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1.
Acta Parasitol ; 60(3): 451-8, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26204182

ABSTRACT

Henneguya leporinicola is a parasite of the gill filament of Leporinus macrocephalus, a characiform fish belonging to the Anostomidae family, which is of major economic importance. Despite the damage it causes in fish, little is known about this parasite. Therefore, a study was undertaken with fourteen specimens of L. macrocephalus taken from fish farms in the state of Sao Paulo. The fish were collected and examined searching for lesions and/or myxosporean plasmodia. One of the specimens (7.14%) contained white elongated plasmodia in the gill filament. The mature spores had elongated bodies with polar capsules of equal size and a caudal length greater than body length. Morphological characteristics identified the parasite as H. leporinicola. Molecular analysis of the 18S rDNA sequence resulted in a 1954 bp, demonstrating significant genetic differences with previously described species of Henneguya/Myxobolus. Phylogenetic analysis comparing the 18S rDNA sequence of H. leporinicola with other species, previously described in South America, and the 20 closest species as indicated by BLASTn Max Score showed H. leporinicola as a basal branch of a subclade composed by Henneguya spp. parasite of characiform hosts.


Subject(s)
Characiformes/parasitology , Fish Diseases/parasitology , Myxozoa/classification , Myxozoa/isolation & purification , Parasitic Diseases, Animal/parasitology , Animals , Aquaculture , Brazil , Cluster Analysis , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Fish Diseases/pathology , Gills/parasitology , Gills/pathology , Histocytochemistry , Microscopy , Molecular Sequence Data , Myxozoa/cytology , Myxozoa/genetics , Parasitic Diseases, Animal/pathology , Phylogeny , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA
2.
Dis Aquat Organ ; 107(2): 129-39, 2013 Dec 12.
Article in English | MEDLINE | ID: mdl-24334355

ABSTRACT

Henneguya piaractus and Myxobolus colossomatis (Myxosporea: Myxobolidae) are commonly found in the characid Piaractus mesopotamicus, an important fish farm species in Brazil. This paper describes the prevalence, mean intensity, molecular phylogeny, ultrastructure, and histology of H. piaractus and M. cf. colossomatis found infecting specimens of P. mesopotamicus collected from fish farms in the state of São Paulo, Brazil. A total of 278 fish were collected from 3 fish farms between February 2008 and July 2010. Parasite prevalence and mean intensity varied throughout the study period, and according to location and year. A phylogenetic tree, placing South American species in a global context, showed a clear tendency among myxosporean species to cluster according to host families. Ultrastructural analysis for M. cf. colossomatis showed the plasmodial wall with numerous projections toward host cells and phagocytic activity. Histopathological data showed hyperplasia caused by H. piaractus in highly infected fish. Histological and ultrastructural analysis of H. piaractus showed results similar to those that have previously been reported.


Subject(s)
Characiformes , Fish Diseases/parasitology , Myxozoa/genetics , Parasitic Diseases, Animal/parasitology , Animals , Brazil/epidemiology , Fish Diseases/pathology , Gills/pathology , Gills/ultrastructure , Myxozoa/classification , Parasitic Diseases, Animal/epidemiology , Phylogeny , Prevalence
3.
Immunogenetics ; 63(5): 319-24, 2011 May.
Article in English | MEDLINE | ID: mdl-21301827

ABSTRACT

Bovines present contrasting, heritable phenotypes of infestations with the cattle tick, Rhipicephalus (Boophilus) microplus. Tick salivary glands produce IgG-binding proteins (IGBPs) as a mechanism for escaping from host antibodies that these ectoparasites ingest during blood meals. Allotypes that occur in the constant region of IgG may differ in their capacity to bind with tick IGBPs; this may be reflected by the distribution of distinct allotypes according to phenotypes of tick infestations. In order to test this hypothesis, we investigated the frequency of haplotypes of bovine IgG2 among tick-resistant and tick-susceptible breeds of bovines. Sequencing of the gene coding for the heavy chain of IgG2 from 114 tick-resistant (Bos taurus indicus, Nelore breed) and tick-susceptible (B. t. taurus, Holstein breed) bovines revealed SNPs that generated 13 different haplotypes, of which 11 were novel and 5 were exclusive of Holstein and 3 of Nelore breeds. Alignment and modeling of coded haplotypes for hinge regions of the bovine IgG2 showed that they differ in the distribution of polar and hydrophobic amino acids and in shape according to the distribution of these amino acids. We also found that there was an association between genotypes of the constant region of the IgG2 heavy chain with phenotypes of tick infestations. These findings open the possibility of investigating if certain IgG allotypes hinder the function of tick IGBPs. If so, they may be markers for breeding for resistance against tick infestations.


Subject(s)
Cattle Diseases/genetics , Cattle/genetics , Genetic Predisposition to Disease , Immunoglobulin Heavy Chains/genetics , Immunoglobulin gamma-Chains/genetics , Tick Infestations/veterinary , Amino Acid Sequence , Animals , Base Sequence , Cattle/immunology , Cattle Diseases/immunology , Cattle Diseases/parasitology , Haplotypes , Male , Molecular Sequence Data , Polymorphism, Single Nucleotide , Salivary Glands/immunology , Tick Infestations/genetics , Tick Infestations/immunology , Ticks/immunology
4.
Acta Trop ; 100(3): 192-8, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17141165

ABSTRACT

In order to evaluate the potential use of TS14 antigen in an enzyme-linked immunosorbent assay (ELISA) for immunodiagnosis of neurocysticercosis (NC), its open reading frame (ORF) was amplified by RT-PCR from mRNA isolated from Taenia solium cysticerci. The ORF was subcloned into the expression vector pET-28a, and was used to transform Escherichia coli BL21 (DE3) cells to produce TS14 antigen. The His-tagged expressed protein was purified on a nickel affinity column. Using the HISTS14 as antigen, ELISA was positive for 100% of cerebrospinal fluid (CSF) and 97% of serum samples from NC patients. No positive results were observed with sera and CSF samples from control groups. Cross-reactivity with sera from patients with schistosomiasis and Chagas' disease was not observed. Serum samples from patients with taeniasis were evaluated and 2 of 13 cases showed reactivity in this assay. Our data indicate the usefulness of HISTS14 in ELISA for an accurate and rapid assay for diagnosis of NC and seroepidemiological studies.


Subject(s)
Antibodies, Helminth/blood , Antibodies, Helminth/cerebrospinal fluid , Helminth Proteins/metabolism , Neurocysticercosis/diagnosis , Taenia solium/immunology , Animals , Antibodies, Helminth/immunology , Antigens, Helminth/immunology , Enzyme-Linked Immunosorbent Assay/methods , Escherichia coli/metabolism , Helminth Proteins/chemistry , Helminth Proteins/immunology , Humans , Molecular Weight , Neurocysticercosis/blood , Neurocysticercosis/cerebrospinal fluid , Recombinant Proteins/biosynthesis , Recombinant Proteins/immunology , Sensitivity and Specificity , Serologic Tests/methods , Species Specificity
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