- Open Access
Wide cross-reactivity between Anopheles gambiae and Anopheles funestus SG6 salivary proteins supports exploitation of gSG6 as a marker of human exposure to major malaria vectors in tropical Africa
- Cinzia Rizzo†1,
- Raffaele Ronca†2,
- Gabriella Fiorentino2,
- Valentina D Mangano1,
- Sodiomon B Sirima3,
- Issa Nèbiè3,
- Vincenzo Petrarca4, 5,
- David Modiano1, 5 and
- Bruno Arcà2Email author
© Rizzo et al; licensee BioMed Central Ltd. 2011
Received: 4 May 2011
Accepted: 27 July 2011
Published: 27 July 2011
The Anopheles gambiae gSG6 is an anopheline-specific salivary protein which helps female mosquitoes to efficiently feed on blood. Besides its role in haematophagy, gSG6 is immunogenic and elicits in exposed individuals an IgG response, which may be used as indicator of exposure to the main African malaria vector A. gambiae. However, malaria transmission in tropical Africa is sustained by three main vectors (A. gambiae, Anopheles arabiensis and Anopheles funestus) and a general marker, reflecting exposure to at least these three species, would be especially valuable. The SG6 protein is highly conserved within the A. gambiae species complex whereas the A. funestus homologue, fSG6, is more divergent (80% identity with gSG6). The aim of this study was to evaluate cross-reactivity of human sera to gSG6 and fSG6.
The A. funestus SG6 protein was expressed/purified and the humoral response to gSG6, fSG6 and a combination of the two antigens was compared in a population from a malaria hyperendemic area of Burkina Faso where both vectors were present, although with a large A. gambiae prevalence (>75%). Sera collected at the beginning and at the end of the high transmission/rainy season, as well as during the following low transmission/dry season, were analysed.
According to previous observations, both anti-SG6 IgG level and prevalence decreased during the low transmission/dry season and showed a typical age-dependent pattern. No significant difference in the response to the two antigens was found, although their combined use yielded in most cases higher IgG level.
Comparative analysis of gSG6 and fSG6 immunogenicity to humans suggests the occurrence of a wide cross-reactivity, even though the two proteins carry species-specific epitopes. This study supports the use of gSG6 as reliable indicator of exposure to the three main African malaria vectors, a marker which may be useful to monitor malaria transmission and evaluate vector control measures, especially in conditions of low malaria transmission and/or reduced vector density. The Anopheles stephensi SG6 protein also shares 80% identity with gSG6, suggesting the attractive possibility that the A. gambiae protein may also be useful to assess human exposure to several Asian malaria vectors.
After more than a century from the discovery of the role of Anopheles mosquitoes in the transmission of Plasmodium parasites, malaria is still one of the leading causes of human morbidity and mortality. Currently, the malaria toll is especially high among young children in sub-Saharan Africa, where transmission of the most deadly malaria parasite, Plasmodium falciparum, is mainly accomplished by two members of the Anopheles gambiae species complex (i.e. A. gambiae and Anopheles arabiensis, subgenus Cellia, Pyretophorus Series) and by Anopheles funestus (subgenus Cellia, Myzomyia Series) . Proper evaluation of malaria transmission intensity, of seasonal and temporal variation of vector density and of the efficacy of anti-parasite and anti-vector control measures play crucial roles in the framework of anti-malaria strategies.
Assessment of malaria transmission intensity is currently based on both parasitological and entomological measures and a key parameter is the entomological inoculation rate (EIR), which accounts for human exposure to parasite-carrying mosquitoes. However, entomological measurements are not only expensive and labor-intensive but, sometime, also difficult or impossible to apply: for example in conditions of low transmission intensity and/or low mosquito density, or for logistic restrictions. Therefore, additional and/or alternative methods to evaluate Anopheles density and human exposure to malaria vectors would be extremely valuable allowing for epidemiological studies also in settings where classical entomological methods are of problematic use. During blood feeding, mosquitoes inject into their hosts a complex mixture of salivary components whose main role is to facilitate haematophagy by counteracting the haemostatic, inflammatory and immune responses of vertebrates [2, 3]. These salivary components also elicit into hosts an immune response with production of anti-saliva antibodies. For example, at least 10-15 protein bands recognized by human IgG can be detected by western blot using A. gambiae salivary gland protein extracts and sera from exposed individuals from a malaria hyperendemic area (B.A., unpublished observations). Several reports support the concept that measurement of this antibody response to saliva may represent an indicator of human exposure to Anopheles bites and malaria risk, as well as a tool to evaluate efficacy of insecticide-treated nets (ITNs) [4–8]. Moreover, the identification of Anopheles-specific proteins, i.e. not found in other mosquitoes or blood feeding arthropods, offers the opportunity to use as markers genus-specific recombinant salivary antigens instead of saliva [2, 9]. This enables for a significant improvement of the methodology increasing both the accuracy and the specificity by overcoming the need of obtaining large amount of saliva and potential problems of reproducibility and cross-reactivity.
Conveniently, vector's salivary antigens could be used in parallel to Plasmodium antigens to assess, by serological determination of antibody levels, both exposure of humans to Anopheles mosquitoes and malaria transmission intensity [10–14]. This immune response to salivary antigens would represent a direct measure of intensity of mosquito biting activity on humans, both at the population and at individual level, and could provide a few additional advantages. First, it may allow to assess Anopheles exposure in children, which is presently unworkable for ethical reasons (the method currently in use is based on human landing catches on adult volunteers). Second, it would be very helpful to evaluate the impact of anti-vector control measures on exposure of humans to Anopheles bites. Third, it would be a tool especially needed for epidemiological assessments in areas of low malaria transmission, which are currently increasing as a consequence of the decline of the malaria burden in several areas of sub-Saharan Africa . Finally, it might be the appropriate tool to verify if, and eventually to what extent, the mosquito biting activity is heterogeneously distributed within a population. Indeed, according to the so-called heterogeneous biting model, mosquito biting may be unequally distributed, with few people receiving most of the mosquito bites (i.e. 20-30% of the population getting 70-80% of the bites). Heterogeneous biting has broad implications for malaria epidemiology and control and, as recently suggested, may provide a plausible explanation for inconsistencies related to malaria transmission dynamics and modelling .
Toward the development of serological markers of exposure to malaria vectors, attention was focused on gSG6 (g ambiae S alivary G land protein 6), a small protein initially identified in A. gambiae, where it is specifically expressed in the salivary glands of adult female mosquitoes . Its specific function awaits full clarification; however, gSG6 must play some relevant role in haematophagy since its depletion by RNAi increases probing time and affects blood feeding ability . Afterwards, members of the SG6 protein family have been identified in the salivary transcriptomes of additional anopheline mosquitoes, but in no other living organisms, pointing to its genus-specificity and blood feeding role. Among the few anophelines analysed so far the SG6 protein is present in species belonging to the subgenus Cellia (A. gambiae species complex, A. funestus, Anopheles stephensi) and in Anopheles freeborni (a member of the subgenus Anopheles), but it is notably absent in Anopheles darlingi, a member of the subgenus Nyssorhynchus and vector of malaria in Central and South America . This observation suggests that SG6 family members may be widely distributed among the main African and Asian malaria vectors, but most likely absent in South American ones.
Given the anopheline-specificity and previous indications of the immunogenicity to humans of gSG6-based peptides , the A. gambiae gSG6 protein was expressed in recombinant form and the anti-gSG6 IgG response was analysed in a population from a malaria hyperendemic area of Burkina Faso. This study provided experimental evidence that gSG6 may be a good candidate as serological marker of human exposure to A. gambiae , although full validation in different epidemiological settings (i.e. low transmission conditions, macro-geographic scale) is needed. Moreover, since malaria is transmitted by multiple and often sympatric vectors, an ideal salivary marker should allow to estimate exposure to all the major vector species in the study area. The A. gambiae gSG6 protein is highly conserved among members of the A. gambiae species complex (99% identity with the A. arabiensis homologue, aSG6), whereas it is more distantly related (80%, 70/87 residues) to the A. funestus protein (fSG6). It is likely that a certain degree of cross-reactivity to the two protein exists, but the extent of the overlap of the human IgG response to gSG6 and fSG6 proteins is unknown. Some indications in this direction have been obtained using the 23 aa long gSG6-P1 peptide, which encompasses the gSG6 N-terminal region . However, this peptide is less sensitive in comparison to the whole protein (approx 5-fold) and, therefore, it would be important to experimentally validate the efficacy of using the antibody response to the gSG6 protein as marker of exposure to the three main malaria vectors in tropical Africa. The aim of this study was to evaluate cross-reactivity of human sera from exposed individuals to the gSG6 and fSG6 proteins. To this purpose the A. funestus fSG6 was expressed in recombinant form and the IgG response to fSG6, gSG6 and to an equimolar mixture of the two proteins was compared by ELISA using sera of individuals from a malaria hyperendemic area of Burkina Faso.
Study area and entomological observations
Surveys were carried out in the village of Barkoumbilen (~35 km NE of Ouagadougou, Burkina Faso), a rural settlement inhabited by the two ethnic groups Mossi and Rimaibé. The area was characterized by intense P. falciparum transmission, mostly linked to the rainy season (from June to October), with entomological inoculation rates >100/person/year. Malaria prevalence was very high, P. falciparum representing about 95% of malaria infections, and infection rates ranged, during the high transmission season, from 60% to 90% according to age group. Lower prevalences, ranging between 40% and 80%, were observed during the dry low transmission season. The study protocol was approved by the Technical Committee of the Centre National de Lutte contre le Paludisme of the Ministry of Health of Burkina Faso. Oral informed consent for multiple immuno-parasitological, clinical and entomological surveys was obtained from the Mossi-Rimaibè community living in the village of Barkoumbilen. A total of 335 sera collected from individuals of the Mossi ethnic group in 1994 at the beginning (August '94) and at the end (October '94) of the high transmission/rainy season, as well as in the following low transmission/dry season (March '95) were analysed in this study. Sera from 48 Roman citizens (1-56 years old) who were referred to a city hospital for routine blood testing were used as a control. Additional information on samples size and average age for each survey can be found in the legends to Figures. Entomological measures were based on indoor pyrethrum spray catches carried out monthly between August and November '94 and in March '95 (12 catches/month). A total of 1,653 female Anopheles mosquitoes were identified: among these 1,479 were members of the A. gambiae species complex (A. gambiae or A. arabiensis) and 174 were A. funestus. Additional details on the study site and on entomological and parasitological aspects have been previously reported and can be found elsewhere [22–24].
Protein expression and purification
The A. funestus SG6 protein (fSG6) was expressed as N-terminal His-tagged recombinant protein in the E. coli vector pET28b(+) (Novagen). Briefly, the region encoding the mature fSG6 protein was PCR amplified using as template genomic DNA extracted from a single mosquito collected in 2008 in the Bobo-Dioulasso area, Burkina Faso. Amplification was performed using the Pfx DNA polymerase (Invitrogen) and the oligonucleotide primers G6fu-Nde (5'- GTCTCATATG GAAAAGGTTTGGGTCGATCG-3'OH) and G6fu-Eco (5'- GTCTGAATTC TCACTGTTCCAGGAAGGGTTTG -3'OH). Directional cloning in the Nde I/Eco RI-digested pET28b vector yielded the pET-fSG6 expression vector, that was sequenced and then introduced into competent BL21(DE3)RIL E. coli cells (Stratagene). Expression and purification was essentially performed as previously reported for the A. gambiae gSG6 protein  with few modifications. After overnight growth (37°C, LB medium) 5 ml of the saturated culture were transferred into 400 ml of LB medium and grown up to 0.8 OD600 before starting induction by IPTG (0.1 mM). After 4 hours cells were harvested and the pellet resuspended in 20 ml of 50 mM Tris-HCl pH 8.0, 50 mg/ml lysozyme and sonicated. Inclusion bodies (IB) were collected by centrifugation (15,000 g, 20 min, 4°C), resuspended in extraction buffer (50 mM Tris-HCl pH 8.0, 2 M Urea, 5 mM EDTA, 1% Triton-X100), washed twice (50 mM Tris-HCl pH 8.0, 2 M Urea) and centrifuged as above. Proteins from IB were solubilized by gentle shaking over-night (5 ml of 20 mM Na2HPO4, 6 M Guanidine-HCl, 0.5 M NaCl, 5 mM Imidazole, pH 8.0), centrifuged (20000 g, 30 min, 4°C) and subjected to affinity chromatography under denaturing conditions (HisTrap, GE Healthcare) according to manufacturer's instructions. Fractions containing the His-tagged fSG6 were identified by SDS-PAGE and pooled. Refolding of this fSG6-enriched fraction was carried out by rapid dilution in 20 volumes of refolding buffer (100 mM Tris-HCl pH 8.0, 500 mM L-Arg, 300 mM NaCl, 5 mM L-Glutathione reduced, 0.5 mM L-Glutathione oxidized) and left for 24 h at 4°C with low stirring. After centrifugation (20,000 g, 30 min, 4°C) the refolded proteins were concentrated by centrifugation in Amicon® Ultra (5 kDa MWCO, Millipore), dialyzed against 20 mM Tris-HCl pH 8.0 and further purified by anion exchange chromatography (HiTrapQ, GE Healthcare). Elution was carried out with a linear gradient 0 - 0.5 M NaCl in 18 column volumes. Fractions containing the fSG6 recombinant protein were identified by SDS-PAGE, pooled, concentrated and dyalized against 20 mM Tris-HCl pH 8.0, 150 mM NaCl. Concentration of the purified protein was estimated by the Bradford Protein Assay (Bio-Rad Laboratories). The yield of purified protein was of approximately 6 mg/l, however this is most likely susceptible to improvements since optimization of the procedure for the A. gambiae homologue allowed for higher recovery (~9-12 mg/l) as previously reported .
Enzyme-Linked ImmunoSorbent Assay SG6
ELISA was performed according to standard procedures. Maxisorp 96-well plates (Nunc M9410) were coated overnight at 4°C with 50 μl of the A. gambiae gSG6 (10 μg/ml), or the A. funestus fSG6 (10 μg/ml), or with an equimolar mixture of the two protein (10 μg/ml total) in coating buffer (15 mM Na2CO3, 35 mM NaHCO3, 3 mM NaN3, pH 9.6). After washing (four times) wells were blocked (3 hrs, RT) in 150 μl of 1% w/v skimmed dry milk in PBST (PBS Sigma P4417+0.05% Tween 20), washed again and incubated overnight at 4°C with 50 μl of serum (1:100) in blocking buffer. Sera were analysed in duplicate with each antigen and once without antigen (coating buffer only). Each plate included a two-fold dilution series (1:40 to 1:2560 final dilutions) of a standard African hyperimmune sera pool. After washing plates were incubated (3 hrs, RT) with 100 μl of polyclonal rabbit anti-human IgG/HRP antibody (Dako P0214, 1:5000 in blocking buffer). After washing as above the colorimetric development was carried out (15 min, RT in the dark) with 100 μl of o-phenylenediamine dihydrochloride (OPD, Sigma P8287). The reaction was terminated adding 25 μl of 2 M H2SO4 and the OD492 was determined using a microplate reader (BioTek Synergy HT). IgG levels were expressed as final OD calculated for each serum as the mean OD value with antigen minus the OD value without antigen. OD values were normalized using the titration curve as previously described . The normalized ODs were calculated using the Excel software (Microsoft) with a three variable sigmoid model and the Solver add-in application.
Sera whose duplicates showed a coefficient of variation (CV) >20% were not included into the analysis. The mean optical density (OD) of unexposed controls plus 3 standard deviations (SD) was used as cut-off value for seropositivity. Cut-off values were 0.140 for gSG6, 0.160 for fSG6 and 0.132 for the two antigens combined. Individuals showing OD values above the cut-off level for seropositivity were classified as responders. Multiple comparisons were performed by the Kruskal-Wallis test or, for matched groups, by the Friedman's test. Mann-Whitney U test was used to compare IgG levels among responders of two independent groups. The Wilcoxon matched-pairs test was used for comparison of two paired groups. Frequencies were compared by the chi-square test. All statistical analysis was performed using GraphPad Prism 5.0® statistical software (GraphPad Software Inc., La Jolla, CA).
Results and discussion
Expression and purification of the A. funestus SG6 protein
Study area and entomological data
Seasonal and age-dependent pattern of the IgG response to gSG6 and fSG6
In summary, both the seasonal and the age-related pattern of the anti-SG6 humoral response were very similar with the gSG6 and the fSG6 recombinant proteins, or with their combination, and recapitulated what previously observed in the same epidemiological setting with the A. gambiae gSG6 antigen alone .
Comparison of the IgG response to gSG6 and fSG6
Overall, the analysis of the humoral response of exposed individuals from a malaria hyperendemic area from Burkina Faso to the recombinant SG6 protein from A. gambiae and A. funestus indicates that there is wide cross-reactivity to these two antigens. Both IgG level and seroprevalence obtained with either the gSG6 or the fSG6 antigens were very similar, even in an epidemiological setting where A. gambiae and A. arabiensis, both members of the A. gambiae complex, are largely prevalent (>77%). Since the SG6 proteins from these two last species are 99% identical, these observations support the use of the A. gambiae gSG6 as a reliable marker to evaluate human exposure to the three main Afrotropical malaria vectors: A. gambiae, A. arabiensis and A. funestus. In addition, this study provides evidence that gSG6 and fSG6 proteins also carry species-specific epitopes, suggesting that their combined use may allow for an increase in sensitivity, which may be especially relevant in conditions of low malaria transmission and/or low density of Anopheles vectors (dry season, post anti-vector control interventions).
The gSG6 salivary protein: a marker of exposure to both Afrotropical and Asian malaria vectors?
Comparison of SG6 proteins in selected malaria vectors
The wide cross-reactivity between the A. gambiae and A. funestus SG6 proteins, along with the observations reported above, supports the idea that the anti-gSG6 IgG response may represent a reliable indicator of exposure to malaria vectors of the subgenus Cellia, at least to members of the Pyretophorus, Myzomyia and Neocellia Series, which share 80% to 84% identity. Therefore, it is likely that the gSG6 protein will also work as marker of exposure to A. stephensi and other Asian malaria vectors. Furthermore, the highly conserved folding and the relatively high identity (61-65%) indicates that anti-gSG6 antibodies are also expected to cross-react with SG6 family members from species of the Anopheles subgenus, although extension of cross-reaction and its potential usefulness would need proper validation.
This study provided solid experimental evidence that the human antibody response to the A. gambiae salivary protein gSG6 represents a reliable indicator of human exposure to the three main malaria vectors in tropical Africa: A. gambiae, A. arabiensis and A. funestus. Such a tool may be very useful for malaria epidemiological studies and for monitoring vector control interventions. The additive effect obtained when the two recombinant proteins are combined also allows for an increase in sensitivity of the assay. Moreover, data reported here also suggest that most likely the gSG6 protein may work as a marker of exposure to A. stephensi and other Asian malaria vectors or, as alternative, that inclusion of SG6 protein from a third species may provide a sensitive marker of human exposure to bites of both African and Asian malaria vectors.
The work was initially supported by the BioMalPar European Network of Excellence (503578) and continued in the framework of the EU-funded EVIMalaR NoE (242095). CR was partly supported by a short term fellowship of Istituto Pasteur-Fondazione Cenci-Bolognetti (Sapienza University, Rome). RR was supported by Fondazione "Compagnia di San Paolo" (Torino) through the Italian Malaria Network and partly by the EU-funded INFRAVEC project (228421).
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