 1 to 4 , with 4 assigned to worst symptoms. The presence of the FIV and FeLV was in the first cattery 4.63% and 3.70%, in the second cattery was 0% and 6.45%, while in the third cattery was 75% and 0%, respectively, these viruses do not were detected in the 4th cattery. FHV- 1 was observed in 61.11 % of the cats in the first cattery; 90.32 % in the second cattery 100 % in the third and 89.74% of the animals of the fourth cattery. In the first cattery, 7.41% of the samples had C. felis, the second cattery, 58.06 %, in the fourth cattery, 23.08%, while the third cattery the agent was not detected. Among the samples positive for C. felis genes were detected cryptic plasmid; in the first cattery, the first gene was present in 62.50%, gene 2 and 3 in 75% of the samples; for the second cattery was obtained 61.11 % positive for 1 and 2 genes and 55.56 % to the third gene; in fourth cattery the first and the third genes were present at 77.78% of the samples in the second gene was in 55.56%. The deaths reported during the study period were classified in animals with symptoms 3 or 4 and positive for C. felis and the cryptic plasmid. In this study we observed a high incidence of C. felis and the cryptic plasmid, despite the low occurrence of FIV and FeLV in catteries.

Made available in DSpace on 2014-08-20T14:37:48Z (GMT). No. of bitstreams: 1 Dissertacao_fabio_silva.pdf: 518189 bytes, checksum: 5328c1b56ef14ad739bd14cb751dcd72 (MD5) Previous issue date: 2012-02-24 / The feline immunodeficiency virus belongs to the Retroviridae family, Lentivirus gennus and presents molecular structure and pathogenicity similar to the human immunodeficiency virus (HIV), therefore it is not transmissible to humans, being susceptible only the domestic and feral cats. FIV is classified in five phylogenetically different subtypes from A to E spread worldwide, apart from recombinant strains among the subtypes. Recently, two new subtypes were described, the subtype F identified in the United States and Portugal, and the subtype U-NZenv in New Zealand. Considering that the retroviruses have the ability to integrate the cell genome, under double stranded DNA form, it is possible to detect the provirus in infected leucocytes through the polymerase chain reaction (PCR) technique. The present report investigated the occurrence of the feline immunodeficiency virus infection between 2010 and 2011 in domestic cats submitted to medical treatment at the Hospital of Veterinary Clinics of the Federal University of Pelotas and private clinics from Pelotas, RS. Blood samples of seventy animals, healthy or sick, were collected and subjected to the nested-PCR technique. The tested cats were classified in two groups taking into account their clinical condition: the group 1 represented 28 FIV suspect cats with lymphadenomegaly, neurological disorders or chronic and recurring infections. The results pointed out a FIV infection frequency of 15,7% (11/70). Eight of the positive samples were subjected to molecular characterization, being all of them into the subtype B. The most diagnosed clinical manifestations in the cats that developed disease related to FIV were bronchopulmonar (4/10) and cutaneous (3/10) secondary infections. Another clinical disorders observed in the positive animals were gingivitis, uveitis, anemia and icterus. The FIV infected cats presented 30% of lethality during the period of study. Most of the infected cats were up to 10 years of age. Faced with the data shown in this report we could conclude that the subtype B of the feline immunodeficiency virus presents circulation in the domestic cat population of the south region of Rio Grande do Sul and elderly animals affected by chronic or recurring infections must be FIV tested. / O vírus da imunodeficiência felina pertence à família Retroviridae, gênero Lentivirus e apresenta estrutura molecular e patogenia similar ao vírus da imunodeficiência humana (HIV), entretanto não é transmissível ao homem, sendo suscetíveis somente os felinos domésticos e selvagens. O FIV é classificado em cinco subtipos filogeneticamente diferentes de A a E, distribuídos mundialmente, além de cepas com recombinações entre os subtipos. Recentemente dois novos subtipos foram descritos, o subtipo F identificado nos Estados Unidos e Portugal, e o subtipo U-NZenv na Nova Zelândia. Considerando-se que os retrovírus têm a capacidade de integrar-se ao genoma celular, sob a forma de DNA de dupla fita, é possível a detecção do provírus em leucócitos infectados, através da técnica de reação em cadeia da polimerase (PCR). O presente trabalho investigou a ocorrência de infecção pelo vírus da imunodeficiência felina, entre os anos de 2010 e 2011, em gatos domésticos levados para atendimento médico no Hospital de Clínicas Veterinária da Universidade Federal de Pelotas e clínicas privadas da cidade de Pelotas, RS. Amostras de sangue de 70 animais, entre hígidos e doentes, foram colhidas e submetidas à técnica de nested-PCR. Os gatos testados foram classificados em dois grupos quanto à condição clínica: o grupo 1 foi representado por 28 felinos suspeitos de FIV, diagnosticados com linfoadenomegalia, sinais neurológicos ou com infecções crônicas e recidivantes; o grupo 2 representado por 42 animais livres de sintomatologia relacionada a FIV. Os resultados apontaram uma frequência de infecção pelo FIV de 15,7% (11/70). Das amostras positivas, 8 foram submetidas à caracterização molecular, sendo todas alocadas dentro do subtipo B. As manifestações clínicas mais diagnosticadas nos felinos que desenvolveram doença relacionada a FIV, foram as infecções secundárias broncopulmonares (4/10) e cutâneas (3/10). Outras alterações clínicas identificadas em animais positivos foram gengivite, uveíte, anemia e icterícia. Os animais infectados por FIV apresentaram letalidade de 30% durante o período de estudo. Em relação à faixa etária a maior proporção de felinos infectados apresentava idade superior a 10 anos. Diante dos dados apresentados conclui-se que o subtipo B do vírus da imunodeficiência felina apresenta circulação na população de gatos domésticos da região sul do Rio Grande do Sul, e que animais idosos acometidos por infecções crônicas ou recidivantes devem ser testados para esse agente.

Thesis (M.Med. (Radiation Oncology)) -- University of Limpopo, 2020 / Introduction Invasive cervical cancer (ICC) constitutes almost 50% of all cancer conditions diagnosed and treated at the Polokwane/Mankweng Hospital Complex (PMHC). HIV infection is also a very common condition. There is no consensus on the relationship between the two clinical conditions among patients treated at PMHC. There is a need to describe the simultaneous occurrence of the two clinical conditions among these patients to define a rational approach to these conditions’ clinical management. Methodology This was a retrospective review of medical records of patients diagnosed with ICC who were treated at PMHC in Limpopo Province, South Africa in 2013. Results Three hundred and twenty-nine medical records were reviewed in this study; 64% of the patients were HIV-negative, and only 35% were HIV-positive. Thirty-five percent of the patients were younger than 50 years of age, followed by those aged 50–59 years (23%). Among women in the age group 30–59 years, the most common ICC stages were IIB and IIIB. In women older than 60 years, stages IIB, IIIA, IIIB and IVA were the most common. In the HIV-positive women, 18% had a CD4 cell count of less than 200/μL, compared to 2% in the HIV-negative women (p <0.05). Among the HIV-negative women, stages IIIB (49.8%) and IIB (24.6%) were the most common, where as among those who were HIV-positive, stages IIIB (55.6%) and IIB (22.6%) dominated. Conclusion This retrospective study did not find any relationship between HIV infection and ICC in patients treated at PMHC. However, it indicated that a significant proportion of HIV-positive women with ICC had lower CD4 cell counts compared to those of HIV-negative women. KEY CONCEPTS: Invasive cervical cancer, Human immunodeficiency virus, Stage, Prevalence, CD4 cell count, Age, Polokwane/Makweng Hospital Complex

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