Sensory Protein Kinase Signaling in Schistosoma mansoni Cercariae: Host Location and Invasion

نویسندگان

  • Margarida Ressurreição
  • Ruth S. Kirk
  • David Rollinson
  • Aidan M. Emery
  • Nigel M. Page
  • Anthony J. Walker
چکیده

Schistosoma mansoni cercariae display specific behavioral responses to abiotic/biotic stimuli enabling them to locate and infect the definitive human host. Here we report the effect of such stimulants on signaling pathways of cercariae in relation to host finding and invasion. Cercariae exposed to various light/temperature regimens displayed modulated protein kinase C (PKC), extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (p38 MAPK) activities, with distinct responses at 37 °C and intense light/dark, when compared to 24 °C under normal light. Kinase activities were localized to regions including the oral sensory papillae, acetabular ducts, tegument, acetabular glands, and nervous system. Furthermore, linoleic acid modulated PKC and ERK activities concurrent with the temporal release of acetabular gland components. Attenuation of PKC, ERK, and p38 MAPK activities significantly reduced gland component release, particularly in response to linoleic acid, demonstrating the importance of these signaling pathways to host penetration mechanisms.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Mast Cells Kinetics during Experimental Schistosomiasis mansoni in Mice

Increased number of mast cells at the site of infection is widely regarded as important host defense against parasites. The kinetics of mucosal mast cells and connective tissue mast cells responses were studied in the intestines of 68 female CFLP mice infected with 100 Schistosoma mansoni cercariae. The number of mucosal mast cells and the connective tissue mast cells increased from week 3 and ...

متن کامل

Role of Cathepsin B in Schistosoma japonicum Infection

roteases, including cysteine-, serine-, threonine-, aspartate-, and metallo-proteases, are a group of enzymes that have the catalytic ability to hydrolyze or digest peptide bonds of proteins. Proteases play important roles in host invasion, hemoglobin degradation, transformation and immune invasion of schistosomes. The gut cathepsin B of all schistosomes including S. japonicum, S. mansoni and S...

متن کامل

Proteomic Analysis of Schistosoma mansoni Cercarial Secretions*□S

Schistosomiasis is a global health problem caused by several species of schistosome blood flukes. The initial stage of infection is invasion of human skin by a multicellular larva, the cercaria. We identified proteins released by cercariae when they are experimentally induced to exhibit invasive behavior. Comparison of the proteome obtained from skin lipid-induced cercariae (the natural activat...

متن کامل

Proteomic Analysis of Skin Invasion by Blood Fluke Larvae

BACKGROUND During invasion of human skin by schistosome blood fluke larvae (cercariae), a multicellular organism breaches the epidermis, basement membrane, and dermal barriers of skin. To better understand the pathobiology of this initial event in schistosome infection, a proteome analysis of human skin was carried out following invasion by cercariae of Schistosoma mansoni. METHODOLOGY AND RE...

متن کامل

Vaccination of mice with radiation-attenuated larvae of Schistosoma japonicum or S. mansoni

Introduction Partial protection against challenge infections with normal cercariae of Schistosoma mansoni or S. japonicum has been induced by immunization with attenuated cercariae of either species. Immunization was successful in a number of different hosts including laboratory rodents and larger mammals. In most cases cercariae or schistosomula were irradiated with gamma or X-irradiation. The...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 212  شماره 

صفحات  -

تاریخ انتشار 2015