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1.
Lipids ; 48(9): 863-8, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23733443

ABSTRACT

The aim of this study was to determine if changes in omega-3 polyunsaturated fatty acid status following tuna oil supplementation correlated with changes in scores of depression. A total of 95 volunteers receiving treatment for major depression were randomised to consume 8 × 1 g capsules per day of HiDHA (2 g DHA, 0.6 g EPA and 10 mg Vitamin E) or olive oil (placebo) for 16 weeks, whilst undergoing weekly counseling sessions by trained clinical psychologists using a standard empirically validated psychotherapy. Depression status was assessed using the 17 item Hamilton rating scale for depression and the Beck Depression Inventory by a psychodiagnostician who was blind to the treatment. Blood was taken at baseline and 16 weeks (n = 48) for measurement of erythrocyte fatty acids. With HiDHA supplementation, erythrocyte DHA content rose from 4.1 ± 0.2 to 7.9 ± 0.4 % (mean ± SEM, p < 0.001) of total fatty acids but did not change (4.0 ± 0.2 to 4.1 ± 0.2 %) in the olive oil group. The mean changes in scores of depression did not differ significantly between the two groups (-12.2 ± 2.1 for tuna oil and -14.4 ± 2.3 for olive oil). However, analysis of covariance showed that in the fish oil group there was a significant correlation (r = -0.51) between the change in erythrocyte DHA and the change in scores of depression (p < 0.05). Further study of the relationship between DHA and depression is warranted.


Subject(s)
Depressive Disorder, Major/blood , Depressive Disorder, Major/drug therapy , Docosahexaenoic Acids/blood , Erythrocytes/metabolism , Adolescent , Adult , Aged , Capsules , Combined Modality Therapy , Depressive Disorder, Major/therapy , Dietary Supplements , Docosahexaenoic Acids/administration & dosage , Eicosapentaenoic Acid/administration & dosage , Female , Humans , Male , Middle Aged , Olive Oil , Plant Oils/administration & dosage , Psychiatric Status Rating Scales , Psychotherapy/methods , Time Factors , Treatment Outcome , Vitamin E/administration & dosage , Vitamins/administration & dosage , Young Adult
2.
Dev Comp Immunol ; 38(4): 475-86, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22929957

ABSTRACT

Research into marsupial adaptive immunity during ontogeny has been hampered by the lack of antibodies that react to marsupial immunological cell populations. In this study, newly synthesised polyclonal antibodies to the T cell marker, CD8, have been developed and used to investigate the ontogeny and distribution of this T cell population in the tammar wallaby. Immunohistochemical analysis indicated that the distribution of the CD8 lymphocytes in the lymphoid tissues of tammar neonates during the first 144 days of pouch life was similar to that of the eutherian mammals. However, CD8α(+) lymphocytes were observed in the intestines of tammar neonates prior to their first appearance in the cervical thymus, an observation that has not been found in eutherians. A dual labelling immunohistochemical approach was used for the indirect demonstration of CD4 and enabled the simultaneous detection in the tammar wallaby tissues of the two major T-lymphocyte populations, CD4 and CD8 that are associated with adaptive immunity. As in eutherian mammals, CD4(+) cells were the predominant T cell lymphocyte subset observed in the spleen while in the nodal tissues, an age-related decrease in the CD4(+)/CD8(+) ratio was noted. These antibodies provide a new immunological tool to study the role of T cell subsets in marsupial immunity and disease pathogenesis studies.


Subject(s)
CD4-Positive T-Lymphocytes/metabolism , CD8-Positive T-Lymphocytes/metabolism , Lymphoid Tissue/cytology , Macropodidae/growth & development , Adaptive Immunity/physiology , Animals , Animals, Newborn , Antibodies/chemistry , Antibody Specificity , Goats , Immunohistochemistry , Intestines/cytology , Intestines/growth & development , Lymph Nodes/cytology , Lymph Nodes/growth & development , Lymphoid Tissue/growth & development , Macropodidae/immunology , Spleen/cytology , Spleen/growth & development , Thymus Gland/cytology , Thymus Gland/growth & development
3.
Microbiology (Reading) ; 156(Pt 3): 798-808, 2010 03.
Article in English | MEDLINE | ID: mdl-19833775

ABSTRACT

Marsupial mammals, born in an extremely atricial state with no functional immune system, offer a unique opportunity to investigate both the developing microbiome and its relationship to that of the mother and the potential influence of this microbiome upon the development of the immune system. In this study we used a well-established marsupial model animal, Macropus eugenii, the tammar wallaby, to document the microbiome of three related sites: the maternal pouch and saliva, and the gastrointestinal tract (GIT) of the young animal. We used molecular-based methods, targeting the 16S rDNA gene to determine the bacterial diversity at these study sites. In the maternal pouch, 41 unique phylotypes, predominantly belonging to the phylum Actinobacteria, were detected, while in the saliva, 48 unique phylotypes were found that predominantly belonged to the phylum Proteobacteria. The GIT of the pouch young had a complex microbiome of 53 unique phylotypes, even though the pouch young were still permanently attached to the teat and had only been exposed to the external environment for a few minutes immediately after birth while making their way from the birth canal to the maternal pouch. Of these 53 phylotypes, only nine were detected at maternal sites. Overall, the majority of bacteria isolated were novel species (<97 % identity to known 16S rDNA sequences), and each study site (i.e. maternal pouch and saliva, and the GIT of the pouch young) possessed its own unique microbiome.


Subject(s)
Gastrointestinal Tract/microbiology , Macropodidae/microbiology , Metagenome , Saliva/microbiology , Actinobacteria/isolation & purification , Animals , DNA, Bacterial/genetics , Female , Molecular Sequence Data , Phylogeny , Proteobacteria/isolation & purification , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
4.
Vector Borne Zoonotic Dis ; 9(5): 499-503, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19271994

ABSTRACT

A total of 42 ticks comprising Ixodes tasmani (n = 41) and Ixodes trichosuri (n = 1) were collected from wild koalas (Phascolarctos cinereus) at the Koala Convention Centre, Philip Island, Victoria, Australia and screened for the presence of Bartonella using the target gene gltA. Bartonella-like DNA was detected in 4 of the 19 pooled tick samples (21%). All positive ticks were male. Analysis of partial sequences for the gltA gene indicated the presence of a Bartonella-related species similar to that reported in another Ixodid species. This is the first report of Bartonella-like organisms in a native Australian marsupial.


Subject(s)
Bartonella/genetics , DNA, Bacterial/genetics , Ectoparasitic Infestations/veterinary , Ixodes/microbiology , Phascolarctidae , Animals , Ectoparasitic Infestations/epidemiology , Ectoparasitic Infestations/microbiology , Male , Victoria/epidemiology
5.
Vet Immunol Immunopathol ; 129(1-2): 14-27, 2009 May 15.
Article in English | MEDLINE | ID: mdl-19135263

ABSTRACT

In eutherian mammals, CD8 is a key receptor of cytotoxic T cells and plays a pivotal role in the recognition and elimination of infected host cells by cell-mediated cytotoxicity. Here, we report the molecular cloning and expression analysis of CD8alpha and CD8beta cDNAs in two marsupial species, the gray short-tailed opossum and the tammar wallaby. The opossum and tammar CD8 sequences share a high degree of amino acid identity of 63% (CD8alpha) and 57% (CD8beta) to each other as well as 36-45% (CD8alpha) and 38-41% (CD8beta) with their eutherian counterparts. In addition, many of the signature features of eutherian CD8alpha and CD8beta are preserved in both marsupials including the two invariant cysteines that form the intra-chain disulphide bond in the extracellular IgSfV domain and the two hinge region cysteines involved in dimerisation between the two subunits. The p56(lck) binding motif in the cytoplasmic tail of the CD8alpha subunit is also conserved. Interestingly, the opossum CD8alpha and the tammar CD8beta sequences have a truncated cytoplasmic tail. RT-PCR analysis of CD8alpha and CD8beta transcripts in the tissues of the adult opossum and tammar showed broad tissue expression with a high level of expression observed in the lymphoid tissues of both marsupials. Furthermore, RT-PCR analysis of CD8alpha and CD8beta transcripts in the immune tissues of tammar young over the first 120 days of pouch life revealed a pattern of expression analogous to the maturation of the lymphoid tissues. This is the first report confirming the presence of CD8 in the tissues of a marsupial and will provide the tools to further analyse T cell subsets in this unique group of mammals.


Subject(s)
CD8 Antigens/genetics , Macropodidae/immunology , Monodelphis/immunology , Amino Acid Sequence , Animals , Base Sequence , CD8 Antigens/biosynthesis , CD8 Antigens/immunology , Cloning, Molecular , Conserved Sequence , Macropodidae/genetics , Male , Molecular Sequence Data , Monodelphis/genetics , Phylogeny , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction/veterinary , Sequence Alignment
6.
Vet Immunol Immunopathol ; 127(3-4): 269-76, 2009 Feb 15.
Article in English | MEDLINE | ID: mdl-19046773

ABSTRACT

Cathelicidins are important components of the innate immune system and have been identified in skin and epithelia of a range of mammals. In this study molecular techniques, including RACE-PCR, were used to identify the full cDNA sequence of a cathelicidin gene, MaeuCath8, from the Australian marsupial, the tammar wallaby, Macropus eugenii. This cathelicidin was not homologous to other such genes previously isolated from a tammar wallaby mammary gland EST library, however, it did contain 4 conserved cysteine residues which characterise the pre-propeptide and had 80% identity with a previously isolated bandicoot cathelicidin. Reverse transcriptase-PCR established the expression profile of MaeuCath8 in a range of tissues, including spleen, thymus, gastrointestinal tract, skin and liver, of the tammar wallaby from birth to adulthood. Expression of MaeuCath8 was observed in spleen and gastrointestinal tract of newborn animals and was observed in most tissues by 7 days post-partum. The results indicate that pouch young could synthesize their own antimicrobial peptides from an early age suggesting that this ability most likely plays a role in protecting the pouch young from infection prior to the development of immunocompetence.


Subject(s)
Antimicrobial Cationic Peptides/metabolism , Gene Expression Regulation/physiology , Macropodidae/metabolism , Amino Acid Sequence , Animals , Antimicrobial Cationic Peptides/chemistry , Antimicrobial Cationic Peptides/genetics , Base Sequence , Molecular Sequence Data , Phylogeny , Cathelicidins
7.
J Med Entomol ; 45(4): 745-50, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18714878

ABSTRACT

Four species of Rickettsia are recognized as endemic to Australia. This study reports the detection of a new spotted fever group Rickettsia in the common marsupial tick Ixodes tasmani Neumann collected from koalas (Phascolarctos cinereus) in Port Macquarie, NSW, Australia. Based on the results of polymerase chain reaction (PCR) amplification of extracted tick DNA with primers targeting the citrate synthase gene (gltA) and the outer membrane proteins A and B (ompA. ompB), Rickettsiae were detected in 22 of 78 I. tasmani tick samples (28.2%). Sequence data obtained for the three genes displayed the closest degree of similarity to Rickettsia heilongjiangiensiss for gltA (99.4%; 331/333 bp), Rickettsia amblyommii for the ompA gene (94.8%; 417/440 bp), and both Rickettsia massiliae and Rickettsia rhipicephali for the ompB gene (97%; 770/803 bp). BLAST and phylogenetic analysis of partial sequences obtained for the three genes were found to have sufficient nucleotide variation from the current recognized Australian species to be considered a distinct spotted fever group Rickettsia.


Subject(s)
Phascolarctidae/parasitology , Rickettsia rickettsii/isolation & purification , Ticks/microbiology , Animals , Citrate (si)-Synthase/genetics , DNA Primers , DNA, Bacterial/genetics , DNA, Bacterial/isolation & purification , Humans , New South Wales , Phylogeny , Polymerase Chain Reaction , Rickettsia rickettsii/classification , Rickettsia rickettsii/enzymology , Rickettsia rickettsii/genetics
8.
Tissue Cell ; 40(6): 459-66, 2008 Dec.
Article in English | MEDLINE | ID: mdl-18597803

ABSTRACT

Antibodies to the human cathelicidin, hCAP18 have been used to examine epithelial tissues of adult and pouch young marsupials. Immunoreactivity was observed in skin, gastrointestinal tract, lung and mammary node of adults as well as skin, gastrointestinal tract, lung and bone marrow of pouch young. The locations of expression were similar to that reported in human tissues. Although the antibody to hCAP18 is primarily directed at the C-terminal antimicrobial peptide LL37, our observations suggest recognition of a common conserved element of this cathelicidin and lead us to conclude that the epithelial tissues of marsupials are sites of production of cathelicidin. This is consistent with observations in other mammals but is the first report of expression of these compounds in marsupials.


Subject(s)
Antibody Specificity , Antimicrobial Cationic Peptides/immunology , Antimicrobial Cationic Peptides/metabolism , Macropodidae/immunology , Macropodidae/metabolism , Age Factors , Amino Acid Sequence , Animals , Antibodies , Antimicrobial Cationic Peptides/genetics , Epithelium/immunology , Epithelium/metabolism , Epitopes/genetics , Epitopes/immunology , Female , Humans , Immune System/physiology , Immunohistochemistry , Male , Molecular Sequence Data , Species Specificity , Cathelicidins
9.
Appl Environ Microbiol ; 74(17): 5549-55, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18641156

ABSTRACT

The common brushtail possum (Trichosurus vulpecula) is one of the most abundant native marsupials in urban Australia, having successfully adapted to utilize anthropogenic resources. The habituation of possums to food and shelter available in human settlements has facilitated interaction with people, pets, and zoo animals, increasing the potential for transmission of zoonotic Cryptosporidium pathogens. This study sought to examine the identity and prevalence of Cryptosporidium species occurring in possums adapted to urban settings compared to possums inhabiting remote woodlands far from urban areas and to characterize the health of the host in response to oocyst shedding. Findings indicated that both populations were shedding oocysts of the same genotype (brushtail possum 1 [BTP1]) that were genetically and morphologically distinct from zoonotic species and genotypes and most closely related to Cryptosporidium species from marsupials. The urban population was shedding an additional five Cryptosporidium isolates that were genetically distinct from BTP1 and formed a sister clade with Cryptosporidium parvum and Cryptosporidium hominis. Possums that were shedding oocysts showed no evidence of pathogenic changes, including elevated levels of white blood cells, diminished body condition (body mass divided by skeletal body length), or reduced nutritional state, suggesting a stable host-parasite relationship typical of Cryptosporidium species that are adapted to the host. Overall, Cryptosporidium occurred with a higher prevalence in possums from urban habitat (11.3%) than in possums from woodland habitat (5.6%); however, the host-specific nature of the genotypes may limit spillover infection in the urban setting. This study determined that the coexistence of possums with sympatric populations of humans, pets, and zoo animals in the urban Australian environment is unlikely to present a threat to public health safety.


Subject(s)
Cryptosporidiosis/epidemiology , Cryptosporidium/genetics , Trichosurus/parasitology , Analysis of Variance , Animals , Animals, Wild/parasitology , Australia/epidemiology , Cloning, Molecular , Cryptosporidiosis/transmission , Cryptosporidiosis/veterinary , DNA, Protozoan/genetics , Disease Reservoirs/parasitology , Disease Reservoirs/veterinary , Feces/parasitology , Host-Parasite Interactions , Molecular Sequence Data , Oocysts/parasitology , Parasite Egg Count , Phylogeny , Polymerase Chain Reaction , Prevalence , RNA, Ribosomal, 18S/genetics , Sensitivity and Specificity , Sequence Alignment , Species Specificity , Statistics, Nonparametric , Urbanization
10.
Microbiology (Reading) ; 154(Pt 5): 1535-1543, 2008 05.
Article in English | MEDLINE | ID: mdl-18451062

ABSTRACT

The bacterial diversity of the openings of the urogenital and anal tracts of the adult female tammar wallaby, Macropus eugenii, was determined in order to ascertain whether the physical proximity of the openings of these tracts within the cloaca affected the two populations of bacteria. Terminal restriction fragment length polymorphism (T-RFLP) analyses of 42 wallabies identified 81 different terminal fragments, indicative of diverse and complex microbiomes at these anatomical locations. Subsequent amplified rDNA restriction analysis (ARDRA) identified 72 phylotypes from the urogenital tract and 50 from the anal tract. Twenty-two of these phylotypes were common to both tracts. Phylogenetic analysis of sequenced 16S rDNA showed that 83 % of the phylotypes were unidentified species based on the premise that any sequence possessing <97 % homology to a known bacterial species or phylotype was novel. Thus, despite the close proximity of the openings of the urogenital and anal tracts within the cloaca, the two sites retained a diverse range of distinct bacteria, with only a small percentage of overlapping species.


Subject(s)
Cloaca/microbiology , Gastrointestinal Tract/microbiology , Macropodidae/microbiology , Metagenome , Urogenital System/microbiology , Animals , Biodiversity , DNA Fingerprinting , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Female , Molecular Sequence Data , Phylogeny , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
11.
Comp Biochem Physiol B Biochem Mol Biol ; 149(3): 524-33, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18248751

ABSTRACT

Antimicrobial peptides, such as cathelicidin, are an evolutionarily old defense system. However they have more complex actions than just simply their antimicrobial effects, including immunoregulation and interaction with the adaptive immune system. In this study we have characterized several novel cathelicidin-like peptides from the tammar wallaby (Macropus eugenii). The tammar cathelicidin-like (MaeuCath) mRNA were isolated based on the conservation of the cathelin-like amino terminus. Mature MaeuCath peptides were positively charged with hydrophobic carboxyl tails, features that are fundamental for antimicrobial function. MaeuCath1 was induced in tammar leukocytes in response to pathogen-associated molecular patterns from both gram positive and negative bacteria. In addition, we also examined the expression of MaeuCath1 in the primary and secondary lymphoid organs of the tammar neonate throughout early pouch life. The results from this study demonstrate the importance that MaeuCath1 may play in innate defense of the marsupial young, especially in the mucosal organs. Such expression of antimicrobial peptides may form part of the immune strategies of marsupials for neonatal survival during their post-partum development.


Subject(s)
Cathelicidins/metabolism , Macropodidae/metabolism , Amino Acid Sequence , Animals , Cathelicidins/chemistry , Cathelicidins/genetics , Cathelicidins/isolation & purification , Cells, Cultured , Gene Expression Regulation/drug effects , Leukocytes/drug effects , Leukocytes/metabolism , Leukotriene A4/pharmacology , Lipopolysaccharides/pharmacology , Mammary Glands, Animal/drug effects , Mammary Glands, Animal/metabolism , Molecular Sequence Data , Peptides/chemistry , Peptides/genetics , Peptides/isolation & purification , Peptides/metabolism , Phylogeny , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Alignment
12.
Mol Immunol ; 45(3): 690-700, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17706783

ABSTRACT

Two approaches have been used to isolate and identify proteins of the granules of neutrophils of the tammar wallaby, Macropus eugenii. Stimulation with PMA, Ionomycin and calcium resulted in exocytosis of neutrophil granules as demonstrated with electron microscopy. However proteomic analysis using two dimensional gel electrophoresis, in-gel trypsin digestion followed by nano liquid chromatography coupled tandem mass spectrometry (LC-MS/MS) failed to identify any anticipated granule proteins in the reaction supernatants. Subsequent use of differential centrifugation and lysis followed by the application of the same proteomic analysis approach resulted in the isolation and confident identification of 39 proteins, many of which are known to be present in the granules of neutrophils of eutherian mammals or play a role in degranulation. These proteins notably consisted of the known antimicrobials, myeloperoxidase (MPO), serine proteinase, dermcidin, lysozyme and alkaline phosphatase. A number of important known antimicrobials, however, were not detected and these include defensins and cathelicidins. This is the first report of the neutrophil granule proteins of any marsupial and complements previous reports on the cytosolic proteins.


Subject(s)
Anti-Infective Agents/immunology , Cell Degranulation/immunology , Macropodidae/immunology , Neutrophils/immunology , Secretory Vesicles/immunology , Animals , Calcium/pharmacology , Cell Degranulation/drug effects , Ionomycin/pharmacology , Ionophores/pharmacology
13.
Prog Neuropsychopharmacol Biol Psychiatry ; 31(7): 1393-6, 2007 Oct 01.
Article in English | MEDLINE | ID: mdl-17659823

ABSTRACT

Dietary deficiencies in essential omega-3 polyunsaturated fatty acids derived from fish are associated with depression and some fish oils may have therapeutic benefits. We aimed to determine whether taking tuna fish oil confers any additional benefit to conventional outpatient treatment for major depression. A randomized double-blind placebo-controlled four-month trial comparing tuna fish oil versus placebo was conducted on 83 outpatients with major depression. Despite large reductions in depression there were no significant differences at any assessment time point between patients receiving fish oil compared to placebo. Red blood cell incorporation of fatty acids indicated good compliance with oil supplementation, although this sample was not initially deficient in omega-3s. This particular dose and type of fish oil conferred no additional benefit to conventional treatment of depression in this sample. Future studies could target participants with pre-existing omega-3 deficiency and appraise alternate enriched types and higher doses of omega-3 supplementation.


Subject(s)
Depressive Disorder, Major/drug therapy , Fish Oils/therapeutic use , Adolescent , Adult , Aged , Antidepressive Agents/therapeutic use , Depressive Disorder, Major/psychology , Double-Blind Method , Drug Therapy, Combination , Female , Humans , Male , Middle Aged , Psychiatric Status Rating Scales , Treatment Outcome
14.
Mol Immunol ; 44(15): 3641-52, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17521733

ABSTRACT

The gene and corresponding cDNA for CD4 in the gray short-tailed opossum, Monodelphis domestica, and the cDNA sequence for CD4 in the tammar wallaby, Macropus eugenii, have been characterised. The opossum CD4 homolog reveals conserved synteny, preserved genomic organisation and analogous structural arrangement to human and mouse CD4. Opossum and tammar CD4 exhibit typical eutherian CD4 features including the highly conserved p56(lck) binding motif in the cytoplasmic region and the invariant cysteine residues in extracellular domains 1 and 4. Interestingly, the marsupial CD4 sequences substitute a tryptophan for the first cysteine in domain 2 negating the formation of a disulphide bond as seen in other eutherian CD4 sequences except human and mouse. Overall the marsupial CD4 sequences share amino acid identity of 59% to each other and 37-41% with eutherian mammals. However, in contrast to eutherian homologs, the marsupial CD4 sequences were found to be truncated at the terminal end of the cytoplasmic tail. This is the first report confirming the presence of CD4 in a marsupial and describing its key features.


Subject(s)
CD4 Antigens/genetics , Macropodidae/genetics , Monodelphis/genetics , Phylogeny , Amino Acid Sequence , Animals , Base Sequence , CD4 Antigens/chemistry , CD4 Antigens/metabolism , Gene Expression Profiling , Gene Expression Regulation , Genome/genetics , Humans , Molecular Sequence Data , Promoter Regions, Genetic/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Alignment
15.
J Wildl Dis ; 41(3): 611-4, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16244073

ABSTRACT

Serum samples collected from 224 tammar wallabies (Macropus eugenii) in two captive populations in urban areas in eastern New South Wales Australia, between December 1999 and May 2004, were tested for antibodies to Ross River virus (RRV). In one population in northwest Sydney, 21 animals (11%) tested positive, and in another population in Newcastle, New South Wales, thirteen (33%) of the animals were positive. Antibodies were detected in four of 11 wallaroos (Macropus robustus) (36%) but not in parma wallabies (Macropus parma) (n=5), koalas (Phascolarctos cinereus) (n=12) and southern hairy-nosed wombats (Lasiorhinus latifrons) (n=2) from the Sydney area. These data support the possible role of marsupials as urban amplifying hosts for RRV.


Subject(s)
Alphavirus Infections/veterinary , Antibodies, Viral/blood , Marsupialia/virology , Ross River virus/immunology , Alphavirus Infections/epidemiology , Animals , Animals, Zoo , Carrier State/veterinary , Disease Reservoirs/veterinary , Female , Male , New South Wales/epidemiology , Seroepidemiologic Studies
16.
J Anat ; 207(1): 97-102, 2005 Jul.
Article in English | MEDLINE | ID: mdl-16011549

ABSTRACT

Changes in the epithelium of the maternal pouch and the mammary gland of brushtail possums (Trichosurus vulpecula) were examined after animals were treated to induce ovulation with follicle-stimulating hormone (FSH), luteinizing hormone (LH), pregnant mares' serum gonadotrophin (PMSG) and oestradiol. The mammary glands were similar in appearance to those described in eutherian mammals and in previous studies on other marsupials. Exposure of possums to these compounds, particularly PMSG, appeared to result in changes in the mammary glands that could be associated with milk/secretion production. In contrast, the pouch epithelium had a similar histological appearance to that of epithelium from other parts of the body regardless of whether the animal was exposed to stimulants. These preliminary observations are discussed in the context of the purported role of the pouch epithelium and the mammary gland in production of secretions at oestrus and provision of immunological protection to the neonatal marsupial.


Subject(s)
Estrus/physiology , Mammary Glands, Animal/anatomy & histology , Trichosurus/anatomy & histology , Animals , Epithelium/anatomy & histology , Estradiol/pharmacology , Estrus Synchronization , Female , Follicle Stimulating Hormone/pharmacology , Gonadotropins, Equine/pharmacology , Mammary Glands, Animal/physiology , Ovariectomy , Trichosurus/physiology
17.
Dev Comp Immunol ; 28(9): 927-40, 2004 Jul 01.
Article in English | MEDLINE | ID: mdl-15183033

ABSTRACT

This paper describes the cloning of full length marsupial type I interferon (IFN) genes and their flanking regions using a genome walking approach and PCR primers based on previously isolated partial DNA sequences. We confirm that the two major classes of Tammar Wallaby type I IFN genes are homologous with the eutherian IFN-alpha and IFN-beta gene families. The wallaby IFN genes share a number of conserved features with their eutherian counterparts, including codons for cysteines at equivalent positions, implying similar secondary structures for the encoded proteins, and promoter regions with conserved putative regulatory motifs. Moreover, the wallaby genes have AT-rich elements in their flanking sequence corresponding to the mRNA 3'-untranslated regions, also implying that, as in eutherian mammals, rapid mRNA degradation plays a role in regulating expression of these genes. The complex nature of the type I IFN gene families in viviparous mammals (eutherians and marsupials) may reflect their recruitment into nonimmunological processes and this concept is discussed.


Subject(s)
Interferon-alpha/genetics , Interferon-beta/genetics , Macropodidae/genetics , Macropodidae/immunology , Amino Acid Sequence , Animals , Base Sequence , Cloning, Molecular , DNA Primers , Humans , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , Sequence Homology
18.
Immunol Cell Biol ; 82(2): 112-8, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15061761

ABSTRACT

The type I IFN are an important group of multifunctional cytokines that have, for whatever reason, evolved to a high level of complexity in eutherian mammals such as humans and mice. However, until recently, little was known about the type I IFN systems of the other two groups of extant mammals, the marsupials and the egg-laying monotremes. Preliminary partial type I IFN sequences from the short-beaked echidna were previously found to cluster only with the IFN-beta subtype in phylogenetic analyses, but a lack of sequence information made interpretation of these results tenuous. Here, we report cloning of the full-length genes of representatives from the two previously defined groups of echidna type I IFN by genomic walking PCR. Along with analysis of conserved cysteine placement and promoter elements, phylogenetic analysis incorporating these sequences strongly suggest that the two groups of echidna type I IFN genes are in fact homologous to IFN-alpha and IFN-beta, confirming that the duplication leading to these two major classes of type I IFN occurred prior to the divergence of eutherians and monotremes some 180 million years ago. Thus, even though there are major differences in gene copy number and heterogeneity, separate IFN-alpha and IFN-beta gene families are a feature of the cytokine networks of all three groups of living mammals.


Subject(s)
Interferon Type I/genetics , Tachyglossidae/genetics , Amino Acid Sequence , Animals , Cysteine/genetics , Molecular Sequence Data , Phylogeny , Promoter Regions, Genetic , Sequence Alignment , Sequence Analysis, DNA , Sequence Analysis, Protein
19.
Gen Comp Endocrinol ; 133(3): 273-8, 2003 Oct 01.
Article in English | MEDLINE | ID: mdl-12957470

ABSTRACT

Serum cortisol levels were measured in a total of 73 tammar wallabies maintained in a captive population at Macquarie University, NSW, Australia. Previous studies of corticosteroids in marsupials have generally involved low sample numbers, a diverse array of analytical techniques, and a variety of sampling conditions. We have conducted a substantive, longitudinal study of serum cortisol levels using a radioimmunoassay protocol, and data have been analysed with respect to age, sex, and seasonality. There were no apparent effects of age or sex on serum cortisol levels, although an inverse but non-significant relationship was observed between males and females. However a significant difference in serum cortisol levels was observed between seasons, with mean serum cortisol significantly higher in summer than in autumn. These data will serve as a reference for 'normal' ranges of serum cortisol levels, particularly in the female tammar wallaby. As deviations from these values can indicate compromised animal health and well-being, this information will assist wildlife managers in assessing and monitoring the health status of individuals in captive and free-ranging populations.


Subject(s)
Aging/blood , Aging/physiology , Gender Identity , Hydrocortisone/blood , Macropodidae/blood , Macropodidae/physiology , Seasons , Animal Husbandry , Animals , Australia , Female , Longitudinal Studies , Male , Radioimmunoassay
20.
Immunol Lett ; 88(2): 117-25, 2003 Aug 05.
Article in English | MEDLINE | ID: mdl-12880681

ABSTRACT

Although gammadelta T-cells form only a small portion of circulating T-cells in mice and humans, they are more frequent in many other types of mammals and this has lead to speculation regarding their roles and the evolutionary significance of their relative abundance. Moreover, whilst clear homologues of four types of T-cell receptor (TCR) chains (alpha, beta, delta and gamma) have been identified in vertebrates as distantly related as eutherian mammals and cartilaginous fish, there are still many gaps in our knowledge of these TCR components from various taxa. Such knowledge would further illuminate the evolution and function of these receptors and of gammadelta T-cells. Here, we report the molecular cloning of a TCR-delta chain cDNA from the tammar wallaby (Macropus eugenii) which represents the first component of the gammadelta TCR to be characterised from a marsupial. A PCR-based survey of variable (V) segment usage in tammar wallaby mammary-associated lymph node indicated that, although gammadelta T-cells may be sparse in this type of tissue, this species has at least three subfamilies of V genes that have been broadly conserved across vertebrate evolution. Two V subfamilies found in the tammar wallaby were relatively similar and may have diverged more recently, an event that probably occurred at some point in the marsupial lineage.


Subject(s)
Evolution, Molecular , Marsupialia/genetics , Marsupialia/immunology , Receptors, Antigen, T-Cell, gamma-delta/chemistry , Receptors, Antigen, T-Cell, gamma-delta/genetics , Amino Acid Sequence , Animals , Base Sequence , Cloning, Molecular , Conserved Sequence/genetics , Humans , Mice , Molecular Sequence Data , Phylogeny , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid
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