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1.
Behav Res Ther ; 144: 103926, 2021 09.
Article in English | MEDLINE | ID: mdl-34242837

ABSTRACT

Trait worry is a hallmark feature of anxiety and depression, interfering with attentional control and impairing cognitive performance. Previous research has shown the adaptive dual n-back training is effective in improving attentional control and reducing emotional vulnerability, but not for everyone. The current randomised controlled trial explored the role of baseline emotional vulnerability and perceived cognitive impact in training-related cognitive and emotional improvements in 60 high worriers randomly assigned to 10 sessions of the adaptive dual n-back training or non-adaptive 1-back training. Pre-training, post-training and one-month follow-up measures of cognitive performance were assessed using an emotional Flanker task, a cued task-switching task, and the MaRs-IB task. Self-report questionnaires assessed worry, anxiety, depression, somatisation, and self-efficacy, as well as participants' perceived cognitive impact of the training. Participants with higher levels of baseline emotional vulnerability presented the largest improvements in non-verbal reasoning and emotional vulnerability one month after the training, as well as the greatest perceived cognitive impact. Perceived cognitive impact was predicted by working memory improvement on the adaptive n-back training at high baseline levels of anxiety. These results suggest that the adaptive n-back training presents the greatest emotional and cognitive benefits for individuals experiencing severe levels of emotional vulnerability.


Subject(s)
Anxiety , Memory, Short-Term , Affect , Anxiety/therapy , Anxiety Disorders , Cognition , Humans
2.
Mol Biochem Parasitol ; 180(1): 56-61, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21840345

ABSTRACT

Angiostrongylus vasorum is an emerging parasite of dogs and related carnivores throughout western Europe and presents a biosecurity threat to many countries worldwide. Infections are difficult to diagnose due to a high variability of clinical signs and can be fatal if left untreated. Previous attempts to develop indirect ELISA as a diagnostic test for antibody presence in dogs have been limited by cross-reactive recognition of antibodies to other endemic nematodes. This study compared the immuno-dominant soluble somatic proteins for first stage, third stage and adult A. vasorum using Western blotting. 2D electrophoresis and mass spectrometry were further used to identify specific immuno-dominant proteins (n=14) within the soluble fraction from whole adult worms. Proteins included an aspartyl protease inhibitor, representing a potential candidate for a recombinant-based ELISA and novel vaccine.


Subject(s)
Angiostrongylus/chemistry , Angiostrongylus/immunology , Antigens, Helminth/chemistry , Dog Diseases/parasitology , Helminth Proteins/chemistry , Mass Spectrometry/methods , Strongylida Infections/veterinary , Angiostrongylus/genetics , Angiostrongylus/growth & development , Animals , Antigens, Helminth/genetics , Antigens, Helminth/immunology , Blotting, Western , Dogs , Helminth Proteins/genetics , Helminth Proteins/immunology , Molecular Sequence Data , Strongylida Infections/parasitology
3.
Parasitol Res ; 109(6): 1577-83, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21537986

ABSTRACT

This study reports the development of a real-time PCR assay and an indirect ELISA to improve on current detection of canine Angiostrongylus vasorum infection. A highly specific fluorescent probe-based, real-time PCR assay was developed to target the A. vasorum second internal transcribed spacer region and detected DNA in EDTA blood, lung tissue, broncho-alveolar larvage fluid, endotracheal mucus, pharyngeal swabs and faecal samples. PCR was fast (∼1 h), highly efficient when using EDTA blood samples, consistently detected a single molecule of parasite DNA and did not amplify DNA from other parasitic nematodes or definitive host species. An indirect ELISA was also developed using the soluble protein fraction from adult A. vasorum worms. Some cross-reactive antigen recognition was observed when tested against sera from dogs infected with Crenosoma vulpis (n = 8), Toxocara canis (n = 5) and Dirofilaria immitis (n = 5). This was largely overcome by setting the cut-off for a positive result at an appropriately high level. Field evaluation of the real-time PCR and ELISA was conducted by testing sera and EDTA blood from dogs with suspected A. vasorum infection (n = 148) and compared with the Baermann's larval migration test in faeces. Thirty-one dogs were positive by at least one test. Of these, 20 (65%) were detected by the Baermann method, 18 (58%) by blood PCR, 24 (77%) by ELISA and 28 (90%) by blood PCR and ELISA together. Combined testing using real-time PCR and ELISA therefore improved the detection rate of A. vasorum infection and holds promise for improved clinical diagnosis and epidemiological investigation.


Subject(s)
Angiostrongylus/isolation & purification , DNA, Protozoan/blood , Enzyme-Linked Immunosorbent Assay/veterinary , Real-Time Polymerase Chain Reaction/veterinary , Strongylida Infections/diagnosis , Angiostrongylus/genetics , Animals , DNA Primers , Dog Diseases/parasitology , Dogs , RNA, Ribosomal, 18S/genetics , RNA, Ribosomal, 28S , RNA, Ribosomal, 5.8S/genetics , Sensitivity and Specificity , Strongylida Infections/epidemiology , Strongylida Infections/veterinary
4.
Vet Parasitol ; 173(3-4): 344-8, 2010 Oct 29.
Article in English | MEDLINE | ID: mdl-20674179

ABSTRACT

Multiple species of metastrongylid lungworm (Nematoda: Metastrongyloidea) have been reported to infect members of the Felidae. This study describes two metastrongylid species infecting cats in Ibiza, Spain, including clinical features of infection and diagnosis via morphological and molecular characterisation of larval stages. Cats (n=7) presented with suspect lungworm infection, exhibiting coughing and other respiratory signs of infection. Faecal samples were collected from each cat and were subjected to the Baermann method for the detection of first stage larvae. In four cats, two different species of larvae were observed on the basis of morphology and were further molecularly characterised by PCR and sequencing of the 18S rRNA gene. Sequence data confirmed the presence of Aelurostrongylus abstrusus and an unknown species of Troglostrongylus. Molecular characterisation of Oslerus rostratus is also reported for the first time. Given the diversity of metastrongylid species capable of infecting cats, and morphological similarity of larval stages, an emphasis should be placed on the use of molecular characterisation for accurate diagnosis of infection.


Subject(s)
Cat Diseases/parasitology , Metastrongyloidea/isolation & purification , Phylogeny , Strongylida Infections/veterinary , Animals , Base Sequence , Cats , DNA, Helminth/chemistry , DNA, Helminth/genetics , Feces/parasitology , Larva/ultrastructure , Mediterranean Islands , Metastrongyloidea/genetics , Metastrongyloidea/ultrastructure , Molecular Sequence Data , Parasite Egg Count/veterinary , Polymerase Chain Reaction/veterinary , RNA, Ribosomal, 18S/chemistry , RNA, Ribosomal, 18S/genetics , Sequence Alignment , Sequence Analysis, DNA , Strongylida Infections/parasitology
5.
Vet Parasitol ; 172(3-4): 299-304, 2010 Sep 20.
Article in English | MEDLINE | ID: mdl-20570049

ABSTRACT

Metastrongyloid induced pneumonia has been described sporadically in the red panda (Ailurus fulgens). Early descriptions in pandas recently imported to the USA from China involved parasites morphologically similar to Angiostrongylus spp. and Crenosomatidae. More recently, four cases of severe verminous pneumonia associated with Angiostrongylus vasorum have been reported from European zoos. A coprological survey of the red panda population within European zoos was conducted in 2008. Faecal samples from 115 pandas originating from 54 zoos were collected on 3 consecutive days. Using Baermann technique, 40 animals (35%) from 20 zoos (37%) were found to shed metastrongyloid first stage larvae (L(1)). Based on their morphology and size, the L(1) observed could be divided into three morphologically distinct types: (1) a Crenosoma sp. type (n=5, overall prevalence: 4.3%), (2) an A. vasorum type (n=3, 2.6%), and (3) an unidentified metastrongyloid species, similar to, but morphologically distinct from A. vasorum (n=32, 27.8%). Further confirmation of species identification was provided by PCR amplification and sequencing of the 18S rRNA gene, which confirmed three different species. The novel Crenosoma species was most genetically analogous to Crenosoma mephitidis and the unidentified metastrongyloid species was most similar to Stenurus minor and Torynurus convulutus. Routine and quarantine health care of red pandas in captivity should take account of the risk of Angiostrongylus and Crenosoma infection in endemic areas, but should also be cognisant of the widespread presence of an apparently less pathogenic species of lungworm. The identity of the two potentially novel species is subject to further work.


Subject(s)
Ailuridae/parasitology , Animals, Zoo/parasitology , Biodiversity , Helminthiasis, Animal/epidemiology , Metastrongyloidea/physiology , Nematode Infections/veterinary , Animals , Europe , Feces/parasitology , Female , Larva/anatomy & histology , Male , Metastrongyloidea/anatomy & histology , Metastrongyloidea/classification , Metastrongyloidea/genetics , Molecular Sequence Data , Nematode Infections/epidemiology , Prevalence , RNA, Ribosomal, 18S/genetics
6.
Parasitol Int ; 58(4): 406-10, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19683596

ABSTRACT

The geographic range of Angiostrongylus vasorum is expanding, leading to increased disease. Although observed cases of canine pulmonary angiostrongylosis have been dutifully reported in the literature, the state of biological knowledge remains too poor to predict future patterns of spread with any confidence. Nevertheless, there is an urgent need to identify areas that are likely to be suitable for parasite establishment. Preliminary attempts to do this using a climatic envelope approach suggest that several new areas are open to colonisation, even without invoking climate change. The risk of parasite importation into these areas should be mitigated, e.g. by restricting movement of dogs unless tested or treated for A. vasorum, and monitored by focused surveillance of definitive and intermediate hosts. These efforts will benefit from newly developed diagnostic tests.


Subject(s)
Angiostrongylus/physiology , Climate Change , Dog Diseases/epidemiology , Lung Diseases, Parasitic/veterinary , Strongylida Infections/veterinary , Angiostrongylus/classification , Angiostrongylus/isolation & purification , Animals , Dog Diseases/parasitology , Dog Diseases/transmission , Dogs , Host-Parasite Interactions , Lung Diseases, Parasitic/epidemiology , Lung Diseases, Parasitic/parasitology , Lung Diseases, Parasitic/transmission , Strongylida Infections/epidemiology , Strongylida Infections/parasitology , Strongylida Infections/transmission
7.
J Eukaryot Microbiol ; 56(3): 290-5, 2009.
Article in English | MEDLINE | ID: mdl-19527357

ABSTRACT

The morphology and genetic characterisation of a new species of piroplasm identified in the blood of the Gilbert's potoroo (Potorous gilbertii) from the Two Peoples Bay Nature Reserve near Albany, Western Australia, is described from blood and tissue samples from 16 Gilbert's potoroos. Microscopy of blood showed these parasites are highly pleomorphic with a mean length of 1.8 mum and mean width of 0.85 mum. Phylogenetic analysis of 18S rRNA sequence data identified the piroplasm as a new species of Theileria that is closely related to other Australian marsupial piroplasm species. Based on biological and molecular data, it is proposed that the parasite from Gilbert's potoroo be given the name Theileria gilberti n. sp.


Subject(s)
Potoroidae/parasitology , Theileria/classification , Theileria/isolation & purification , Animals , Blood/parasitology , Cluster Analysis , DNA, Protozoan/chemistry , DNA, Protozoan/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Genes, rRNA , Microscopy/methods , Molecular Sequence Data , Phylogeny , RNA, Protozoan/genetics , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA , Theileria/cytology , Western Australia
8.
J Vet Diagn Invest ; 21(2): 270-3, 2009 Mar.
Article in English | MEDLINE | ID: mdl-19286513

ABSTRACT

A 9-year-old, male, captive red panda (Ailurus fulgens fulgens) in an urban zoo in the United Kingdom presented with respiratory distress and weight loss. The animal was euthanatized, and a postmortem examination was performed. The lungs were diffusely consolidated with extensive mineralization. Microscopically, there was extensive obliteration of normal pulmonary architecture by sheets and coalescing nodules of partially mineralized fibrous tissue and granulomatous inflammation centered on large numbers of nematode larvae and eggs. First stage nematode larvae were isolated from lung tissue and were characterized as Angiostrongylus vasorum on the basis of their morphology and sequencing of the 18S ribosomal RNA gene and the entire second internal transcribed spacer. Although A. vasorum has previously been reported in red pandas in a zoological collection in Denmark, this study is the first reported case in the United Kingdom and occurs against a background of geographical spread and increased incidence of disease in domestic and wild canids. Angiostrongylus vasorum should be considered a differential diagnosis for respiratory disease in the red panda and taken into account when planning parasite and pest control programs for zoological collections.


Subject(s)
Ailuridae/parasitology , Angiostrongylus/growth & development , Pneumonia/veterinary , Strongylida Infections/veterinary , Angiostrongylus/genetics , Animals , Base Sequence , Fatal Outcome , Male , Molecular Sequence Data , Pneumonia/parasitology , Pneumonia/pathology , Polymerase Chain Reaction , Strongylida Infections/parasitology , Strongylida Infections/pathology
9.
Exp Parasitol ; 119(2): 301-3, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18367174

ABSTRACT

This study analysed the intracellular delivery capacity of insect derived pyrrhocoricin with a peptide cargo in Cryptosporidium parvum in vitro using fluorescence microscopy. Results revealed that pyrrhocoricin was capable of acting as a delivery vehicle in transducing peptides across the parasite cell membrane for multiple life-cycle stages. The successful transduction may aid in target validation and the delivery of future peptide-based drugs against this important human pathogen.


Subject(s)
Antimicrobial Cationic Peptides , Antiprotozoal Agents/administration & dosage , Cryptosporidium parvum/metabolism , Drug Carriers , Insect Proteins , Peptides/administration & dosage , Animals , Fluorescein/chemistry , Microscopy, Fluorescence
10.
Exp Parasitol ; 118(3): 303-7, 2008 Mar.
Article in English | MEDLINE | ID: mdl-17945214

ABSTRACT

The present study was undertaken to analyse the capability of HIV-1 derived TAT protein transduction domain (PTD) fused with Green Fluorescent Protein (TAT-GFP) as a delivery vehicle into a range of protozoan parasites. Successful transduction of native purified TAT-GFP was observed by fluorescent microscopy in Cryptosporidium parvum, Giardia duodenalis, and Neospora caninum. The ability to transduce peptides and other cargo into protozoan parasites, will greatly assist in the delivery of future peptide-based drugs and target validation peptides.


Subject(s)
Cryptosporidium parvum/metabolism , Drug Delivery Systems/methods , Giardia/metabolism , Neospora/metabolism , Toxoplasma/metabolism , tat Gene Products, Human Immunodeficiency Virus/physiology , Animals , Cats , Green Fluorescent Proteins/physiology , Image Processing, Computer-Assisted , Mice , Microscopy, Fluorescence
12.
J Parasitol ; 89(2): 409-12, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12760669

ABSTRACT

The haemoprotozoan Babesia canis has been recognized in Australia for many years, and a second, smaller species has recently been discovered. Amplification and sequencing of a partial region of the 18S small subunit ribosomal RNA (rRNA) gene enabled detection and characterization of the large and small canine babesiae of Australia for the first time. Isolates from northern Australia were genetically characterized to be 99% homologous to Babesia canis vogeli, confirming previous speculation about the subspecies of B. canis endemic to Australia. The partial 18S rRNA gene sequence amplified from isolates obtained in southeastern Australia was genetically identical to Babesia gibsoni, a species not previously known in Australia. The polymerase chain reaction (PCR) used was shown to be specific to Babesia and had a high sensitivity, detecting DNA at a parasitemia of approximately 0.0000027%. This study also reports the first known detection and characterization of B. canis DNA in Rhipicephalus sanguineus ticks using PCR.


Subject(s)
Babesia/isolation & purification , Babesiosis/veterinary , Dog Diseases/parasitology , Polymerase Chain Reaction/veterinary , Animals , Arachnid Vectors/parasitology , Australia , Babesia/classification , Babesia/genetics , Babesiosis/diagnosis , Babesiosis/parasitology , Base Sequence , DNA, Protozoan/blood , DNA, Protozoan/chemistry , DNA, Ribosomal/blood , DNA, Ribosomal/chemistry , Dog Diseases/diagnosis , Dogs , Erythrocytes/parasitology , Ixodidae/parasitology , Molecular Sequence Data , Parasitemia/diagnosis , Parasitemia/parasitology , Parasitemia/veterinary , RNA, Protozoan/genetics , RNA, Ribosomal, 18S/genetics , Sensitivity and Specificity , Sequence Alignment/veterinary , Sequence Homology, Nucleic Acid
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