Host–parasite interactions and ecology of the malaria parasite—a bioinformatics approach

2018 ◽  
Author(s):  
Dariusz Izak ◽  
Joanna Klim ◽  
Szymon Kaczanowski
Keyword(s):  
Malaria Parasite ◽  
Host Parasite Interactions ◽  
Host Parasite

scholarly journals Functional genomics of simian malaria parasites and host–parasite interactions

2019 ◽  
Vol 18 (5) ◽  
pp. 270-280 ◽  
Author(s):  
Mary R Galinski
Keyword(s):  
Functional Genomics ◽  
Malaria Parasite ◽  
Parasite Species ◽  
Plasmodium Knowlesi ◽  
New World Monkeys ◽  
Malaria Parasites ◽  
Zoonotic Infections ◽  
Simian Malaria ◽  
Host Parasite Interactions ◽  
Host Parasite

AbstractTwo simian malaria parasite species, Plasmodium knowlesi and Plasmodium cynomolgi, cause zoonotic infections in Southeast Asia, and they have therefore gained recognition among scientists and public health officials. Notwithstanding, these species and others including Plasmodium coatneyi have served for decades as sources of knowledge on the biology, genetics and evolution of Plasmodium, and the diverse ramifications and outcomes of malaria in their monkey hosts. Experimental analysis of these species can help to fill gaps in knowledge beyond what may be possible studying the human malaria parasites or rodent parasite species. The genome sequences for these simian malaria parasite species were reported during the last decade, and functional genomics research has since been pursued. Here research on the functional genomics analysis involving these species is summarized and their importance is stressed, particularly for understanding host–parasite interactions, and potentially testing novel interventions. Importantly, while Plasmodium falciparum and Plasmodium vivax can be studied in small New World monkeys, the simian malaria parasites can be studied more effectively in the larger Old World monkey macaque hosts, which are more closely related to humans. In addition to ex vivo analyses, experimental scenarios can include passage through Anopheline mosquito hosts and longitudinal infections in monkeys to study acute and chronic infections, as well as relapses, all in the context of the in vivo host environment. Such experiments provide opportunities for understanding functional genomic elements that govern host–parasite interactions, immunity and pathogenesis in-depth, addressing hypotheses not possible from in vitro cultures or cross-sectional clinical studies with humans.

Oxidative stress in malaria parasite-infected erythrocytes: host–parasite interactions

2004 ◽  
Vol 34 (2) ◽  
pp. 163-189 ◽  
Author(s):  
Katja Becker ◽  
Leann Tilley ◽  
Jonathan L. Vennerstrom ◽  
David Roberts ◽  
Stephen Rogerson ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Malaria Parasite ◽  
Host Parasite Interactions ◽  
Host Parasite

scholarly journals Large, rapidly evolving gene families are at the forefront of host–parasite interactions inApicomplexa

Parasitology ◽  
2014 ◽  
Vol 142 (S1) ◽  
pp. S57-S70 ◽  
Author(s):  
ADAM J REID
Keyword(s):  
Gene Expression ◽  
Malaria Parasite ◽  
Gene Expression Regulation ◽  
Protein Localization ◽  
Animal Health ◽  
Gene Families ◽  
Sequence Diversity ◽  
Genomic Context ◽  
Host Parasite Interactions ◽  
Host Parasite

SUMMARYTheApicomplexais a phylum of parasitic protozoa, which includes the malaria parasitePlasmodium, amongst other species that can devastate human and animal health. The past decade has seen the release of genome sequences for many of the most important apicomplexan species, providing an excellent basis for improving our understanding of their biology. One of the key features of each genome is a unique set of large, variant gene families. Although closely related species share the same families, even different types of malaria parasite have distinct families. In some species they tend to be found at the ends of chromosomes, which may facilitate aspects of gene expression regulation and generation of sequence diversity. In others they are scattered apparently randomly across chromosomes. For some families there is evidence they are involved in antigenic variation, immune regulation and immune evasion. For others there are no known functions. Even where function is unknown these families are most often predicted to be exposed to the host, contain much sequence diversity and evolve rapidly. Based on these properties it is clear that they are at the forefront of host–parasite interactions. In this review I compare and contrast the genomic context, gene structure, gene expression, protein localization and function of these families across different species.

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
Sign in / Sign up

Export Citation Format

Share Document