scholarly journals Ankyrin-1 gene exhibits allelic heterogeneity in conferring protection against malaria

2017 ◽  
Author(s):  
Hong Ming Huang ◽  
Denis C. Bauer ◽  
Patrick M. Lelliott ◽  
Matthew W. A. Dixon ◽  
Leann Tilley ◽  
...  
Keyword(s):  
Direct Evidence ◽  
Allelic Heterogeneity ◽  
Plasmodium Chabaudi ◽  
Gene Encoding ◽  
Mutagenesis Screen ◽  
Future Studies ◽  
Host Parasite Interactions ◽  
Malaria Susceptibility ◽  
Erythrocyte Clearance ◽  
Host Parasite

AbstractAllelic heterogeneity is a common phenomenon where a gene exhibit different phenotype depending on the nature of its genetic mutations. In the context of genes affecting malaria susceptibility, it allowed us to explore and understand the intricate host-parasite interactions during malaria infections. In this study, we described a gene encoding erythrocytic ankyrin-1 (Ank-1) which exhibits allelic-dependent heterogeneous phenotypes during malaria infections. We conducted an ENU mutagenesis screen on mice and identified twoAnk-1mutations, one resulted in an amino acid substitution (MRI95845), and the other a truncatedAnk-1protein (MRI96570). Both mutations caused hereditary spherocytosis-like phenotypes and confer differing protection againstPlasmodium chabaudiinfections. Upon further examination, theAnk-1(MRI96570)mutation was found to inhibit intra-erythrocytic parasite maturation, whereasAnk-1(MW95845)caused increased bystander erythrocyte clearance during infection. This is the first description of allelic heterogeneity in ankyrin-1 from the direct comparison between twoAnk-1mutations. Despite the lack of direct evidence from population studies, this data further supported the protective roles of ankyrin-1 mutations in conferring malaria protection. This study also emphasized the importance of such phenomenon to achieve a better understanding of host-parasite interactions, which could be the basis of future studies.

scholarly journals The Ponto-Caspian parasite Plagioporus cf. skrjabini reaches the River Rhine system in Central Europe: higher infestation in the native than in the introduced Danubian form of the gastropod Theodoxus fluviatilis

Hydrobiologia ◽  
2021 ◽  
Author(s):  
Louisa Marie Rothmeier ◽  
René Sahm ◽  
Burkard Watermann ◽  
Karsten Grabow ◽  
Meike Koester ◽  
...  
Keyword(s):  
Freshwater Snail ◽  
Trematode Species ◽  
River Rhine ◽  
Future Studies ◽  
Northern European ◽  
Host Parasite Interactions ◽  
Theodoxus Fluviatilis ◽  
Native Populations ◽  
Host Parasite ◽  
European Form

AbstractThe introduction of non-indigenous organisms in new areas in the context of host-parasite interactions is still poorly understood. This study aimed at a parasitological and histopathological comparison of two phylogenetically distinct forms of the freshwater snail Theodoxus fluviatilis in the River Rhine system: the native Northern-European form, which showed a decline for unknown reasons and is nowadays extinct in the River Rhine, and the non-indigenous Danubian form, which was introduced via the Main–Danube canal. We histopathologically examined populations of Northern-European T. fluviatilis from three smaller rivers of the Rhine system and of Danubian T. fluviatilis from the River Rhine, after confirming the phylogenetic background of the respective population genetically. Results showed differences in the prevalence of trematodes and histopathologic organic alterations between the two snail forms. Both were infected with an opecoelid trematode Plagioporus cf. skrjabini, whereby its prevalence was significantly higher in the Northern-European than in the Danubian form. The parasitic trematode is, to our knowledge, a new trematode species in the River Rhine system, presumably co-introduced through the invasion of its second intermediate and final hosts, i.e. Ponto-Caspian amphipods and gobies. Its impact on native populations of Northern-European T. fluviatilis needs to be subject of future studies.

Host parasite interactions and pathophysiology in Giardia infections

2011 ◽  
Vol 41 (9) ◽  
pp. 925-933 ◽  
Author(s):  
James A. Cotton ◽  
Jennifer K. Beatty ◽  
Andre G. Buret
Keyword(s):  
Host Parasite Interactions ◽  
Host Parasite

scholarly journals Spatial expression pattern of serine proteases in the blood fluke Schistosoma mansoni determined by fluorescence RNA in situ hybridization

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Lenka Ulrychová ◽  
Pavel Ostašov ◽  
Marta Chanová ◽  
Michael Mareš ◽  
Martin Horn ◽  
...  
Keyword(s):  
In Situ Hybridization ◽  
Schistosoma Mansoni ◽  
Rna Sequencing ◽  
Serine Proteases ◽  
Expression Patterns ◽  
High Sensitivity ◽  
Host Parasite Interactions ◽  
Highly Sensitive ◽  
Host Parasite

Abstract Background The blood flukes of genus Schistosoma are the causative agent of schistosomiasis, a parasitic disease that infects more than 200 million people worldwide. Proteases of schistosomes are involved in critical steps of host–parasite interactions and are promising therapeutic targets. We recently identified and characterized a group of S1 family Schistosoma mansoni serine proteases, including SmSP1 to SmSP5. Expression levels of some SmSPs in S. mansoni are low, and by standard genome sequencing technologies they are marginally detectable at the method threshold levels. Here, we report their spatial gene expression patterns in adult S. mansoni by the high-sensitivity localization assay. Methodology Highly sensitive fluorescence in situ RNA hybridization (FISH) was modified and used for the localization of mRNAs encoding individual SmSP proteases (including low-expressed SmSPs) in tissues of adult worms. High sensitivity was obtained due to specifically prepared tissue and probes in combination with the employment of a signal amplification approach. The assay method was validated by detecting the expression patterns of a set of relevant reference genes including SmCB1, SmPOP, SmTSP-2, and Sm29 with localization formerly determined by other techniques. Results FISH analysis revealed interesting expression patterns of SmSPs distributed in multiple tissues of S. mansoni adults. The expression patterns of individual SmSPs were distinct but in part overlapping and were consistent with existing transcriptome sequencing data. The exception were genes with significantly low expression, which were also localized in tissues where they had not previously been detected by RNA sequencing methods. In general, SmSPs were found in various tissues including reproductive organs, parenchymal cells, esophagus, and the tegumental surface. Conclusions The FISH-based assay provided spatial information about the expression of five SmSPs in adult S. mansoni females and males. This highly sensitive method allowed visualization of low-abundantly expressed genes that are below the detection limits of standard in situ hybridization or by RNA sequencing. Thus, this technical approach turned out to be suitable for sensitive localization studies and may also be applicable for other trematodes. The results suggest that SmSPs may play roles in diverse processes of the parasite. Certain SmSPs expressed at the surface may be involved in host–parasite interactions. Graphic abstract

scholarly journals Urogenital Schistosomiasis—History, Pathogenesis, and Bladder Cancer

2021 ◽  
Vol 10 (2) ◽  
pp. 205
Author(s):  
Lúcio Lara Santos ◽  
Júlio Santos ◽  
Maria João Gouveia ◽  
Carina Bernardo ◽  
Carlos Lopes ◽  
...  
Keyword(s):  
Schistosoma Haematobium ◽  
Historical Perspective ◽  
Hiv Transmission ◽  
Parasite Infection ◽  
Urogenital Schistosomiasis ◽  
Host Parasite Interactions ◽  
Immunodeficiency Virus ◽  
Recent Outbreak ◽  
Host Parasite ◽  
Female Genital

Schistosomiasis is the most important helminthiasis worldwide in terms of morbidity and mortality. Most of the infections occurs in Africa, which about two thirds are caused by Schistosoma haematobium. The infection with S. haematobium is considered carcinogenic leading to squamous cell carcinoma (SCC) and urothelial carcinoma of the urinary bladder. Additionally, it is responsible for female genital schistosomiasis leading to infertility and higher risk of human immunodeficiency virus (HIV) transmission. Remarkably, a recent outbreak in Corsica (France) drew attention to its potential re-mergence in Southern Europe. Thus far, little is known related to host-parasite interactions that trigger carcinogenesis. However, recent studies have opened new avenues to understand mechanisms on how the parasite infection can lead cancer and other associated pathologies. Here, we present a historical perspective of schistosomiasis, and review the infection-associated pathologies and studies on host–parasite interactions that unveil tentative mechanisms underlying schistosomiasis-associated carcinogenesis.

Network Analysis: Ten Years Shining Light on Host–Parasite Interactions

2021 ◽  
Vol 37 (5) ◽  
pp. 445-455
Author(s):  
Rogini Runghen ◽  
Robert Poulin ◽  
Clara Monlleó-Borrull ◽  
Cristina Llopis-Belenguer
Keyword(s):  
Network Analysis ◽  
Host Parasite Interactions ◽  
Host Parasite

Host-Parasite Interactions of Tropical Bats in Puerto Rico

2009 ◽  
Vol 11 (1) ◽  
pp. 157-162 ◽  
Author(s):  
Kristle Krichbaum ◽  
Sarah Perkins ◽  
Michael R. Gannon
Keyword(s):  
Puerto Rico ◽  
Host Parasite Interactions ◽  
Host Parasite

scholarly journals Prospects of Using High-Throughput Proteomics to Underpin the Discovery of Animal Host–Nematode Interactions

Pathogens ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 825
Author(s):  
Tao Wang ◽  
Robin Gasser
Keyword(s):  
Mass Spectrometry ◽  
High Throughput ◽  
Anthelmintic Resistance ◽  
Nematode Species ◽  
Economic Losses ◽  
Future Research ◽  
Parasitic Nematodes ◽  
Public Health Burden ◽  
Host Parasite Interactions ◽  
Host Parasite

Parasitic nematodes impose a significant public health burden, and cause major economic losses to agriculture worldwide. Due to the widespread of anthelmintic resistance and lack of effective vaccines for most nematode species, there is an urgent need to discover novel therapeutic and vaccine targets, informed through an understanding of host–parasite interactions. Proteomics, underpinned by genomics, enables the global characterisation proteins expressed in a particular cell type, tissue and organism, and provides a key to insights at the host–parasite interface using advanced high-throughput mass spectrometry-based proteomic technologies. Here, we (i) review current mass-spectrometry-based proteomic methods, with an emphasis on a high-throughput ‘bottom-up’ approach; (ii) summarise recent progress in the proteomics of parasitic nematodes of animals, with a focus on molecules inferred to be involved in host–parasite interactions; and (iii) discuss future research directions that could enhance our knowledge and understanding of the molecular interplay between nematodes and host animals, in order to work toward new, improved methods for the treatment, diagnosis and control of nematodiases.

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