RESUMO
Staphylococcus aureus nasal carriage is a common condition affecting both healthy and immunocompromised populations and provides a reservoir for dissemination of potentially infectious strains by casual contact. The factors regulating the onset and duration of nasal S. aureus colonization are mostly unknown, and a human-relevant animal model is needed. Here, we screened 17 pig-tailed macaques (Macaca nemestrina) for S. aureus carriage, and 14 of 17 animals tested positive in the nose at one or both screening sessions (8 weeks apart), while the other 3 animals were negative in the nose but positive in the pharynx at least once. As in humans, S. aureus colonization was densest in the nose, and treatment of the nostrils with mupirocin ointment effectively cleared the nostrils and 6 extranasal body sites. Experimental nasal S. aureus colonization was established with 104 CFU/nostril, and both autologous and nonautologous strains survived over 40 days without any apparent adverse effects. A human nasal S. aureus isolate (strain D579, sequence type 398) was carried in 4 of 6 animals for over 3 weeks. Nostrils that did eradicate experimentally applied S. aureus exhibited neutrophilic innate immunity marked by elevated nasal interleukin-1ß (IL-1ß), IL-8, and monocyte chemotactic protein 1 levels and a 10-fold decreased IL-1 receptor antagonist/IL-1ß ratio within 7 days postinoculation, analogous to the human condition. Taken together, pig-tailed macaques represent a physiological model of human S. aureus nasal carriage that may be utilized for testing natural colonization and decolonization mechanisms as well as novel classes of anti-S. aureus therapeutics.
Assuntos
Macaca nemestrina/microbiologia , Nariz/microbiologia , Staphylococcus aureus/fisiologia , Animais , Portador Sadio , Feminino , GenótipoRESUMO
An adult, female, pig-tailed macaque (Macaca nemestrina) of Indonesian origin presented with profound weight loss, anemia (PCV, 29%; normal, 36% to 45%), hypoalbuminemia (1.0 g/dL; normal, 3.5 to 5.2 g/dL), elevated alkaline phosphatase (1990 U/L; normal, 26 to 98 U/L), and an elevated erythrocyte sedimentation rate (75 mm/h; normal, less than 20 mm/h). Abdominal ultrasonography demonstrated an enlarged liver with hyperechoic areas. Euthanasia was performed. Grossly, the liver had multifocal, effacing, white masses throughout and was enlarged with rounded edges. There were 2, small nodules in the right lung lobes. Histologically, the hepatic masses were densely fibrous-encapsulated granulomas with vast central necrosis. The lung nodules also were maturing granulomas, and one kidney and one atrium had small, early granulomas. Fite acid-fast stains of liver and lung revealed very few acid-fast bacilli. PCR analysis of paraffin-embedded liver identified Mycobacterium tuberculosis complex. Culture of the liver was negative twice. This macaque had 16 negative intradermal tuberculin skin tests over the course of 6 y. We hypothesize that the animal arrived with a latent hepatic or enteric infection that later recrudesced and disseminated. Primary hepatic mycobacteriosis is not a typical presentation of tuberculosis in macaques. Negative tuberculin skin tests can be seen with latent infections and extrapulmonary tuberculosis such as Pott disease. This case underscores the problems associated with current surveillance procedures and the risks associated with latent mycobacterial infections in macaques.
Assuntos
Hepatomegalia/veterinária , Macaca nemestrina/microbiologia , Doenças dos Macacos/patologia , Mycobacterium tuberculosis/fisiologia , Tuberculose/veterinária , Animais , Feminino , Hepatomegalia/patologia , Pulmão/patologia , Pneumopatias/diagnóstico , Pneumopatias/patologia , Pneumopatias/veterinária , Doenças dos Macacos/diagnóstico , Tuberculose/diagnóstico , Tuberculose/patologiaRESUMO
Traumatic wounds and access to outdoor enclosures containing soil contribute to development of tetanus in nonhuman primates. A retrospective, matched case-control study was conducted at a primate center to evaluate these factors by analysis of medical records of animals sustaining traumatic injuries during a 3-yr study period. Thirty-one macaques with traumatic injuries and a clinical diagnosis of tetanus were selected as cases, and 62 macaques with traumatic injuries and no diagnosis of tetanus were selected as controls. For an animal with injuries to the digits, the odds of developing tetanus were 9.6 times those of a similar animal without injuries to the digits (Odds Ratio [OR] = 9.55, 95% CI = 1.56-58.59); with injuries to the tail, the odds of developing tetanus were 8.0 times those of a similar animal without injuries to the tail (OR = 7.95, 95% CI = 0.82-77.04); and with injuries in more than one location, the odds of developing tetanus were 8.5 times those for a similar animal with injuries in just one location (OR = 8.45, 95% CI = 1.01-70.46). A nonhuman primate with injuries to the leg was less likely to develop tetanus than a similar nonhuman primate without injuries to the leg (OR = 0.19, 95% CI = 0.03-1.2). Results indicated that wound location is associated with development of tetanus infection in rhesus macaques. Identification of high-risk trauma cases will allow better allocation of wound management and tetanus prophylaxis in institutions, especially in those housing nonhuman primates outdoors.
Assuntos
Extremidades/lesões , Macaca , Doenças dos Macacos/patologia , Tétano/veterinária , Ferimentos e Lesões/veterinária , Animais , Animais de Zoológico/lesões , Estudos de Casos e Controles , Extremidades/microbiologia , Análise Fatorial , Feminino , Macaca/lesões , Macaca/microbiologia , Macaca mulatta/lesões , Macaca mulatta/microbiologia , Macaca nemestrina/lesões , Macaca nemestrina/microbiologia , Masculino , Razão de Chances , Estudos Retrospectivos , Fatores de Risco , Tétano/patologia , Ferimentos e Lesões/microbiologia , Ferimentos e Lesões/patologiaRESUMO
The subjects of the study were 1,249 primates of different species, kept in a nursery in the city of Adler. The subjects varied in age, were either clinically healthy, diseased, or dead (the death had been caused by an acute intestinal disease). Biological, molecular-genetic (PCR), and immunological (coagglutination reaction) methods were used in diagnostics of campilobacter infections. The study found campilobacter in 20.9% of healthy animals on the average; this number varied depending on the species and age. The frequency of campilobacter infection in diseased and dead animals was higher than that in healthy ones (40.1% and 20.9%, respectively.) Two types of Campilobacter were identified: C. jejuni (73.4% of cases), and C. coli (14.2%). Clinical and pathomorphological manifestations of campilobacteriosis in primates and humans are similar. The portion of campilobacteriosis in acute intestinal diseases of primates is 40.1%.
Assuntos
Infecções por Campylobacter , Campylobacter coli , Campylobacter jejuni , Enteropatias/microbiologia , Primatas/microbiologia , Animais , Callithrix/microbiologia , Infecções por Campylobacter/diagnóstico , Infecções por Campylobacter/microbiologia , Campylobacter coli/isolamento & purificação , Campylobacter jejuni/isolamento & purificação , Interpretação Estatística de Dados , Modelos Animais de Doenças , Humanos , Macaca fascicularis/microbiologia , Macaca mulatta/microbiologia , Macaca nemestrina/microbiologia , Papio anubis/microbiologia , Papio hamadryas/microbiologiaRESUMO
Preclinical studies of topical microbicide products, using appropriate animal models for assessing the safety of repeated use are essential. The pig-tailed macaque (Macaca nemestrina) model has been used to assess the safety of vaginally and rectally applied topical microbicide products. The availability of sexually mature female pig-tailed macaques has become extremely restricted. Currently, M. fascicularis is more readily available, and was therefore evaluated as an alternative model for topical microbicide pre-clinical evaluation. Twenty sexually mature M. fascicularis were assessed for feasibility to mimic the established models. The rectal and cervicovaginal microenvironments of the M. fascicularis were determined to be similar to those of M. nemestrina and humans. The gross anatomy was significantly smaller than that of the pig-tailed macaque, such that colposcopic examinations and multiple biopsies would not be possible. Thus, the M. fascicularis may not be useful for vaginally applied topical microbicide safety studies yet adequate for assessing safety of rectally applied topical microbicide products.
Assuntos
Anti-Infecciosos Locais/normas , Macaca fascicularis/microbiologia , Macaca nemestrina/anatomia & histologia , Modelos Animais , Animais , Avaliação Pré-Clínica de Medicamentos/veterinária , Feminino , Concentração de Íons de Hidrogênio , Macaca fascicularis/anatomia & histologia , Macaca nemestrina/microbiologia , Reto/anatomia & histologia , Reto/microbiologia , Vagina/anatomia & histologia , Vagina/microbiologiaRESUMO
Helicobacter nemestrinae Bronsdon et al. 1991, a gastric helicobacter species isolated from a pigtailed macaque, is thought to be the species most closely related to the important human pathogen Helicobacter pylori. The only available strain of this taxon is the type strain, ATCC 49396T. We sequenced seven housekeeping genes and two flagellin genes for H. nemestrinae ATCC 49396T. If ATCC 49396T were a separate species, these sequences should have been distinct from those of H. pylori. Instead, all sequences clustered together with sequences obtained previously for 20 or more H. pylori isolates from diverse geographical locations. The 16S rDNA sequence differed from that reported previously for this strain by 38 nucleotides and was most similar to that of H. pylori 85D08 (accession no. U00769), which was isolated from a rhesus macaque. It differed by less than 1% from 16S rDNA sequences of numerous other H. pylori strains, including the type strain, NCTC 11637T (= ATCC 43504T). These data indicate that the strain currently distributed as H. nemestrinae ATCC 49396T is really a strain of H. pylori and that H. nemestrinae Bronsdon et al. 1991 is a junior heterotypic synonym of Helicobacter pylori (Marshall et al. 1985) Goodwin et al. 1989.
Assuntos
Helicobacter/classificação , Macaca nemestrina/microbiologia , Animais , DNA Bacteriano/química , DNA Ribossômico/química , Flagelina/genética , Genes Bacterianos , Helicobacter/genética , Helicobacter pylori/classificação , Dados de Sequência Molecular , Filogenia , RNA Ribossômico 16S/química , Análise de Sequência , Especificidade da EspécieRESUMO
We have examined both the sequence changes in the LTR, gag, vif, vpr, vpx, tat, rev, vpu, env, and nef genes and the cell tropism of a cell-free stock of chimeric simian-human immunodeficiency virus (SHIV) isolated from the cerebrospinal fluid of a pig-tailed macaque (PNb) that developed AIDS. This virus (SHIVKU-1) is highly pathogenic when inoculated into other macaques. DNA sequence analysis of PCR-amplified products revealed a total of 5 nucleotide changes in the LTR while vif had 2 consensus amino acid changes. The gag, vif, and vpx had no consensus amino acid substitutions, whereas vpr had 1 consensus substitution. The tat and rev genes of the HXB2 region of SHIVKU-1 had 2 and 1 consensus amino acid changes, respectively. The vpu gene of the HXB2 region of SHIV, which originally had an ACG at the beginning of the gene, reverted to an initiation ATG codon and in addition contained a consensus amino acid substitution at position 69 of this protein. As expected, the majority of the nucleotide substitutions were found in the env and nef genes. Thirteen and 5 amino acid changes were predicted for the corresponding Env and Nef proteins, respectively. In addition, one-third of the env gene clones isolated from the SHIVKU-1 stock had a 5-amino-acid deletion in the V4 region. Using three independent assays, we determined that the changes in the SHIVKU-1 were associated with an increase in the efficiency of replication in macrophages. The strikingly few consensus changes in the virus suggest that conversion of this virus to one capable of causing AIDS in pig-tailed macaques was associated with relatively few changes in the viral envelope and/or accessory genes. These results will provide the basis for the development of a pathogenic, molecular clone of SHIV capable of causing AIDS in pig-tailed macaques.
Assuntos
HIV-1/genética , Síndrome de Imunodeficiência Adquirida dos Símios/microbiologia , Vírus da Imunodeficiência Símia/genética , Síndrome da Imunodeficiência Adquirida/microbiologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Quimera , Clonagem Molecular , Genes Virais , HIV-1/patogenicidade , Macaca nemestrina/microbiologia , Macrófagos/microbiologia , Dados de Sequência Molecular , Vírus da Imunodeficiência Símia/patogenicidade , Especificidade da Espécie , Linfócitos T/microbiologia , Proteínas Estruturais Virais/genética , Replicação ViralRESUMO
Heat-stable (HS, O-antigen) and heat-labile (HL) serotyping are the most common methods used to type Campylobacter jejuni and C. coli for epidemiologic purposes. In this study, we conducted RRNA analysis to differentiate strains of C. jejuni and C. coli that had been serotyped by use of the passive hemagglutination (heat-stable) and slide agglutination (heat-labile) methods. Ribotyping of isolates within HS and HL serotypes revealed further discrimination of strains. Four ribotypes were identified by Pvu II and Pst I digests of eight HS serotype-34 isolates. Ribotyping also differentiated strains within HL serotypes. Ribotyping also was conducted on 10 representative isolates of C. jejuni and C. coli isolated from an infant macaque. The eight ribotypes confirmed previous results of serotyping and other phenotypic analyses, which indicated that the infant was repeatedly reinfected with different strains of C. jejuni and C. coli. Results of the study indicated that ribotyping is a sensitive molecular marker for distinguishing strains of C. jejuni and C. coli. Furthermore, some isolates with similar ribotype patterns had variability in their HS and HL serotypes.
Assuntos
Campylobacter coli/genética , Campylobacter jejuni/genética , Macaca nemestrina/microbiologia , RNA Bacteriano/análise , RNA Ribossômico/análise , Animais , Campylobacter coli/classificação , Campylobacter coli/isolamento & purificação , Campylobacter jejuni/classificação , Campylobacter jejuni/isolamento & purificação , Desoxirribonucleases de Sítio Específico do Tipo II , Temperatura Alta , Antígenos O , Polissacarídeos Bacterianos/análise , SorotipagemRESUMO
To elucidate sites of SRV-2/W persistence, tissue DNA from three groups of naturally infected Macaca nemestrina was analyzed for provirus: vertically transmitted, viremic, seronegative macaques; horizontally transmitted, viremic, seronegative macaques, and nonviremic seropositive macaques. In viremic animals infected vertically, provirus was found in many tissues, whereas in those infected horizontally, proviral DNA was limited. In V-Ab+ macaques, provirus was detected in bone marrow and/or ileocecal junction, confirming the presence of provirus in V-Ab+ animals.
Assuntos
Macaca nemestrina/microbiologia , Doenças dos Macacos/microbiologia , Infecções por Retroviridae/veterinária , Retrovirus dos Símios/isolamento & purificação , Infecções Tumorais por Vírus/veterinária , Animais , DNA Viral/análise , Feminino , Masculino , Doenças dos Macacos/epidemiologia , Prevalência , Provírus/isolamento & purificação , Infecções por Retroviridae/epidemiologia , Infecções por Retroviridae/microbiologia , Retrovirus dos Símios/genética , Retrovirus dos Símios/imunologia , Estudos Soroepidemiológicos , Síndrome de Imunodeficiência Adquirida dos Símios/epidemiologia , Infecções Tumorais por Vírus/epidemiologia , Infecções Tumorais por Vírus/microbiologia , Viremia/microbiologia , Viremia/veterináriaRESUMO
The non-human primate Macaca nemestrina was evaluated for use as a potential model in periodontal research by study of 16 animals. Using one incisor, premolar, and molar per quadrant, we measured supragingival plaque, severity of gingival inflammation, and pocket depth, and analyzed the subgingival flora. Serum IgG titers and avidities to antigens of Porphyromonas gingivalis (Pg) and Actinobacillus actinomycetemcomitans (Aa) were also assessed. Ten animals were between 13 and 24 years old, and six were between 4 and 5 years old. While mean gingival inflammation scores were significantly higher for older than for younger animals (2.2 vs 1.8, p < 0.05), mean plaque index scores and mean probing depths did not differ significantly. The animals harbored a subgingival microflora considered to be pathogenic for humans including Aa, Pg, Bacteroides forsythus, Prevotella intermedia I and II, Campylobacter recta and Fusobacterium nucleatum. Aa, however, was found only in the younger animals. All of the animals had serum IgG antibodies reactive with antigens of Pg and Aa, and titers for Pg but not for Aa were significantly higher in the older relative to the younger animals (t test p < 0.02). In contrast, antibody avidity did not significantly differ between the two groups. A combined clinical assessment index based on maximum probing depth, gingival index score, and tooth loss was used to assess the overall disease severity. Titers were positively associated with disease severity (Spearman's rank correlation 0.57, p = 0.02).(ABSTRACT TRUNCATED AT 250 WORDS)
Assuntos
Modelos Animais de Doenças , Macaca nemestrina/microbiologia , Periodontite/microbiologia , Fatores Etários , Aggregatibacter actinomycetemcomitans/isolamento & purificação , Animais , Anticorpos Antibacterianos/sangue , Afinidade de Anticorpos , Bacteroides/isolamento & purificação , Campylobacter/isolamento & purificação , Fusobacterium nucleatum/isolamento & purificação , Imunoglobulina G/análise , Índice Periodontal , Periodontite/imunologia , Porphyromonas gingivalis/isolamento & purificaçãoRESUMO
Sera from 510 macaques consisting of Macaca mulatta, Macaca assamensis, Macaca fascicularis, Macaca nemestrina, and Macaca arctoides were investigated for antibodies to simian AIDS type D retrovirus (SRV) by ELISA and Western blot with viral antigens purified from supernatants of SRV-1 infected cell cultures. Of these monkeys, 104 were seropositive by ELISA; only 23 were confirmed by Western blot. The true positive reaction to SRV was found in 15 of 463 (3.2%) M. mulatta and eight of eleven (72.7%) M. assamensis.
Assuntos
Anticorpos Antivirais/sangue , Macaca/imunologia , Macaca/microbiologia , Retrovirus dos Símios/imunologia , Animais , China , Macaca fascicularis/imunologia , Macaca fascicularis/microbiologia , Macaca mulatta/imunologia , Macaca mulatta/microbiologia , Macaca nemestrina/imunologia , Macaca nemestrina/microbiologia , Testes de Neutralização , Retrovirus dos Símios/classificação , Retrovirus dos Símios/isolamento & purificação , Sorotipagem , Especificidade da EspécieAssuntos
Síndrome de Imunodeficiência Adquirida dos Símios/prevenção & controle , Vírus da Imunodeficiência Símia/imunologia , Vacinação , Vacinas de Produtos Inativados/imunologia , Vacinas Sintéticas/imunologia , Vacinas Virais/imunologia , Animais , Cercocebus atys/microbiologia , DNA Viral , Transfusão de Linfócitos , Linfócitos/microbiologia , Macaca mulatta/microbiologia , Macaca nemestrina/imunologia , Macaca nemestrina/microbiologia , Provírus , Síndrome de Imunodeficiência Adquirida dos Símios/imunologia , Vírus da Imunodeficiência Símia/isolamento & purificaçãoRESUMO
After observations that Macaca nemestrina were exceptionally susceptible to simian immunodeficiency virus and human immunodeficiency virus type-2 (HIV-2), studies of HIV-1 replication were initiated. Several strains of HIV-1, including a recent patient isolate, replicated in vitro in peripheral blood mononuclear cells (PBMCs) and in CD4-positive M. nemestrina lymphocytes in a CD4-dependent fashion. Eight animals were subsequently inoculated with either cell-associated or cell-free suspensions of HIV-1. All animals had HIV-1 isolated by cocultivation, had HIV-1 DNA in their PBMCs as shown by polymerase chain reaction, and experienced sustained seroconversion to a broad spectrum of HIV-1 proteins. Macaca nemestrina is an animal model of HIV-1 infections that provides opportunities for evaluating the pathogenesis of acute HIV-1 replication and candidate vaccines and therapies.
Assuntos
Genes gag , Infecções por HIV/fisiopatologia , HIV-1/fisiologia , Macaca nemestrina/microbiologia , Replicação Viral , Animais , Sequência de Bases , Antígenos CD4/fisiologia , Cisteína/metabolismo , Bases de Dados Factuais , Soropositividade para HIV , HIV-1/isolamento & purificação , HIV-1/patogenicidade , Humanos , Linfócitos/imunologia , Linfócitos/fisiologia , Metionina/metabolismo , Dados de Sequência Molecular , Oligodesoxirribonucleotídeos , Sondas de Oligonucleotídeos , Proteínas Virais/biossíntese , Proteínas Virais/isolamento & purificaçãoRESUMO
A new microaerophilic, spirally curved, rod-shaped bacterium was isolated from the gastric mucosa of a pigtailed macaque (Macaca nemestrina). The gram-negative cells of this bacterium are oxidase, catalase, and urease positive and strongly resemble Helicobacter pylori (Campylobacter pylori) cells. Like H. pylori, this organism does not metabolize glucose, does not reduce nitrate or produce indole, does not produce H2S from triple sugar iron agar, does not hydrolyze hippurate or esculin, and does not grow in the presence of 1% glycine, 1.5% salt, or 1% bile. Also like H. pylori, it is resistant to nalidixic acid and susceptible to cephalothin. However, unlike H. pylori, the colorless colonies are flat and have irregular edges. This organism has a unique cellular fatty acid composition, forming a new gas-liquid chromatography group, group K, and a distinctive DNA content (24 mol% guanine plus cytosine). It exhibits less than 10% DNA-DNA homology (as determined by the nylon filter blot method at 65 degrees C) with other members of the genus Helicobacter. Although the levels of DNA relatedness between previously described Helicobacter species and the new organism are low (less than 10%) and the difference in guanine-plus-cytosine content is large (24 versus 36 to 41 mol%), the genus Helicobacter is the only genus in which it is logical to include the organism at this time. We propose that our single strain represents a new species, Helicobacter nemestrinae, and we designate strain T81213-NTB (= ATCC 49396) as the type strain.
Assuntos
Mucosa Gástrica/microbiologia , Bactérias Anaeróbias Gram-Negativas/classificação , Macaca nemestrina/microbiologia , Animais , Técnicas de Tipagem Bacteriana , Composição de Bases , DNA Bacteriano/análise , Bactérias Anaeróbias Gram-Negativas/citologia , Bactérias Anaeróbias Gram-Negativas/isolamento & purificação , Bactérias Anaeróbias Gram-Negativas/fisiologia , Terminologia como AssuntoRESUMO
A prospective bacteriologic study of 18 infant pig-tailed macaques (Macaca nemestrina) housed in a nursery facility in which Campylobacter spp. are endemic was undertaken to determine the epidemiology of infection and reinfection. The isolates of Campylobacter jejuni and C. coli cultured from 8 of the 18 infants were characterized by serotyping, DNA hybridization, and polyacrylamide gel electrophoresis protein profiles. The chronology of infection was indicative of multiple reinfections with different strains of C. jejuni and C. coli during the 12-month study of each infant. The duration of infection with a particular strain was 3 to 4 weeks. Infants were also infected with nalidixic acid-resistant campylobacters. These observations indicated that long-term infections under endemic conditions are caused by continual reinfection. C. jejuni or C. coli infection correlated with diarrhea in 5 of the 18 infants at 1 to 4 months of age.
Assuntos
Infecções por Campylobacter/veterinária , Macaca nemestrina/microbiologia , Macaca/microbiologia , Criação de Animais Domésticos , Animais , Animais de Laboratório/microbiologia , Animais Recém-Nascidos/microbiologia , Campylobacter/isolamento & purificação , Infecções por Campylobacter/complicações , Infecções por Campylobacter/epidemiologia , Campylobacter fetus/isolamento & purificação , Sondas de DNA , Diarreia/microbiologia , Diarreia/veterinária , Doenças dos Macacos/epidemiologia , Doenças dos Macacos/microbiologia , Estudos Prospectivos , Recidiva , SorotipagemRESUMO
A rapid, sensitive and specific antigen capture (AC) assay has been established for the detection of p27 core protein of SAIDS type-D retrovirus (SRV). SRV p27 antigen in test samples was identified on rabbit anti-p27 IgG-coated microtiter plates by the addition of biotinylated rabbit anti-p27 IgG. This assay was specific for the p27 core protein of SRV-1 and SRV-2 and provided semi-quantitative results in less than 7 hours. Results of the AC assay were highly correlated with those of reverse transcriptase (RT), immunofluorescence and immunoblotting assays. However, the AC assay was faster and more sensitive than the other three assays. The AC assay also provided a rapid diagnostic tool for the detection of SRV in plasma, serum and peripheral blood lymphocyte cocultures. In addition to mass screening of SRV infection in macaque colonies, the AC assay also will be valuable for monitoring the efficacy of antiretroviral agents against SRV in vitro and in vivo.
Assuntos
Antígenos Virais/análise , Macaca nemestrina/microbiologia , Macaca/microbiologia , Doenças dos Macacos/diagnóstico , Infecções por Retroviridae/veterinária , Vírus da Imunodeficiência Símia/imunologia , Animais , Antígenos Virais/sangue , Linhagem Celular , Eletroforese em Gel de Poliacrilamida , Epitopos , Imunofluorescência , Immunoblotting , Macaca mulatta/microbiologia , Infecções por Retroviridae/diagnóstico , Vírus da Imunodeficiência Símia/isolamento & purificaçãoRESUMO
Experimental infection of four specific-pathogen-free Macaca nemestrina monkeys (aged 3.5 and 4.5 months) with Campylobacter jejuni 81-176 caused acute diarrheal illness, characterized by fluid diarrhea, bloody stools, and fecal leukocytes, which lasted for approximately 7 to 11 days. Histologic examination of intestinal biopsies showed acute colitis characterized by infiltration of the mucosa with neutrophils and lymphocytes, and cryptitis. There were no histologic changes in the small intestine. Excretion of C. jejuni was demonstrated for 2 to 4 weeks postchallenge. Plasma antibodies to C. jejuni group antigen were elevated after challenge. Only mild diarrhea occurred after rechallenge with the same strain or with a heterologous C. jejuni strain (79-168) followed by further elevation in specific immunoglobulins A, M, and G. Four 1-year-old juvenile M. nemestrina monkeys which had experienced multiple infections with Campylobacter spp. did not exhibit illness when challenged with C. jejuni 81-176. All had elevated immunoglobulin A, M, and G plasma antibodies prior to challenge, and these humoral antibody levels were indicative of the immunity to challenge. The results demonstrate that C. jejuni infection in M. nemestrina caused colitis with clinical and pathologic results similar to those found in humans and indicate that prior infection protects against subsequent challenge.
Assuntos
Infecções por Campylobacter/fisiopatologia , Colite/fisiopatologia , Macaca nemestrina/microbiologia , Macaca/microbiologia , Animais , Anticorpos Antibacterianos/biossíntese , Infecções por Campylobacter/imunologia , Infecções por Campylobacter/patologia , Campylobacter fetus , Colite/imunologia , Colite/patologia , Colo/patologia , Modelos Animais de Doenças , Fezes/microbiologia , Imunoglobulina A/sangue , Imunoglobulina G/sangue , Imunoglobulina M/sangueRESUMO
A primate lymphotropic lentivirus was isolated on Hut 78 cells after cocultivation of a lymph node from a macaque that died with malignant lymphoma. In earlier studies SIV/Mne was inoculated into 17 macaques and two baboons. All of the macaques became viremic and seropositive. Fifteen of the macaques succumbed to a classic AIDS-like disease, whereas the baboons did not become viremic. The SIV/Mne virus has now been molecularly cloned and inoculated into Macaca nemestrina and baboons. A new transmission study has been initiated to test the effects of route and dosage on disease.
Assuntos
Macaca/microbiologia , Doenças dos Macacos/transmissão , Papio/microbiologia , Infecções por Retroviridae/veterinária , Vírus da Imunodeficiência Símia/fisiologia , Animais , Anticorpos Antivirais/biossíntese , Western Blotting , Clonagem Molecular , Modelos Animais de Doenças , Ensaio de Imunoadsorção Enzimática , Macaca mulatta/microbiologia , Macaca nemestrina/microbiologia , Doenças dos Macacos/imunologia , Infecções por Retroviridae/imunologia , Infecções por Retroviridae/transmissão , Vírus da Imunodeficiência Símia/genética , Vírus da Imunodeficiência Símia/imunologia , Viremia/veterináriaRESUMO
The virulence of three isolates of simian immunodeficiency virus from African green monkeys (SIVagm) was studied in rhesus and pigtailed macaques. None of 15 rhesus monkeys and one of four pigtailed monkeys died from infection during the time they were studied (up to 33 months). SIVagm was only isolated from rhesus monkeys for up to 2 months after inoculation. However, when these animals were secondarily infected with Simian acquired immunodeficiency syndrome retrovirus type 1 (SRV-1), SIVagm was activated and isolated. Dual infection caused increased mortality.