A compendium of molecules involved in vector-pathogen interactions pertaining to malaria
- Sreelakshmi K Sreenivasamurthy†1,
- Gourav Dey†1,
- Manjula Ramu1,
- Manish Kumar1,
- Manoj K Gupta1,
- Ajeet K Mohanty2,
- HC Harsha1,
- Pushkar Sharma3,
- Nirbhay Kumar4,
- Akhilesh Pandey5,
- Ashwani Kumar2 and
- TS Keshava Prasad1Email author
© Sreenivasamurthy et al.; licensee BioMed Central Ltd. 2013
Received: 24 January 2013
Accepted: 24 June 2013
Published: 26 June 2013
Malaria is a vector-borne disease causing extensive morbidity, debility and mortality. Development of resistance to drugs among parasites and to conventional insecticides among vector-mosquitoes necessitates innovative measures to combat this disease. Identification of molecules involved in the maintenance of complex developmental cycles of the parasites within the vector and the host can provide attractive targets to intervene in the disease transmission. In the last decade, several efforts have been made in identifying such molecules involved in mosquito-parasite interactions and, subsequently, validating their role in the development of parasites within the vector. In this study, a list of mosquito proteins, which facilitate or inhibit the development of malaria parasites in the midgut, haemolymph and salivary glands of mosquitoes, is compiled. A total of 94 molecules have been reported and validated for their role in the development of malaria parasites inside the vector. This compendium of molecules will serve as a centralized resource to biomedical researchers investigating vector-pathogen interactions and malaria transmission.
KeywordsKnockdown RNAi Gene silencing Plasmodium Anopheles Oocyst Sporozoite
Malaria continues to be one of the most debilitating mosquito-borne diseases. According to the WHO World Malaria Report in 2011, 216 million cases of malaria were reported in the year 2010, resulting in 655,000 deaths, of which 86% were children below five years of age. A total of 41 different species of Anopheles mosquitoes act as vectors for transmission of human malaria . Around 19 of them have been found to play a major role in disease-transmission across Asia-Pacific . Increasing instances of pathogens gaining resistance to the first-line of drugs and replacement anti-malarials have complicated the scenario of disease control in endemic areas. One of the approaches adopted towards limiting the spread of disease is to control the vector population by the reduction of breeding sites and use of insecticides and by minimizing mosquito-human contacts through the use of mosquito nets impregnated with insecticides. Though these measures have been largely effective, the development of resistance to insecticides coupled with the increased adaptability of the pathogen susceptible strains of vectors have emphasized the need for the development of alternative approaches to intervene the transmission of malaria .
Scientific literature was searched for molecules involved in infection of the vector by Plasmodium species. In addition to a keyword search for knockdown studies in mosquitoes, several author specific searches were also performed to retrieve articles relevant to vector-pathogen interactions. These were then screened for articles reporting the effect of RNA silencing on the rate of infection. Articles with the reports of RT-PCR experiments, which had further verified the reduction of mRNA expression, were also considered for annotation. From these articles, proteins that resulted in significant changes in the rate of infection upon gene silencing were annotated. These proteins were further segregated into three major groups – i) molecules involved in midgut invasion; ii) molecules involved in melanization; and iii) molecules involved in salivary gland invasion. Molecular conditions brought about by gene silencing events, which resulted in increased numbers of oocysts at midgut lamina and sporozoites at salivary glands, were inferred to promote parasite growth and the corresponding gene or genes were deemed to be inhibitory to parasite growth. Similarly, increased melanization of ookinetes was referred to as negative effect on parasite growth.
Summary of molecules involved in vector-Plasmodium interactions
Molecules involved in midgut invasion
Fusion of male and female gametes within the midgut of the mosquitoes results in the formation of zygotes and ookinetes, which then invade epithelium of the midgut and migrate to the basal lamina to form oocysts. The invasion of mosquito midgut by pathogens provides a critical step that involves adhesion to the midgut epithelia of the vector. Successful recognition and invasion of midgut epithelia by ookinetes is dependent on molecules that either facilitate or inhibit the parasite development. For instance, alanyl aminopeptidase N (APN1) was reported as a surface recognition molecule in the mosquito midgut . Epithelial invasion by the ookinetes is followed by the transformation of ookinetes to oocysts in the basal lamina. Seventy eight mosquito proteins were shown to be involved in midgut invasion by ookinetes and parasite survival, by survey of scientific literature.
Proteins such as TEP1 and LRIM1 are known to recognize the invading ookinetes and trigger immune responses in mosquitoes (Additional file 1) [8, 16, 19, 20]. C-type lectin 4 (CTL4), caspar and cactus are found to negatively regulate the immune responses, resulting in a decreased oocyst count upon their silencing [8, 21]. The proteins which generated complete refractoriness in the vector upon silencing may be the target of choice for future studies to block disease transmission. Heat shock protein, HSC3 resulted in decreased oocyst count upon knocking down in case of Anopheles gambiae and Plasmodium falciparum. However, in case of Anopheles stephensi infected with Plasmodium yoelii, it resulted in increased oocyst count . Similarly gastrin/cholecystokinin receptor 1 (GPRCCK1) also showed increase in the oocyst count upon infection of An. gambiae with Plasmodium berghei and decrease upon infection with P. falciparum (Additional file 2) .
Certain proteins such as clip-domain serine protease 17 (CLIPB17) showed no significant change in the number of oocysts upon its silencing. However, in combination with CTL4, silencing of CLIPB17 resulted in a significant decrease of oocysts (Additional files 1 and 3) . Similarly, ARC P21 and ARC P41 subunits of the actin related protein complex shows no effect on the number of oocysts formed, when silenced individually. However, a double knockdown of these genes resulted in the formation of larger number of oocysts .
Molecules involved in melanization
Of the many ookinetes that are formed in the mosquito midgut, only a handful develops into a mature oocyst that upon rupturing, release sporozoites into the haemocoel. Sporozoites then migrate towards salivary glands of mosquito through haemolymph. Phagocytosis and melanin deposition on the surface of invading parasites represents the major immune responses in arthropods [23, 24]. The mechanism of these responses is not completely understood. However, various models have been proposed. Melanization of the invading ookinetes possibly results in the reduced formation of oocysts, thereby preventing transmission.
A total of 22 molecules have been identified thus far, to play a role in the melanization of ookinetes within the mosquitoes. Gene silencing studies undertaken to understand the biology of melanogenesis, revealed the role of serine proteases, such as CLIPB4, CLIPB8 and TEP1 [10, 21]. Silencing of these serine proteases resulted in the reduction in melanization, when infected with P. berghei. Among the 22 genes affecting the rate of melanization, two proteins SRPN6 and TEP1 were found to affect oocyst and sporozoite counts along with melanization of ookinetes. SRPN6 was reported to increase the melanization rates in refractory strains of An. gambiae, but not in susceptible G3 strain or An. stephensi. However, knockdown of SRPN6 in combination with CTL4 was reported to significantly increase the rate of melanization in susceptible G3 strain of An. gambiae. Fourteen of them were found to be associated with the oocyst invasion and melanization. Silencing of seven genes including clip-domain serine proteases, such as CLIPA2 and CLIPA5 were found to increase the rate of melanization and decrease the oocyst count [17, 21, 25, 26]. Knocking down of 3 genes (APL1C, LRIM1 and TEP1) showed decreased melanization of ookinetes and increased number of oocysts [8, 10, 16, 17, 20, 27–34]. However, silencing of CLIPB3 and CLIPA8 resulted in the reduction of both melanization and oocyst counts (Additional files 1 and 4, Figure 3) . Some investigations revealed that melanization may not necessarily affect parasite invasion, and may be involved in the disposal of dead parasites [21, 35].
Molecules involved in salivary gland invasion
Sporozoites that survive mosquito immune response in the midgut lamina and haemocoel of mosquitoes migrate to salivary glands through haemolymph. Losses of up to 80 - 90% sporozoites have been reported, during their migration to the salivary glands through haemolymph by various mechanisms that are not yet completely understood . Effective and specific associations of sporozoite surface antigens such as TRAP, with receptors such as saglin on the salivary glands of mosquitoes initiate the salivary gland invasion by sporozoites . Plasmodium responsive salivary 1 (PRS1), ESP, peptide-O-xylosyltransferase 1 (OXT1) and SRPN6 have been identified to play a crucial role in parasite invasion of both midgut and salivary glands. Silencing of PRS1, ESP, retinoid and fatty-acid binding glycoprotein (RFABG) and OXT1 resulted in decreased oocyst and sporozoite counts (Additional files 1 and 5, Figure 3), whereas SRPN6 and TEP1 silencing resulted in an increase in production of oocysts and sporozoites [7, 37–40].
The sporozoites undergo changes in their membrane proteins upon salivary gland invasion, which enable them to successfully infect the vertebral hosts . Salivary gland invasion by the sporozoites and their development within is an essential step in the parasite life cycle and effective transmission of Plasmodium. Blocking of these processes could disrupt the parasite development in mosquitoes and suppress malaria transmission.
Blocking the vector-parasite interactions can be one of the novel approaches to control transmission of vector borne infections. Several proteins of mosquitoes have been involved in the regulation of maturation of malaria parasites within the vector. Transmission-blocking vaccine (TBV) is one of the strategies, which specifically target such proteins and block parasite invasion and survival. TBVs when injected in vertebrate host as purified antigens induce production of antibodies in the host against the corresponding antigens. These antibodies then interfere with the parasite transmission in the vector following blood meal on an infected and vaccinated individual . Furthermore, engineered anti-Plasmodium immunity in transgenic mosquitoes has shown increased resistance in the vector against the pathogen . Such genetically modified insects have been successful in replacing the wild type population .
Among the molecules listed in this study, 40 proteins were found to assist in parasite survival at different stages. Proteins which are involved in vector immunity resulted in increased number of oocysts or sporozoites upon being knocked down, showing their involvement in suppressing the parasite during infection. A resource of such proteins would provide a platform for other studies, to identify the potential targets and to translate the outcome as possible mechanism for malaria control. Such novel approaches along with the conventional ways of vector control and infection treatment may lead to accomplish the vision of malaria eradication.
World Health Organization
We thank the Department of Biotechnology, Government of India for research support to the Institute of Bioinformatics, Bangalore. Sreelakshmi K. Sreenivasamurthy and Gourav Dey are recipients of Junior Research Fellowship from the University Grants Commission (UGC), Government of India. Manjula Ramu and Manish Kumar are recipients of Junior Research Fellowship from the Council of Scientific and Industrial Research (CSIR), Government of India. Manoj Kumar Gupta is a recipient of Senior Research Fellowship from CSIR, Government of India. HC Harsha is a Wellcome Trust-DBT India Alliance Early Career Fellow. Research in the laboratories of Akhilesh Pandey and Nirbhay Kumar is supported by NIH grants. The funding bodies had no role in the collection, analysis and interpretation of data, in the writing of the manuscript, and in the decision to submit the manuscript for publication.
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