Background
Plasmodium falciparum is a highly polymorphic parasite with a high antigens heterogeneity [
1]. This heterogeneity may represent a major obstacle to the development of an effective vaccine [
2].
In general, the
P. falciparum infections include a complex mixture of biologically and genetically different populations, as has been demonstrated by different techniques, including the Restriction Fragment Length Polymorphism (RFLP) [
3] and the Polymerase Chain Reaction (PCR) [
4]. PCR has been used to study the existing polymorphisms in various markers, such as the Merozoite Surface Proteins 1 (MSP-1) and 2 (MSP-2), the circumsporozoite protein (CSP) and the glutamate-rich protein (GLURP) [
5]. Various studies indicate that the genetic diversity in a specific area is related to the level of transmission [
5,
6]. Therefore, a high prevalence of infection multiplicity has been detected in hyper- and holoendemic zones [
7], compared to low transmission zones [
8]. Only a number of basal or identical genotypes has been found in low transmission areas, such as Brazil [
9] and Honduras [
4]. The basis of the genetic diversity is the recombination that occurs in the sexual phase of the parasite within the mosquito. According to this, the higher the transmission, the greater the recombination frequency [
10]. However, some authors indicate that the transmission level would not be the only cause for genotype variability [
11].
In a study conducted at three locations on the Island of Bioko (Equatorial Guinea), a high allelic diversity has been observed in the
P. falciparum populations, particularly in the location with the greatest geographical isolation [
12]. Furthermore, a correlation was also noted in this study between the parasitaemia levels, age and multiplicity of infection (MOI).
The Annobon population lives in a highly isolated situation, given the distance that separates the island from Bioko and the mainland of Equatorial Guinea. Not much information exists about the transmission of malaria on Annobon. The first known epidemiological and transmission survey dates back to 1987 [
13]. During that year, a seroparasitologic study had been conducted among 185 children between two and nine years of age. The crude parasite rate (CPR) was 55.1% and the splenic index of 54.6%. Four years later, another survey was conducted during the dry season, when samples were taken from 1,326 individuals from all age groups, 263 of whom were under five years old. The CPR of children between two to nine years of age was 68%, and 74% in children below five years of age (non published data). In 1993, during the rainy season, the study was focused on 300 children under five years of age. The CPR was 76% in that age group. The parasite density index was 5.8 [
14].
No data is available regarding the transmission, even though taking into account the studies conducted on the island of Bioko [
15] and on the neighbouring islands of Sao Tomé and Principe [
16,
17], the malaria vector in Annobon is expected to be
Anopheles gambiae sensu lato (s.l.).
In 2004 two transversal studies (dry and rainy season) were conducted in order to establish the basics for a control campaign 1) establish the malaria transmission pattern on Annobon, and 2) analyse the circulating P. falciparum allelic forms. Finally, a possible eradication of malaria on the island is discussed.
Results
The molecular diagnostics was performed on all the blood samples collected in order to assess the quality and reliability of the microscopic diagnostics. In both surveys, the sensitivity and specificity of microscopic diagnostic were high (above 70% in all cases).
In June 2004 (dry season), a total of 112 children under 9 (60 male and 52 females) were surveyed. The mean age for the males was 3.7 (SD = 2.3) years and 3.2 (SD = 2.4) years in the case of the females (t-test, p = 0.298). In December (rainy season), 83 children (46 males and 37 females) were surveyed. In the same way as in the first survey, there were no significant differences in the mean age of males and females (t-test, p = 0.315), 3.8 (SD = 2.6) and 4.4 (SD = 2.7) years, respectively.
The CPR was 17% (19/112) [Confidence Interval 95%: [10%–24%] in the dry season and 60% (50/83) [CI: 49%–71%] in the rainy season. In the first survey, prevalence of infection was significantly higher among males than females (Fisher chi-squared, p = 0.005). This difference was not noted in the second survey (Pearson chi-squared, p = 0.561) (Table
1).
Table 1
Crude Parasite Rate and bed nets use by age groups and sex for season
≤ de 1 year
|
29
| 3 | (0–10) | 90 | (73–98) |
21
| 43‡ | (21–64) | 86 | (64–97) |
1–5 years
|
57
| 19 | (9–30) | 85 | (73–94) |
28
| 54‡ | (35–72) | 89 | (71–98) |
5–9 years
|
26
| 27 | (10–44) | 76 | (55–91) |
34
| 76‡ | (62–91) | 75 | (57–89) |
Male
|
60
| 27‡ | (15–38) | 77 | (66–88) |
46
| 63 | (49–77) | 73 | (59–86) |
Female
|
52
| 6‡ | (0–12) | 92 | (85–100) |
37
| 57 | (40–73) | 94 | (87–100) |
No Bed net #
|
17
| 24 | (3–44) | | |
14
| 86‡ | (67–100) | | |
Bed net
|
92
| 14 | (7–21) | | |
66
| 53‡ | (41–65) | | |
In addition, the CPR was higher in the 5–9 year age group in the two seasons, although the difference with respect to the other age groups was only significant in the rainy season (Pearson chi-squared, p = 0.031).
In Equatorial Guinea, four species of human
Plasmodium have been described, although infections by
Plasmodium vivax are anecdotical [
18]. The main species observed in all the infections was
P. falciparum, 96% (66/69). The mixed infections (
P. falciparum/
Plasmodium malariae) diagnosed by microscopy in three percent of infections were not confirmed by PCR. The gametocytic index (percentage of studied population with gametocytes in blood) was 6% (7/112) during the dry and 14% (12/83) in the rainy season.
The percentage of children sleeping under a bed net was over 80% in the two surveys. Furthermore, the number of girls that claimed to sleep under a bed net was significantly higher than the number of boys, both in dry (Fisher chi-squared, p = 0.036) and rainy season (Fisher chi-squared, p = 0.016). Children aged between five and nine were less protected by a bed net, although the difference with respect to the rest of the groups was not significant (Fisher chi-squared, p = 0.396 in the rainy, Fisher chi-square, p = 0.397 in the dry) (Table
1). Data was collected regarding the state and use of the bed nets by the children surveyed.
The prevalence of anaemia during the rainy season is significantly higher than that observed during the dry season (Fisher chi-square, p < 0.001). In the study conducted during the dry season, only 3.1% (3/98) of the children surveyed had a PCV percentage less or equal to 30%. PCV percentage could not be measured in 14 cases. With such a low sample size, the relation between the anaemia and the rest of the measured variables (CPR, use of bed nets, gender and age) could not be analysed. However, during the rainy season, 33.3% of the children surveyed (26/78) were anaemic at the time of the study. PCV percentage could not be measured in five cases.
Table
2 shows the odds ratio for the different measurements with respect to the anaemia. No association was found between the CPR, the use of bed nets and gender, with anaemia. However, significant differences were found between the different age groups (p = 0.016). Children between five and nine years of age were five times less at risk of being anaemic than those below one year of age.
Table 2
Feasible factors for suffering from anaemia in the rainy season
|
Males
| 46 | 1 | - | |
Sex
|
Females
| 37 | 0.7 | 0.2–2.2 | 0.542 |
|
under 1 year
| 21 | 1 | - | - |
|
1 to 5 years
| 28 | 0.7 | 0.2–2.5 | 0.615 |
Age
|
*5 to 9 years
|
34
|
0.2
|
0.04–0.7
|
0.016
|
Sleeps under net #
|
No
| 14 | 1 | - | - |
|
Yes
| 66 | 0.9 | 0.2–4.1 | 0.888 |
CPR
|
No
| 33 | 1 | - | - |
|
Yes
| 50 | 1.2 | 0.4–3.5 | 0.738 |
A total of 28 populations of the three allelic families of the
msp-1 gene were identified and 39 of the
msp-2 gene. Out of these, 17 for the
msp-1 gene and nine for the
msp-2 gene were present in the two climatic seasons. Fifty-seven per cent of the MAD20 allelic families of the msp-1 gene were only present in the samples gather during the dry season and 66.7% of those of the
msp-2 gene only in the rainy season. The only allelic form belonging to the RO33 family of the
msp-1 gene was observed in the two surveys (Table
3).
Table 3
Circulating P. falciparum population diversity for the msp-1 and msp-2 genes
Total Populations
| 1 | | 20 | | 7 | | 39 | |
Common populations
| 1 |
100.0%
| 14 |
70.0%
| 2 |
28.6%
| 9 |
23.1%
|
Only dry populations
| 0 | 0.0% | 1 | 5.0% | 4 | 57.1% | 4 | 10.3% |
Only rainy populations
| 0 | 0.0% | 5 | 25.0% | 1 | 14.3% | 26 | 66.7% |
The variability of circulating allelic populations is significantly higher in the rainy than the dry season (Pearson chi-squared, p = 0.03). During the dry season, the number of msp-1 gene allelic populations is similar to that registered in the rainy season (22/23), while in the case of the msp-2 gene this number nearly triples (13/35).
The multiplicity of infections (MOI) is similar during the dry and rainy season (t-test, p = 0.3670), the MOI average for the dry season is 2.2 (SD = 1.3), while it is 1.9 (SD = 1.0) for the rainy season.
In the case of the samples taken during the rainy season, no association was observed between age, gender, use of bed nets and anaemia, and MOI values over 1. The number of P. falciparum positive samples in the dry season was insufficient to carry out this type of analysis.
Discussion
The transmission of malaria on the Island of Annobon is stable although mainly occurs during the rainy period. The number of diagnosed malaria cases between 2002 and 2003, in the unique health center of the island (the provincial hospital), was 660 (314 per thousand inhabitants) in the dry season and 1,370 (651 per thousand inhabitants) in the rainy season.
Taking into account the results obtained in the transversal studies and the regional hospital registry, it could be hypothesized about a seasonal malaria transmission in the island. This markedly seasonal transmission pattern had not been observed in previous studies [
13,
14], nor on the neighbouring islands of São Tomé and Príncipe [
21], but had been reported in Gabon [
22]. During a study conducted in two locations in south-west Gabon, a transmission peak was noted during the rainy period and
A. gambiae s.l was identified as the malaria vector. It is necessary to perform an entomological longitudinal study on Annobon to identify the main malaria vector to verify the transmission pattern.
In Annobon, a significant difference was observed in the prevalence of infection between sexes (males more than females) during the dry season. Furthermore, the prevalence of infection was higher in children between five and nine years old, but only during the rainy season. The CPR difference between sexes was not observed in studies conducted in other regions of the country, on the island of Bioko [
14,
23] and mainland region [
14], even though differences have been detected between age groups.
The only malaria prevention strategy in Annobon is currently the use of insecticide-treated bed net. There are no distribution and reimpregnation points on the island, which means that all the bed nets come from the country's capital, Malabo. Despite this, the cover reached on the island is high (80% of the children surveyed said that they slept under a bed net), although some differences were noted between sexes (females more than males) and age groups (five to nine years old less than other age groups). This would neither explain the differences found in the prevalence of infection, nor the reason for the seasonal differences. However, it is possible that the sample size calculated to dry season was insufficient to established differences between groups, because of the low CPR found in this season against preliminary data [
13].
On the other hand, the percentage of children surveyed with anaemia was significantly higher in the greater transmission period (rainy season). No seasonal differences in the prevalence of anaemia were observed in Bioko, nor were any associations found with variables such as the sex, age, place of residence and use of the bed net [
23]. On Annobon, the risk of suffering from anaemia during the rainy season is five times lower in children between five and nine years of age, despite that age group having the greatest infection prevalence. It is known that, in areas of intense transmission, the development of a certain level of immunity due to the frequent contact with the parasite reduces the risk of anaemia and other severe malaria clinical presentations.
With respect to the analysis of the P. falciparum population variability, seasonal differences in the variety of circulating populations were observed. When analysing this difference in depth, it was observed that the majority of allelic forms of the RO33 and K1 families of the msp-1 gene are present in the two climatic seasons. However, only one third of the allelic forms of the MAD20 family (msp-1 gen) and 23% of the allelic forms of the msp-2 gene were present in the samples collected in both seasons. Therefore, it must be attributed the greater seasonal variability to the alleles of the msp-2 gene. The multiplicity of infection is high and similar in the two seasons and it is not associated with age, sex, the use of the bed net or suffering from anaemia.
In other regions of Africa with a markedly seasonal transmission, such as is the case in Sudan, it has been observed that the diversity of genotypes and multiplicity of infection reduces significantly with the transmission [
24]. In the contrary, in Benín, a country where the transmission is perennial, the decrease in transmission does not have a substantial influence on the diversity of
msp-2 alleles or on the multiplicity of infection [
25]. In a recent study conducted in Guadalcanal (Solomon Islands) [
26], where the malaria transmission is intense and perennial, with a marked peak in the rainy season, no seasonal changes were observed in the variability of
msp-1 gene populations. Furthermore, it was discovered that the allelic variability on these islands was lower than that observed in others countries with a lower transmission level.
Few studies performed to determine the seasonal differences in the allelic diversity of the
msp-2 gene in island zones are available. During a study conducted on São Tomé Island, up to 43
msp-2 alleles were identified, although the variability between climatic seasons was not analysed [
27].
In the study conducted on Annobon, the influence of transmission intensity on the variability of the circulating parasite populations has been suggested, particularly for the msp-2 gene allelic families.
It is known that the genetic recombination occurs during the sexual phase of the biological cycle of the parasite, therefore one of the factors to be taken into account will be the infection rate in the vector. In Equatorial Guinea, the low anopheline density, compared to neighbouring countries [
16], is offset by a high infection rate, close to 20% for some anopheline species in the mainland region [
15,
28]. These high infection rates would increase the number of possible sexual recombinations within the mosquito and, therefore, would favour the circulation of a greater variety of allelic forms, which it could be explained the high variability of the
msp-2 gene observed in rainy season.
In this way, it is logical to think that the introduction of efficient control measures would result in a reduction in the population heterogeneity of the parasite. In Annobon, 80% of the children studied said that they slept under a bed net. This high cover contrasts with the prevalence of infection and the differences found in terms of gender and age groups. On the other hand, no association was found between the risk of being anaemic and whether or not a bed net was used, which contradict the results obtained in other African countries [
29], even for lower cover levels. The high heterogeneity of
P. falciparum allelic forms on the island, may suggest that the impact of bed net usage on transmission is low.
This low protective efficiency of the bed nets may be due to biting habits of the vector species that are not compatible with this measure of protection, and poor state-of-repair and/or inappropriate use of the bed nets by the population. These are important aspects that must be studied in the future to learn more about the malaria transmission mechanisms on the island.
With respect to the P. falciparum allelic diversity in Annobon, it is conceivable that the lack of efficient control measures, a high entomological inoculation rates and crowded households could be related to this high allelic diversity.
Conclusion
During the second half of the last century, it was believed that malaria could be eradicated. Good results were obtained in controlling the transmission of the disease in some regions of Asia, South America and Central America and on some African islands (Sao Tomé and Príncipe), and its eradication in the majority of the countries of the Mediterranean basin [
30]. On the islands of Sao Tomé and Príncipe, the prevalence of the malaria was reduced to 0.95% in 1982 spraying the dwellings with DDT and wide-scale treatment of the population with chloroquine. Disruption of the campaign and spread of choloroquine-resistant
P. falciparum resulted in a serious epidemic with many deaths [
31]. In 1999, a cross-sectional malariological survey carried out in Príncipe suggested that a good clinical management of malaria cases and the use of preventive measures against mosquitoes bites can probably eliminate endemic malaria [
21].
The most recent experience to control and eradicate malaria was in Vanuatu, an island complex in the south-west Pacífic [
32]. In 1991, a campaign was set up in Vanuatu, based on the use of bed nets impregnated with permethrin, widespread treatment of the population during a nine-week period and the use of larvivorous fish. After nine years of monitoring the malariometric indicators and controlling for imported malaria, the disease is considered to have been eliminated from some islands in this region of the Pacific.
Taking this experience into account, the high degree of geographical isolation of the Annobon population and the suggested seasonal nature of the transmission, it is conceivable that malaria could be eradicated in this small African island, as long as the sustainability of the malaria control programme can be ensured.
Authors' contributions
JC was involved in the design of the survey, participated in the data collection and the interpretation of statistical analysis, and coordinated the draft of the manuscript. PB was involved in the molecular studies and helped to draft the manuscript. AL was involved in the molecular analysis. MD was performed the statistical analysis and interpretation, and drafted the manuscript. SN, LB, MO and JB participated in the collection of the data and blood samples. AB and GN participated in the design of the surveys and have given approval of the version to be published. All authors read and approved the final manuscript.