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Featured researches published by Louise Pallant.


Acta Tropica | 1997

Failure of pyrantel in treatment of human hookworm infections (Ancylostoma duodenale) in the Kimberley region of North West Australia

J.A. Reynoldson; Jerzy M. Behnke; Louise Pallant; Marion G. Macnish; Francis Gilbert; S Giles; R.J Spargo; R.C. Andrew Thompson

A survey of 108 individuals from a coastal Aboriginal community in north Western Australia revealed that two species of gastrointestinal protozoan parasites (Giardia duodenalis--39.8%, Entamoeba coli--40.7%) and five gastrointestinal helminths (Hymenolepis nana--54.6%, Hookworm [Ancylostoma duodenale]--30.6%, Enterobius vermicularis--6.5%, Trichuris trichiura--2.8%, Strongyloides stercoralis 1.9%) were present. A total of 29 individuals infected with hookworm were offered treatment with either pyrantel pamoate at a single dose rate of 10 mg/kg body weight or albendazole (single 400 mg dose). Seven days after treatment stool samples were examined. Pyrantel had no significant effect against hookworm. In contrast, albendazole cleared hookworm infections completely and reduced the prevalence of Giardia. The former result suggests that locally A. duodenale is resistant to pyrantel and despite its relatively low cost and wide availability, should not be considered a drug of choice at this dose rate in the treatment of hookworm infections (A. duodenale) in endemic regions.


American Journal of Tropical Medicine and Hygiene | 2012

Soil-transmitted helminthiasis in Laos: A community-wide cross-sectional study of humans and dogs in a mass drug administration environment

James V. Conlan; Boualam Khamlome; Khamphouth Vongxay; Aileen Elliot; Louise Pallant; Banchob Sripa; Stuart D. Blacksell; Stanley G. Fenwick; R.C. Andrew Thompson

We conducted a community cross-sectional survey of soil-transmitted helminthiasis in humans and dogs in four provinces in northern Laos. We collected and tested human and dog fecal samples and analyzed results against sociodemographic data. The prevalence of Ascaris lumbricoides, Trichuris trichiura, hookworm, and Strongyloides stercoralis was 26.1% (95% confidence interval [CI] = 23.7-28.4%), 41.5% (95% CI = 38.8-44.1%), 46.3% (95% CI = 43.3-49.0%), and 8.9% (95% CI = 7.4-10.4%), respectively. We observed strong heterogeneity for helminthiasis by ethnicity, province, and wealth status, which coincided with a risk profile demonstrating that Mon-Khmer persons and the poorest households are highly vulnerable. Necator americanus was the dominant hookworm species infecting humans and Ancylostoma ceylanicum was the only Ancylostoma species detected. Hookworm prevalence in village dogs was 94%, and the dominant species was A. ceylanicum. Necator americanus was also detected in dogs. It appears that dogs have a role in human hookworm transmission and warrant further investigation.


Parasites & Vectors | 2013

Molecular identification of zoonotic and livestock-specific Giardia-species in faecal samples of calves in Southern Germany

Julia Gillhuber; Louise Pallant; Amanda Ash; R.C. Andrew Thompson; Kurt Pfister; Miriam C. Scheuerle

BackgroundGiardia-infection in cattle is often subclinical or asymptomatic, but it can also cause diarrhoea. The livestock-specific species Giardia bovis is the most frequently observed in cattle, however, the two zoonotic species Giardia duodenalis and Giardia enterica have also been found. Therefore calves are thought to be of public health significance. The aim of this study was to obtain current data about the frequency of the different Giardia-species in calves in Southern Germany.FindingsFaecal samples of calves (diarrhoeic and healthy) in Southern Germany, diagnosed Giardia-positive by microscopy, were characterised by multi-locus PCR and sequencing.Of 152 microscopically Giardia-positive samples 110 (72.4%) were positive by PCR and successfully sequenced. G. bovis (Assemblage E) was detected in 101/110 (91.8%) PCR-positive samples, whilst G. duodenalis (Assemblage A) was detected in 8/110 (7.3%) samples and a mixed infection with G. duodenalis and G. bovis (Assemblage A+E) was identified in 1/110 (0.9%) samples. The sub-genotypes A1, E2 and E3 were identified with the β-giardin and the glutamate dehydrogenase genes. In the majority of diarrhoeic faecal samples a co-infection with Cryptosporidium spp. or Eimeria spp. was present, however, there were some in which G. bovis was the only protozoan pathogen found.ConclusionsThe results suggest that there is potentially a risk for animal handlers as calves in Southern Germany are, at a low percentage, infected with the zoonotic species G. duodenalis. In addition, it was found that G. bovis was the only pathogen identified in some samples of diarrhoeic calves, indicating that this parasite may be a contributing factor to diarrhoea in calves.


Veterinary Parasitology | 2013

A high prevalence of Toxoplasma in Australian chickens.

Kamlang Chumpolbanchorn; A.J. Lymbery; Louise Pallant; S. Pan; Yaowalark Sukthana; R.C.A. Thompson

A small survey was undertaken of commercially reared free-range chickens in Western Australia using serology and molecular detection. Eighteen out of 20 serum samples showed antibody responses with titers of 1:64 in 5 chickens and ≥ 1:128 in 13 chickens. DNA extracted from 22 out of 50 tissue samples, 10 brains and 12 spleens, were positive by nested PCR, and sequencing at the B1 locus on DNA from 3 brain and 3 spleen samples confirmed that 2 isolates were Toxoplasma gondii, Type I, and 4 Type II/III. The high prevalence of Toxoplasma infection found in commercial, free-range chickens raises public health issues with respect to both exposure in the workplace, during carcass processing, and subsequent transmission during food handling and/or consumption as food. The results of this study emphasize the need for more data on the incidence of Toxoplasma infection in domestic animals and humans in Australia.


International journal for parasitology. Parasites and wildlife | 2018

Next generation sequencing reveals widespread trypanosome diversity and polyparasitism in marsupials from Western Australia

Crystal Cooper; Sarah Keatley; Amy Northover; Alexander W. Gofton; Frances Brigg; A.J. Lymbery; Louise Pallant; Peta L. Clode; R.C. Andrew Thompson

In Western Australia a number of indigenous Trypanosoma spp. infect susceptible native marsupials, such as the woylie (Bettongia penicillata), brushtail possum (Trichosurus vulpecula), and chuditch (Dasyurus geoffroii). Two genotypes of Trypanosoma copemani (identified as G1 and G2) have been found in the woylie, and G2 has been implicated in the decline of this host species, making its presence of particular interest. Here we used targeted amplicon next generation sequencing (NGS) of the Trypanosoma 18S rDNA loci on 70 Trypanosoma-positive marsupial blood samples, to identify T. copemani genotypes and multiple Trypanosoma infections (polyparasitism) in woylies and cohabiting species in Western Australia. Polyparasitism with Trypanosoma spp. was found in 50% of the wildlife sampled, and within species diversity was high, with 85 zero-radius operational taxonomic units (ZOTUs) identified in nine putative parasite species. Trypanosoma copemani was assigned 17 ZOTUs and was identified in 80% of samples. The most abundant ZOTU isolated (63%) differed slightly from the published genotype of G1, and G2 was the second most abundant ZOTU (14%). Trypanosome diversity was significantly greater in woylies than in brushtail possums, and parasite community composition also differed significantly between these host species. One novel Trypanosoma spp. genotype (Trypanosoma sp. ANU2) was found in 20% of samples. A species of Crithidia was detected in a woylie, and two avian trypanosomes (Trypanosoma avium and Trypanosoma sp. AAT) were identified in woylies for the first time.


Emerging Infectious Diseases | 2016

Rare human infection with pacific broad tapeworm Adenocephalus Pacificus, Australia

Casey V. Moore; R.C. Andrew Thompson; Abdul Jabbar; John V. Williams; Kavita Rasiah; Louise Pallant; Ann P. Koehler; Caitlin R Graham; Gerhard F. Weldhagen

To the Editor: Human diphyllobothriosis associated with the Pacific broad tapeworm Adenocephalus pacificus (syn. Diphyllobothrium pacificum) is a reemerging, global parasitic disease (1). Infection with the adult tapeworm occurs widely in piscivorous mammals, including humans, with various species of marine fish acting as intermediate hosts (1,2). In the Southern Hemisphere, the organism is well described in the coastal waters of South America, southern Africa, and Oceania (2). A. pacificus tapeworms have been recorded in pinnipeds in Australian territory as far back as 1923 (3). To our knowledge, no human case has been reported from this region to date.


Pallant, L. <http://researchrepository.murdoch.edu.au/view/author/Pallant, Louise.html>, MacDonald, L.M. <http://researchrepository.murdoch.edu.au/view/author/MacDonald, Louisa.html>, Sargent, K. <http://researchrepository.murdoch.edu.au/view/author/Sargent, Keith.html>, Armson, A. <http://researchrepository.murdoch.edu.au/view/author/Armson, Anthony.html>, Reynoldson, J. <http://researchrepository.murdoch.edu.au/view/author/Reynoldson, James.html> and Thompson, R.C.A. <http://researchrepository.murdoch.edu.au/view/author/Thompson, Andrew.html> (2003) The application of quantitative-PCR for high throughput screening of novel compounds against cryptosporidium parvum In Vitro and their subsequent IC50. In: Thompson, R.C.A., (ed.) Cryptosporidium: From Molecules to Disease. Elsevier B.V., Amsterdam, The Netherlands, pp. 413-416. | 2003

The application of quantitative-PCR for high throughput screening of novel compounds against cryptosporidium parvum In Vitro and their subsequent IC50

Louise Pallant; L.M. MacDonald; K. Sargent; A. Armson; J.A. Reynoldson; Andrew Thompson

A quantitative-PCR (Q-PCR) method that uses an in vitro culturing system for Cryptosporidium parvum has been developed. This sensitive method allows standardization of an in vitro culturing system and its development for quantitative assessment using PCR. This chapter presents a study in which this system was assessed against an established counting method which is widely used to enumerate parasites, particularly following exposure to anti-parasitic compounds. There are several sources of variability inherent in, in vitro culturing systems which could result in an inaccurate final amount of DNA being detected per culture well. These can be summarized as cumulative effects because of variability in the in vitro system and the DNA extraction and quantification method. Analysis of the variability in this in vitro culturing system using Q-PCR indicates that it is a consistent and reliable system which offers higher sensitivity and specificity when compared with counting methods as well as providing a vast improvement in sample.


Cryptosporidium#R##N#From Molecules to Disease | 2003

An Examination of the Activity of the Dinitroanilines on Cryptosporidium Parvum Using In Vitro, In Vivo and Target Expression Methods

A. Armson; R.C.A. Thompson; K. Mennon; L.M. MacDonald; A.J. O'Hara; K. Sargent; Louise Pallant; J.A. Reynoldson

More than 200 compounds have been tested for activity against Cryptosporidium parvum, both in vitro and in vivo, there is still no effective treatment. Previous studies have revealed the anticryptosporidial effect of the tubulin specific herbicides, the dinitroanilines. The in vitro activities of two members of this class of compounds, oryzalin and trifluralin have been demonstrated against Cryptosporidium. Recent studies exposed IC50 values for oryzalin and trifluralin against Cryptosporidium of 750 and 800 nM, respectively. This chapter presents a study, the aim of which on-going study is to examine tubulin as an effective target both in vivo and ex vivo.


Journal of Clinical Microbiology | 1998

Comparison of PCR and Microscopy for Detection of Cryptosporidium parvum in Human Fecal Specimens: Clinical Trial

U.M. Morgan; Louise Pallant; B.W. Dwyer; David Forbes; G. Rich; R.C.A. Thompson


Parasites & Vectors | 2015

The epidemiology of infections with Giardia species and genotypes in well cared for dogs and cats in Germany

Louise Pallant; Dieter Barutzki; Roland Schaper; R.C.A. Thompson

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Abdul Jabbar

University of Melbourne

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Casey V. Moore

Institute of Medical and Veterinary Science

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Crystal Cooper

University of Western Australia

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