<?xml version = '1.0' encoding = 'UTF-8'?>
<?xml-stylesheet href="/rss/styledrssBMC.css" type="text/css"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:extra="http://www.biomedcentral.com/xml/schemas/extra/" xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:cc="http://web.resource.org/cc/">
	<channel rdf:about="http://www.biomedcentral.com/rss">
		<extra:info rdf:parseType="Literal">
			<html:div xmlns:html="http://www.w3.org/1999/xhtml" style="font:14px Verdana, Geneva, Arial, Helvetica, sans-serif">
				<html:span style="font-weight:bold">This is an RSS newsfeed from BioMed Central</html:span>
				<html:br/>
				<html:span style="font-size: 12px;">It is intended to be used with an RSS reader. For more information about RSS newsfeeds from BioMed Central, visit <html:br/><html:a href="http://www.biomedcentral.com/info/about/rss/" style="color:#3333CC; font-size:12px;">http://www.biomedcentral.com/info/about/rss/</html:a><html:br/>
				</html:span>
			</html:div>
		</extra:info>
		<title>Parasites &amp; Vectors - Most viewed articles</title>
		<link>http://www.parasitesandvectors.commostviewed/</link>
		<description>Most viewed articles in last 30 days from Parasites &amp; Vectors (ISSN 1756-3305) published by 
				
				BioMed Central
		</description>
        <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
         <items>
            <rdf:Seq>
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/21"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/20"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/19"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/10"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/18"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/22"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/15"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/16"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/13"/>			    
            
				    <rdf:li rdf:resource="http://www.parasitesandvectors.com/content/1/1/17"/>			    
            
            </rdf:Seq>
        </items>
    </channel>
    
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/21">
            
            <title>A monoclonal antibody marker for the exclusion-zone filaments of Trypanosoma brucei</title>
			<description>Background:
Trypanosoma brucei is a haemoflagellate pathogen of man, wild animals and domesticated livestock in central and southern Africa. In all life cycle stages this parasite has a single mitochondrion that contains a uniquely organised genome that is condensed into a flat disk-like structure called the kinetoplast. The kinetoplast is essential for insect form procyclic cells and therefore is a potential drug target. The kinetoplast is unique in nature because it consists of novel structural proteins and thousands of circular, interlocking, DNA molecules (kDNA). Secondly, kDNA replication is critically timed to coincide with nuclear S phase and new flagellum biogenesis. Thirdly, the kinetoplast is physically attached to the flagellum basal bodies via a structure called the tripartite attachment complex (TAC). The TAC consists of unilateral filaments (within the mitochondrion matrix), differentiated mitochondrial membranes and exclusion-zone filaments that extend from the distal end of the basal bodies. To date only one protein, p166, has been identified to be a component of the TAC.
Results:
In the work presented here we provide data based on a novel EM technique developed to label and characterise cytoskeleton structures in permeabilised cells without extraction of mitochondrion membranes. We use this protocol to provide data on a new monoclonal antibody reagent (Mab 22) and illustrate the precise localisation of basal body-mitochondrial linker proteins. Mab 22 binds to these linker proteins (exclusion-zone filaments) and provides a new tool for the characterisation of cytoskeleton mediated kinetoplast segregation.
Conclusion:
The antigen(s) recognised by Mab 22 are cytoskeletal, insensitive to extraction by high concentrations of non-ionic detergent, extend from the proximal region of basal bodies and bind to the outer mitochondrial membrane. This protein(s) is the first component of the TAC exclusion-zone fibres to be identified. Mab 22 will therefore be important in characterising TAC biogenesis.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/21</link>		
			<dc:creator>M&#233;lanie Bonhivers, Nicolas Landrein, Marion Decossas and Derrick R Robinson</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:21</dc:source>
			<dc:subject>Number of accesses: 312</dc:subject>
			<dc:date>2008-07-10</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-21</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>21</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-10</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/20">
            
            <title>Different serological cross-reactivity of Trypanosoma rangeli forms in Trypanosoma cruzi-infected patients sera</title>
			<description>Background:
American Trypanosomiasis or Chagas disease is caused by Trypanosoma cruzi which currently infects approximately 16 million people in the Americas causing high morbidity and mortality. Diagnosis of American trypanosomiasis relies on serology, primarily using indirect immunofluorescence assay (IFA) with T. cruzi epimastigote forms. The closely related but nonpathogenic Trypanosoma rangeli has a sympatric distribution with T. cruzi and is carried by the same vectors. As a result false positives are frequently generated. This confounding factor leads to increased diagnostic test costs and where false positives are not caught, endangers human health due to the toxicity of the drugs used to treat Chagas disease.
Results:
In the present study, serologic cross-reactivity between the two species was compared for the currently used epimastigote form and the more pathologically relevant trypomastigote form, using IFA and immunoblotting (IB) assays. Our results reveal an important decrease in cross reactivity when T. rangeli culture-derived trypomastigotes are used in IFA based diagnosis of Chagas disease. Western blot results using sera from both acute and chronic chagasic patients presenting with cardiac, indeterminate or digestive disease revealed similar, but not identical, antigenic profiles.
Conclusion:
This is the first study addressing the serological cross-reactivity between distinct forms and strains of T. rangeli and T. cruzi using sera from distinct phases of the Chagasic infection. Several T. rangeli-specific proteins were detected, which may have potential as diagnostic tools.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/20</link>		
			<dc:creator>Milene H de Moraes, Alessandra A Guarneri, Fabiana P Girardi, Juliana B Rodrigues, Iriane Eger, Kevin M Tyler, M&#225;rio Steindel and Edmundo C Grisard</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:20</dc:source>
			<dc:subject>Number of accesses: 304</dc:subject>
			<dc:date>2008-07-08</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-20</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>20</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-08</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/19">
            
            <title>A 15N stable isotope semen label to detect mating in the malaria mosquito Anopheles arabiensis Patton</title>
			<description>In previous studies it was determined that the stable isotope 13-carbon can be used as a semen label to detect mating events in the malaria mosquito Anopheles arabiensis. In this paper we describe the use of an additional stable isotope, 15-nitrogen (15N), for that same purpose. Both stable isotopes can be analysed simultaneously in a mass spectrometer, offering the possibility to detect both labels in one sample in order to study complex and difficult-to-detect mating events, such as multiple mating. 15N-glycine was added to larval rearing water and the target enrichment was 5 atom% 15N. Males from these trays were mated with unlabelled virgin females, and spiked spermathecae were analysed for isotopic composition after mating using mass spectrometry. Results showed that spermathecae positive for semen could be distinguished from uninseminated or control samples using the raw delta15Nper thousand values. The label persisted in spermathecae for up to 5 days after insemination, and males aged 10 days transferred similar amounts of label as males aged 4 days. There were no negative effects of the label on larval survival and male longevity. Enrichment of teneral mosquitoes after emergence was 4.85 +/- 0.10 atom% 15N. A threshold value defined as 3 standard deviations above the mean of virgin (i.e. uninseminated spermathecae) samples was successful in classifying a large proportion of samples correctly (i.e. on average 95%). We conclude that alongside 13C, 15N can be used to detect mating in Anopheles and the suitability of both labels is briefly discussed.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/19</link>		
			<dc:creator>Michelle EH Helinski, Rebecca C Hood, Doris Gludovacz, Leo Mayr and Bart GJ Knols</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:19</dc:source>
			<dc:subject>Number of accesses: 287</dc:subject>
			<dc:date>2008-07-01</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-19</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>19</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-01</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/10">
            
            <title>Canine leishmaniasis in Southern Italy: a role for nitric oxide released from activated macrophages in asymptomatic infection?</title>
			<description>Background:
Human and canine leishmaniasis (CanL) by Leishmania infantum is endemic in Italy, with a high percentage of infected asymptomatic animals. However, the immune response mechanisms underlying the clinical presentation of CanL have not been fully investigated. Among leishmanicidal molecules produced by activated macrophages, nitric oxide (NO) produced by an inducible NO synthase seems to play an important protective role, but no conclusive data are available. Therefore, NO released by cultured macrophages from dogs with natural Leishmania infection living in an endemic area for CanL was evaluated.
Methods:
On the basis of one year's clinical and laboratory follow-up, 22 dogs infected by Leishmania infantum were identified and grouped as: asymptomatic dogs (n = 13) and dogs with symptoms of leishmaniasis (n = 9). Each animal was bled twice at 4-month intervals and macrophage and lymphocyte cultures were obtained from peripheral blood mononuclear cells. Supernatants of L. infantum-infected macrophage cultures, with or without addition of autologous lymphocytes, were assayed for NO production by Griess reaction for nitrites.
Results:
In the first months of the infection the levels of NO in supernatants of Leishmania-infected macrophages were higher in symptomatic than in asymptomatic dogs, but they were significantly increased in the latter group eight months after the diagnosis of infection. Furthermore, NO release significantly decreased in the presence of autologous lymphocytes in both groups of animals.
Conclusion:
These results suggest that NO may be involved in the long-term protection of dogs against natural Leishmania infection and in the clinical presentation of canine leishmaniasis in the Mediterranean area.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/10</link>		
			<dc:creator>Maria A Panaro, Olga Brandonisio, Donato de Caprariis, Pasqua Cavallo, Antonia Cianciulli, Vincenzo Mitolo and Domenico Otranto</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:10</dc:source>
			<dc:subject>Number of accesses: 236</dc:subject>
			<dc:date>2008-05-09</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-10</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>10</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-09</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/18">
            
            <title>UMF-078: A modified flubendazole with potent macrofilaricidal activity against Onchocerca ochengi in African cattle</title>
			<description>Background:
Human onchocerciasis or river blindness, caused by the filarial nematode Onchocerca volvulus, is currently controlled using the microfilaricidal drug, ivermectin. However, ivermectin does not kill adult O. volvulus, and in areas with less than 65% ivermectin coverage of the population, there is no effect on transmission. Therefore, there is still a need for a macrofilaricidal drug. Using the bovine filarial nematode O. ochengi (found naturally in African cattle), the macrofilaricidal efficacy of the modified flubendazole, UMF-078, was investigated.
Methods:
Groups of 3 cows were treated with one of the following regimens: (a) a single dose of UMF-078 at 150 mg/kg intramuscularly (im), (b) 50 mg/kg im, (c) 150 mg/kg intraabomasally (ia), (d) 50 mg/kg ia, or (e) not treated (controls).
Results:
After treatment at 150 mg/kg im, nodule diameter, worm motility and worm viability (as measured by metabolic reduction of tetrazolium to formazan) declined significantly compared with pre-treatment values and concurrent controls. There was abrogation of embryogenesis and death of all adult worms by 24 weeks post-treatment (pt). Animals treated at 50 mg/kg im showed a decline in nodule diameter together with abrogated reproduction, reduced motility, and lower metabolic activity in isolated worms, culminating in approximately 50% worm mortality by 52 weeks pt. Worms removed from animals treated ia were not killed, but exhibited a temporary embryotoxic effect which had waned by 12 weeks pt in the 50 mg/kg ia group and by 24 weeks pt in the 150 mg/kg ia group. These differences could be explained by the different absorption rates and elimination half-lives for each dose and route of administration.
Conclusion:
Although we did not observe any signs of mammalian toxicity in this trial with a single dose, other studies have raised concerns regarding neuro- and genotoxicity. Consequently, further evaluation of this compound has been suspended. Nonetheless, these results validate the molecular target of the benzimidazoles as a promising lead for rational design of macrofilaricidal drugs.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/18</link>		
			<dc:creator>Barend M deC Bronsvoort, Benjamin L Makepeace, Alfons Renz, Vincent N Tanya, Lawrence Fleckenstein, David Ekale and Alexander J Trees</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:18</dc:source>
			<dc:subject>Number of accesses: 222</dc:subject>
			<dc:date>2008-06-20</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-18</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>18</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-20</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/22">
            
            <title> Lutzomyia adiketis sp. n. (Diptera: Phlebotomidae), a vector of Paleoleishmania neotropicum sp. n. (Kinetoplastida: Trypanosomatidae) in Dominican amber </title>
			<description>Background:
Amber can be used to trace the history of disease-vector associations because microorganisms are preserved "in situ" inside the alimentary tract and body cavity of blood-sucking insects.
Results:
Lutzomyia adiketis sp. nov. (Phlebotomidae: Diptera) is described from Dominican amber as a vector of Paleoleishmania neotropicum sp. nov. (Kinetoplastida: Trypanosomatidae),  The fossil sand fly species differs from all previously described extinct and extant members of the genus by the following combination of characters: Sc forked with the branches meeting the costa and radius veins; wing L/W value of 4.1; a  delta  value of 18, a ratio beta/alpha value of 0.86 and the shape and size of the spatulate rods on the ninth sternite.  The trypanosomatid is characterized by the nature of the promastigotes, amastigotes and paramastigotes and by being carried by an extinct species of sand fly.
Conclusions:
Morphological characters show that the fossil sand fly is a new extinct species and that it was host to a digenetic species of trypanosomatid.  This study provides the first fossil evidence that Neotropical sand flies were vectors of trypanosomatids in the mid-Tertiary.   </description>
			<link>http://www.parasitesandvectors.com/content/1/1/22</link>		
			<dc:creator>George Poinar</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:22</dc:source>
			<dc:subject>Number of accesses: 222</dc:subject>
			<dc:date>2008-07-15</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-22</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>22</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-07-15</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/15">
            
            <title>Molecular characterization of freshwater snails in the genus Bulinus: a role for barcodes?</title>
			<description>Background:
Reliable and consistent methods are required for the identification and classification of freshwater snails belonging to the genus Bulinus (Gastropoda, Planorbidae) which act as intermediate hosts for schistosomes of both medical and veterinary importance. The current project worked towards two main objectives, the development of a cost effective, simple screening method for the routine identification of Bulinus isolates and the use of resultant sequencing data to produce a model of relationships within the group.
Results:
Phylogenetic analysis of the DNA sequence for a large section (1009 bp) of the mitochondrial gene cytochrome oxidase subunit 1 (cox1) for isolates of Bulinus demonstrated superior resolution over that employing the second internal transcribed spacer (its2) of the ribosomal gene complex. Removal of transitional substitutions within cox1 because of saturation effects still allowed identification of snails at species group level. Within groups, some species could be identified with ease but there were regions where the high degree of molecular diversity meant that clear identification of species was problematic, this was particularly so within the B. africanus group.
Conclusion:
The sequence diversity within cox1 is such that a barcoding approach may offer the best method for characterization of populations and species within the genus from different geographical locations. The study has confirmed the definition of some accepted species within the species groups but additionally has revealed some unrecognized isolates which underlines the need to use molecular markers in addition to more traditional methods of identification. A barcoding approach based on part of the cox1 gene as defined by the Folmer primers is proposed.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/15</link>		
			<dc:creator>Richard A Kane, J Russell Stothard, Aidan M Emery and David Rollinson</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:15</dc:source>
			<dc:subject>Number of accesses: 219</dc:subject>
			<dc:date>2008-06-10</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-15</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>15</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-10</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/16">
            
            <title>Lutzomyia longipalpis s.l. in Brazil and the impact of the Sao Francisco River in the speciation of this sand fly vector</title>
			<description>Lutzomyia longipalpis s.l. (Diptera: Psychodidae) is the principal vector of Leishmania infantum chagasi in the Americas, and constitutes a complex of species. Various studies have suggested an incipient speciation process based on behavioral isolation driven by the chemotype of male sexual pheromones. It is well known that natural barriers, such as mountains and rivers can directly influence population divergence in several organisms, including insects. In this work we investigated the potential role played by the Sao Francisco River in eastern Brazil in defining the current distribution of Lu. longipalpis s.l. Our studies were based on analyses of polymorphisms of the cytochrome b gene (cyt b) sequences from Lu. longipalpis s.l. available in public databases, and from additional field-caught individuals. Altogether, 9 distinct populations and 89 haplotypes were represented in the analyses. Lu. longipalpis s.l. populations were grouped according to their distribution in regards to the 10&#176;S parallel: north of 10&#176;S (&lt;10&#176;S); and south of 10&#176;S (>10&#176;S). Our results suggest that although no polymorphisms were fixed, moderate genetic divergences were observed between the groups analyzed (i.e., FST = 0.184; and Nm = 2.22), and were mostly driven by genetic drift. The population divergence time estimated between the sand fly groups was about 0.45 million years (MY), coinciding with the time of the change in the course of the Sao Francisco River, during the Mindel glaciation. Overall, the polymorphisms on the cyt b haplotypes and the current speciation process detected in Lu. longipalpis s.l. with regards to the distribution of male sexual pheromones suggest a role of the Sao Francisco River as a significant geographical barrier in this process.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/16</link>		
			<dc:creator>Iliano V Coutinho-Abreu, Ivan V Sonoda, Jose A Fonseca, Marcia A Melo, Valdir Q Balbino and Marcelo Ramalho-Ortig&#227;o</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:16</dc:source>
			<dc:subject>Number of accesses: 202</dc:subject>
			<dc:date>2008-06-12</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-16</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>16</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-12</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/13">
            
            <title>Nature limits filarial transmission</title>
			<description>Lymphatic filariasis, caused by Wuchereria bancrofti, Brugia malayi and B. timori is a public health problem of considerable magnitude of the tropics and subtropics. Presently 1.3 billion people are at risk of lymphatic filariasis (LF) infection and about 120 million people are affected in 83 countries. In this context it is worth mentioning that 'nature' itself limits filarial transmission to a great extent in a number of ways such as by reducing vector populations, parasitic load and many other bearings. Possibilities to utilize these bearings of natural control of filariasis should be searched and if manipulations on nature, like indiscriminate urbanization and deforestation, creating sites favourable for the breeding of filarial vectors and unsanitary conditions, water pollution with organic matters etc., are reduced below the threshold level, we will be highly benefited. Understandings of the factors related to natural phenomena of control of filariasis narrated in this article may help to adopt effective control strategies.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/13</link>		
			<dc:creator>Goutam Chandra</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:13</dc:source>
			<dc:subject>Number of accesses: 190</dc:subject>
			<dc:date>2008-05-23</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-13</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>13</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-23</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.parasitesandvectors.com/content/1/1/17">
            
            <title>Loss of protection with insecticide-treated nets against pyrethroid-resistant Culex quinquefasciatus mosquitoes once nets become holed: an experimental hut study</title>
			<description>Background:
An important advantage of pyrethroid-treated nets over untreated nets is that once nets become worn or holed a pyrethroid treatment will normally restore protection. The capacity of pyrethroids to kill or irritate any mosquito that comes into contact with the net and prevent penetration of holes or feeding through the sides are the main reasons why treated nets continue to provide protection despite their condition deteriorating over time. Pyrethroid resistance is a growing problem among Anopheline and Culicine mosquitoes in many parts of Africa. When mosquitoes become resistant the capacity of treated nets to provide protection might be diminished, particularly when holed. An experimental hut trial against pyrethroid-resistant Culex quinquefasciatus was therefore undertaken in southern Benin using a series of intact and holed nets, both untreated and treated, to assess any loss of protection as nets deteriorate with use and time.
Results:
There was loss of protection when untreated nets became holed; the proportion of mosquitoes blood feeding increased from 36.2% when nets were intact to between 59.7% and 68.5% when nets were holed to differing extents. The proportion of mosquitoes blood feeding when treated nets were intact was 29.4% which increased to 43.6&#8211;57.4% when nets were holed. The greater the number of holes the greater the loss of protection regardless of whether nets were untreated or treated. Mosquito mortality in huts with untreated nets was 12.9&#8211;13.6%; treatment induced mortality was less than 12%. The exiting rate of mosquitoes into the verandas was higher in huts with intact nets.
Conclusion:
As nets deteriorate with use and become increasingly holed the capacity of pyrethroid treatments to restore protection is greatly diminished against resistant Culex quinquefasciatus mosquitoes.</description>
			<link>http://www.parasitesandvectors.com/content/1/1/17</link>		
			<dc:creator>SR Irish, R N'Guessan, PM Boko, C Metonnou, A Odjo, M Akogbeto and M Rowland</dc:creator>
			<dc:source>Parasites &amp; Vectors 2008, 1:17</dc:source>
			<dc:subject>Number of accesses: 189</dc:subject>
			<dc:date>2008-06-18</dc:date>
			<dc:identifier>doi:10.1186/1756-3305-1-17</dc:identifier>
			
			
							
					<prism:publicationName>Parasites &amp; Vectors</prism:publicationName>
					
			
							
					<prism:issn>1756-3305</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>17</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-06-18</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
		
	<cc:License rdf:about="http://creativecommons.org/licenses/by/2.0/">
         <cc:permits rdf:resource="http://creativecommons.org/ns#Reproduction"/>
         <cc:permits rdf:resource="http://creativecommons.org/ns#Distribution"/>
         <cc:permits rdf:resource="http://creativecommons.org/ns#DerivativeWorks"/>
	</cc:License>
</rdf:RDF>
