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1.
Dev Genes Evol ; 211(1): 10-9, 2001 Jan.
Article in English | MEDLINE | ID: mdl-11277400

ABSTRACT

We have cloned a Hox-like gene, cnox-2Am, from a staghorn coral, Acropora millepora, an anthozoan cnidarian, and characterised its embryonic and larval expression. cnox-2Am and its orthologs in other cnidarians and Trichoplax most closely resemble the Gsx and, to a lesser extent, Hox 3/4 proteins. Developmental northern blots and in situ hybridisation are consistent in showing that cnox-2Am message appears in the planula larva shortly after the oral/aboral axis is formed following gastrulation. Expression is localised in scattered ectodermal cells with a restricted distribution along the oral/aboral body axis. They are most abundant along the sides of the cylindrical larva, rare in the oral region and absent from the aboral region. These cells, which on morphological grounds we believe to be neurons, are of two types; one tri-or multipolar near the basement membrane and a second extending projections in both directions from a mid-ectodermal nucleus. Anti-RFamide staining reveals neurons with a similar morphology to the cnox-2Am-expressing cells. However, RFamide-expressing neurons are more abundant, especially at the aboral end of the planula, where there is no cnox-2Am expression. The pattern of expression of cnox-2Am resembles that of Gsx orthologs in Drosophila and vertebrates in being expressed in a spatially restricted portion of the nervous system.


Subject(s)
Cnidaria/genetics , Genes, Homeobox , Homeodomain Proteins/genetics , Homeodomain Proteins/metabolism , Protozoan Proteins , Amino Acid Sequence , Animals , Blotting, Northern , Cnidaria/cytology , Cnidaria/embryology , Cnidaria/metabolism , Embryo, Nonmammalian/cytology , Embryo, Nonmammalian/metabolism , Embryonic Development , Gene Expression Regulation, Developmental , Homeodomain Proteins/chemistry , Immunohistochemistry , In Situ Hybridization , Larva/genetics , Larva/metabolism , Molecular Sequence Data , Neurons/cytology , Neurons/metabolism , Neuropeptides/metabolism , Phylogeny , Protein Structure, Tertiary , Sequence Alignment
2.
Proc Natl Acad Sci U S A ; 97(9): 4475-80, 2000 Apr 25.
Article in English | MEDLINE | ID: mdl-10781047

ABSTRACT

Pax genes encode a family of transcription factors, many of which play key roles in animal embryonic development but whose evolutionary relationships and ancestral functions are unclear. To address these issues, we are characterizing the Pax gene complement of the coral Acropora millepora, an anthozoan cnidarian. As the simplest animals at the tissue level of organization, cnidarians occupy a key position in animal evolution, and the Anthozoa are the basal class within this diverse phylum. We have identified four Pax genes in Acropora: two (Pax-Aam and Pax-Bam) are orthologs of genes identified in other cnidarians; the others (Pax-Cam and Pax-Dam) are unique to Acropora. Pax-Aam may be orthologous with Drosophila Pox neuro, and Pax-Bam clearly belongs to the Pax-2/5/8 class. The Pax-Bam Paired domain binds specifically and preferentially to Pax-2/5/8 binding sites. The recently identified Acropora gene Pax-Dam belongs to the Pax-3/7 class. Clearly, substantial diversification of the Pax family occurred before the Cnidaria/higher Metazoa split. The fourth Acropora Pax gene, Pax-Cam, may correspond to the ancestral vertebrate Pax gene and most closely resembles Pax-6. The expression pattern of Pax-Cam, in putative neurons, is consistent with an ancestral role of the Pax family in neural differentiation and patterning. We have determined the genomic structure of each Acropora Pax gene and show that some splice sites are shared both between the coral genes and between these and Pax genes in triploblastic metazoans. Together, these data support the monophyly of the Pax family and indicate ancient origins of several introns.


Subject(s)
Cnidaria/classification , Cnidaria/genetics , Evolution, Molecular , Genetic Variation , Multigene Family , Phylogeny , Transcription Factors/genetics , Amino Acid Sequence , Animals , Cnidaria/embryology , Consensus Sequence , Drosophila/genetics , Embryo, Nonmammalian , Female , Male , Molecular Sequence Data , Ovum/chemistry , RNA Splicing , RNA, Messenger/genetics , Sequence Alignment , Sequence Homology, Amino Acid , Spermatozoa/chemistry , Transcription Factors/chemistry
3.
Vaccine ; 17(1): 31-9, 1999 Jan.
Article in English | MEDLINE | ID: mdl-10078605

ABSTRACT

Cellular and humoral immune responses of mice to Onchocerca volvulus glutathione S-transferase (OvGST) presented via in vivo expression in attenuated Salmonella typhimurium were examined and compared with the same antigen administered by subcutaneous injection with Freund's adjuvant. After infection with recombinant S. typhimurium, maximal numbers of bacteria were recovered from the mesenteric lymph nodes and spleens during the second week postinfection. By weeks 3-4, bacteria were absent from these tissues. Splenocytes from mice infected with S. typhimurium expressing OvGST showed significant and specific proliferative responses to OvGST, whereas the non-recombinant S. typhimurium controls and those which received the antigen by subcutaneous injection with Freund's adjuvant did not. Mice infected with recombinant S. typhimurium had elevated IFN-gamma levels over non-recombinant S. typhimurium and placebo controls. but IL-4 and IL-5 levels were low and did not differ significantly between these groups. Antibody responses to OvGST antigen expressed by a recombinant Salmonella vaccine or delivered in a purified form with Freund's adjuvant were moderate to high. These data suggest that Salmonella can be used as a vaccine delivery vector that induces specific cellular and humoral immune responses to Onchocerca volvulus antigens. This is the first report to describe the successful application of a filarial antigen in a live-vector delivery system as well as the first recombinant based filarial vaccine to elicit a cellular immune response similar to that described for putative immune endemics.


Subject(s)
Glutathione Transferase/immunology , Onchocerca volvulus/enzymology , Onchocerca volvulus/immunology , Onchocerciasis/prevention & control , Salmonella typhimurium/enzymology , Salmonella typhimurium/immunology , Vaccines, Synthetic/immunology , Administration, Oral , Animals , Antibodies, Bacterial/biosynthesis , Antibodies, Helminth/biosynthesis , Antibody Formation/drug effects , Antibody Formation/immunology , Cytokines/biosynthesis , Epitopes, T-Lymphocyte/biosynthesis , Epitopes, T-Lymphocyte/immunology , Female , Freund's Adjuvant/pharmacology , Glutathione Transferase/biosynthesis , Glutathione Transferase/genetics , Immunity, Cellular/immunology , Immunoblotting , Lymph Nodes/immunology , Lymph Nodes/microbiology , Lymphocyte Activation/immunology , Mice , Mice, Inbred BALB C , Onchocerca volvulus/genetics , Onchocerciasis/immunology , Salmonella typhimurium/genetics , Spleen/immunology , Spleen/metabolism , Spleen/microbiology , T-Lymphocytes/immunology , Vaccines, Attenuated/immunology , Vaccines, Attenuated/therapeutic use , Vaccines, Synthetic/therapeutic use
4.
Emerg Infect Dis ; 4(4): 641-4, 1998.
Article in English | MEDLINE | ID: mdl-9866742

ABSTRACT

In a recent case of scrub typhus in Australia, Orientia tsutsugamushi isolated from the patient's blood was tested by sequence analysis of the 16S rDNA gene. The sequence showed a strain of O. tsutsugamushi that was quite different from the classic Karp, Kato, and Gilliam strains. The new strain has been designated Litchfield.


Subject(s)
Orientia tsutsugamushi/classification , Adult , Animals , Australia , DNA, Ribosomal/analysis , Female , Humans , Male , Mice , Orientia tsutsugamushi/genetics , RNA, Ribosomal, 16S/analysis , Scrub Typhus/microbiology
5.
Dev Genes Evol ; 208(6): 352-6, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9716726

ABSTRACT

Vertebrate Pax-6 and its Drosophila homolog eyeless play central roles in eye specification, although it is not clear if this represents the ancestral role of this gene class. As the most "primitive" animals with true nervous systems, the Cnidaria may be informative in terms of the evolution of the Pax gene family. For this reason we surveyed the Pax gene complement of a representative of the basal cnidarian class (the Anthozoa), the coral Acropora millepora. cDNAs encoding two coral Pax proteins were isolated. Pax-Aam encoded a protein containing only a paired domain, whereas Pax-Cam also contained a homeodomain clearly related to those in the Pax-6 family. The paired domains in both proteins most resembled the vertebrate Pax-2/5/8 class, but shared several distinctive substitutions. As in most Pax-6 homologs and orthologs, an intron was present in the Pax-Cam locus at a position corresponding to residues 46/47 in the homeodomain. We propose a model for evolution of the Pax family, in which the ancestor of all of the vertebrate Pax genes most resembled Pax-6, and arose via fusion of a Pax-Aam-like gene (encoding only a paired domain) with an anteriorly-expressed homeobox gene resembling the paired-like class.


Subject(s)
Cnidaria/genetics , DNA-Binding Proteins/genetics , Eye Proteins/genetics , Homeodomain Proteins , Amino Acid Sequence , Animals , DNA, Complementary , Molecular Sequence Data , PAX6 Transcription Factor , Paired Box Transcription Factors , Repressor Proteins , Sequence Homology, Amino Acid
6.
Biochim Biophys Acta ; 1282(2): 179-81, 1996 Jul 25.
Article in English | MEDLINE | ID: mdl-8703971

ABSTRACT

cDNA clones from the parasitic nematodes Onchocerca volvulus and Onchocerca gibsoni encode homologs of the yeast proteins MRS3 and MRS4. Together with an uncharacterised ORF on chromosome III of Caenorhabditis elegans, these constitute a new class of proteins belonging to the mitochondrial solute carrier protein superfamily. So far, five other members of this protein family have been identified in C. elegans, but levels of identity between these and the Onchocerca proteins were considerably lower. Consideration of cysteine content and overall charge implies that the natural substrates of the nematode proteins are small ions.


Subject(s)
Carrier Proteins/genetics , Cation Transport Proteins , DNA, Complementary/chemistry , Fungal Proteins/genetics , Onchocerca/genetics , Repressor Proteins , Saccharomyces cerevisiae Proteins , Adenosine Diphosphate/metabolism , Adenosine Triphosphate/metabolism , Amino Acid Sequence , Animals , Carrier Proteins/chemistry , Cell Membrane/chemistry , Cysteine/analysis , Cytosol/chemistry , Fungal Proteins/chemistry , Mitochondrial Proteins , Molecular Sequence Data , Sequence Alignment
7.
Mol Biochem Parasitol ; 63(1): 49-57, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8183322

ABSTRACT

A novel repetitive antigen from the cattle parasite Onchocerca gibsoni was shown to be recognised by sera from humans infected with Onchocerca volvulus, Wuchereria bancroftii or Brugia malayi. The O. gibsoni protein was produced in a recombinant form, and antibodies raised to this protein used to screen cDNA libraries for O. volvulus. A series of clones were isolated which encoded repetitive regions very similar to those in O. gibsoni, but interspersed between these were longer repeating units which we have not so far found in O. gibsoni. The repetitive antigen was shown to be of high molecular weight and present only in the insoluble (membrane) fraction of O. gibsoni microfilariae. Immunofluorescence techniques demonstrated that the antigen was associated both with muscle and with specific membrane layers, including a peripheral layer which corresponds to either the outer hypodermis or an inner region of the cuticle in adult female O. gibsoni. In many respects, the proteins encoded by the O. gibsoni and O. volvulus cDNA clones resembled repetitive antigens from several distantly related eukaryotic parasites, and a possible common role in immune evasion is discussed.


Subject(s)
Antigens, Helminth/isolation & purification , Onchocerca/immunology , Amino Acid Sequence , Animals , Antibodies, Helminth/blood , Antigens, Helminth/genetics , Antigens, Helminth/metabolism , Brugia malayi/immunology , Cross Reactions , DNA, Complementary/genetics , Elephantiasis, Filarial/immunology , Female , Filariasis/immunology , Helminth Proteins/genetics , Helminth Proteins/immunology , Humans , Immunohistochemistry , Male , Microfilariae/genetics , Microfilariae/immunology , Molecular Sequence Data , Onchocerca/genetics , Onchocerca volvulus/genetics , Onchocerca volvulus/immunology , Onchocerciasis/immunology , Onchocerciasis/parasitology , Recombinant Proteins/genetics , Recombinant Proteins/immunology , Repetitive Sequences, Nucleic Acid , Sequence Homology, Amino Acid , Wuchereria bancrofti/immunology
8.
Int J Parasitol ; 22(5): 685-7, 1992 Aug.
Article in English | MEDLINE | ID: mdl-1399255

ABSTRACT

mRNA from uterine microfilariae of the cattle parasite Onchocerca gibsoni was used for the construction of cDNA libraries. A cDNA clone encoding an antigen recognized by serum from human individuals infected with O. volvulus was found to contain five copies of an 87 bp unit. These 87 bp units were present in the genome in high copy number as long tandem arrays. These are the first cDNA sequence data obtained directly from larvae of any Onchocerca species.


Subject(s)
Antigens, Helminth/genetics , DNA/chemistry , Onchocerca/genetics , Amino Acid Sequence , Animals , Base Sequence , Cattle , Female , Humans , Microfilariae/genetics , Microfilariae/immunology , Molecular Sequence Data , Onchocerca/immunology , Uterus/parasitology
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