scholarly journals The in vivo transcriptome of Schistosoma mansoni in the prominent vector species Biomphalaria pfeifferi with supporting observations from Biomphalaria glabrata

2019 ◽  
Vol 13 (9) ◽  
pp. e0007013 ◽  
Author(s):  
Sarah K. Buddenborg ◽  
Bishoy Kamel ◽  
Ben Hanelt ◽  
Lijing Bu ◽  
Si-Ming Zhang ◽  
...  
2018 ◽  
Author(s):  
Sarah K. Buddenborg ◽  
Bishoy Kamel ◽  
Ben Hanelt ◽  
Lijing Bu ◽  
Si-Ming Zhang ◽  
...  

ABSTRACTBackgroundThe full scope of the genes expressed by schistosomes during intramolluscan development has yet to be characterized. Understanding the gene products deployed by larval schistosomes in their snail hosts will provide insights into their establishment, maintenance, asexual reproduction, ability to castrate their hosts, and their prolific production of human-infective cercariae. Using the Illumina platform, the intramolluscan transcriptome ofSchistosoma mansoniwas investigated in field-derived specimens of the prominent vector speciesBiomphalaria pfeifferiat 1 and 3 days post infection (d) and from snails shedding cercariae. TheseS. mansonisamples were derived from the same snails used in our complementaryB. pfeifferitranscriptomic study. We supplemented this view with microarray analyses ofS. mansonifromB. glabrataat 2d, 4d, 8d, 16d, and 32d.Principal FindingsTranscripts representing at least 7,740 (66%) of knownS. mansonigenes were expressed during intramolluscan development, with the greatest number expressed in snails shedding cercariae. Many transcripts were constitutively expressed throughout development featuring membrane transporters, and metabolic enzymes involved in protein and nucleic acid synthesis and cell division. Several proteases and protease inhibitors were expressed at all stages, including some proteases usually associated with cercariae. Transcripts associated with G-protein coupled receptors, germ cell perpetuation, and stress responses and defense were well represented. We noted transcripts homologous to planarian anti-bacterial factors, several neural development or neuropeptide transcripts including neuropeptide Y, and receptors that may be associated with schistosome germinal cell maintenance and that could also impact host reproduction. In at least one snail the presence of larvae of another digenean species (an amphistome) was associated with repressedS. mansonitranscriptional activity.Conclusions/SignificanceThisin vivostudy, particularly featuring field-derived snails and schistosomes, provides a distinct view from previous studies of development of cultured intramolluscan stages from lab-maintained organisms. We found many highly represented transcripts with suspected or unknown functions, with connection to intramolluscan development yet to be elucidated.AUTHOR SUMMARYSchistosoma mansoniis one of the most important schistosome species causing the neglected tropical disease human intestinal schistosomiasis. By focusing onS. mansoni in vivowith its broadly distributed sub-Saharan African snail intermediate host,Biomphalaria pfeifferi, we uncover new insights and basic knowledge of this host-parasite relationship that are critical for understanding schistosomiasis transmission. We show thatin vivostudies, particularly using field-derived specimens, provides a distinct view from the uniformed transcriptional responses traditionally seen fromin vitrostudies onS. mansoniandBiomphalariasnails. With the growing consensus that we need to supplement chemotherapy with other control methods, understanding howS. mansoniinteracts with its obligatory snail host becomes integral for future planning of control programs. The data provided within provides specific analysis on how the schistosomes successfully protect themselves from host defenses and the necessary transcriptional responses required for its amplifying asexual proliferation that result in human-infective cercariae.


Parasitology ◽  
1993 ◽  
Vol 107 (3) ◽  
pp. 275-285 ◽  
Author(s):  
S. N. Thompson ◽  
R. W. K. Lee ◽  
V. Mejia-Scales ◽  
M. Shams El-Din

SummaryInfection by Schistosoma mansoni resulted in morphological and biochemical changes to the foot of its intermediate host, Biomphalaria glabrata. Migration through, and emergence of cercariae from, the foot was observed and evidenced by lesions on the ciliated foot surface. This was accompanied by a significant decrease in the velocity of movement by infected individuals. In vivo31P NMR spectral analyses demonstrated that the foot of infected snails had a lower phosphoarginine (PA)/adenosine 5' triphosphate (ATP) ratio than that of uninfected controls. Moreover, kinetic experiments, employing saturation transfer, demonstrated the pseudo-first-order rate constant for the arginine kinase-catalysed exchange reaction in the forward direction, that is, PA→ATP was decreased by infection. The reverse reaction was not observed by the NMR methods used. PA was depleted upon exposure to hypoxic conditions suggesting its traditional role in preserving ATP level. Partly oxidized metabolic end-products were not observed in snails maintained under aerobic conditions, but succinate, propionate, acetate and lactate rapidly accumulated under hypoxic conditions.


Author(s):  
M. Graber ◽  
Jacques Euzéby ◽  
J. Gevrey

Les auteurs décrivent une méthode d'élevage de Biomphalaria glabrata, Say, au laboratoire, méthode nécessitant l'emploi successif et, dans des conditions qui sont bien précisées, de bacs de ponte et de bacs de croissance. Bien que concernant un Planorbe hôte intermédiaire de Schistosoma mansoni, l'agent de la bilharziose intestinale humaine, les renseignements fournis présentent un certain intérêt en médecine vétérinaire, car ils peuvent, dans leur ensemble, être transposés à d'autres mollusques vecteurs de Trématodoses animales (Fasciolose, paramphistomose, bilharzioses à Schistosoma bovis et à Schistosoma mattheei): Limnaea natalensis, Biomphalaria pfeifferi, Bulins appartenant aux genres Physopsis, Bulinus s. str. (toute la série polyploïde) et Pyrgophysa. En outre, lorsque les conditions climatiques s'y prêtent, cette méthode, simple et pratique, permet de disposer constamment, et quelle que soit la saison, d'importantes populations de Biomphalaria glabrata destinées à diverses recherches d'ordre général, notamment les essais de molluscicides et la lutte biologique contre les mollusques vecteurs, recherches qui intéressent à la fois la médecine humaine et la médecine vétérinaire tropicale notamment


Genes ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 38 ◽  
Author(s):  
Jacob R. Hambrook ◽  
Abdullah A. Gharamah ◽  
Emmanuel A. Pila ◽  
Solomon Hussein ◽  
Patrick C. Hanington

Gastropod molluscs, which have co-evolved with parasitic digenean trematodes for millions of years, utilize circulating heamocytes as the primary method of containing and killing these invading parasites. In order to do so, they must generate suitable amounts of haemocytes that are properly armed to kill parasitic worms. One method by which they generate the haemocytes required to initiate the appropriate cell mediated immune response is via the production and post-translational processing of granulins. Granulins are an evolutionarily conserved family of growth factors present in the majority of eukaryotic life forms. In their pro-granulin form, they can elicit cellular replication and differentiation. The pro-granulins can be further processed by elastase to generate smaller granulin fragments that have been shown to functionally differ from the pro-granulin precursor. In this study, we demonstrate that in vivo addition of Biomphalaria glabrata pro-granulin (BgGRN) can reduce Schistosoma mansoni infection success in numerous Biomphalaria sp. when challenged with different S. mansoni strains. We also demonstrate that cleavage of BgGRN into individual granulin subunits by elastase results in the stimulation of haemocytes to produce reactive oxygen species.


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