Open Access

Anopheles darlingi (Diptera: Culicidae) displays increased attractiveness to infected individuals with Plasmodium vivax gametocytes

  • Elis PA Batista1,
  • Elizangela FM Costa1 and
  • Alexandre A Silva1, 2Email author
Parasites & Vectors20147:251

https://doi.org/10.1186/1756-3305-7-251

Received: 27 October 2013

Accepted: 20 May 2014

Published: 29 May 2014

Abstract

Background

Most hematophagous insects use host odours as chemical cues. The odour components, some physiological parameters and host attractiveness are affected by several conditions, including infection by parasites, e.g., plasmodia and, therefore, change the epidemiological scenario. This study evaluated the attractiveness of individuals with vivax malaria before, during (7 days) and after treatment (14 days) with specific antimalarial drugs.

Findings

Mosquito attractiveness to vivax-infected patients was assessed using a vertical olfactometer using the foot as a source of body odour. The ratio of Anopheles darlingi mosquitoes in the lower chamber of the olfactometer was used to calculate the attractiveness, and patient temperature was measured using a digital thermometer. An increased attractiveness was found only in patients bearing vivax gametocytes during the first experiment (early infection) (P < 0.001). Patients in the first experiment tended to have a higher body temperature, but grouping patients into fever and non-fever resulted in a higher attractiveness only in the fever group of gametocyte carriers, suggesting a synergistic effect of temperature and gametocytes in the host attractiveness to A. darlingi.

Conclusions

Gametocyte presence and fever in vivax malaria patients increased short distance host attractiveness to An. darlingi.

Keywords

Anopheles darlingi Malaria Olfactometer

Findings

Background

Few ecological relationships are so intimate such as a parasite and its host. Both antagonists, coexisting over time, evolve an “arms race”, i.e. hosts evolve defense mechanisms, including the immune system to prevent, eliminate or even tolerate parasites that develop new ways to find, explore and manipulate their hosts, that can increase their transmission success.

Vector feeding behavior on hosts can be modified by parasites[1], but parasite infection can result in changes to host physiology that increases the detection rate amongst mosquitoes. Moreover, defensive behavior of vertebrates can be reduced when the hosts are sick, reducing awareness to bites or even inability to respond appropriately to the attack[2]. Changes in the attractiveness and body temperature are also affected during infection by parasites[3].

Despite some evidence regarding the attractiveness of An. gambiae to P. falciparum-infected individuals[4], the mechanism and compounds mediating attractiveness to infected hosts has not been described so far. Regardless of the mechanisms employed by the parasite in the manipulation of vector and vertebrate host to increased transmission, the result can make a difference on the epidemiology of the disease and, therefore, the understanding of such mechanisms can be used as a strategy to decrease and/or block parasite transmission. The present work investigated the short distance attractiveness response of the main malaria vector in North Brazil, An. darlingi, to infected patients with Plasmodium vivax, responsible for most of the malaria cases in Brazil.

Methods

This study was approved by the local Ethics Committee (CEP) of the Research Centre of Tropical Medicine of Rondônia (Cepem - RO), protocol number 091/2009.

The behavioral experiments on Anopheles darlingi were performed at the Laboratory of Entomology of the Fundação Oswaldo Cruz (FIOCRUZ-RO) in Porto Velho, Rondonia state, Brazil. Six people completed all the experimental phases and 11 people participated in the first phase. Patients from both sexes, with an age range from 20 to 50 years, diagnosed with vivax malaria with or without gametocytes by blood smear, performed the experiments in a vertical olfactometer[5]. Each experiment was replicated three times using 10 F1An. darlingi females, which were 5 days old and deprived of a sugar meal for 12 hours. A total of 10 minutes for each experiment included five minutes prior to stimulation with no odour or heat sources and five minutes with odour and heat sources, i.e., patient foot under the lower chamber. Mosquitoes were introduced into the upper chamber of the olfactometer and the result was defined by the sum of mosquitoes present in the lower chamber at the end of all replicates.

Before each experiment, the axillary temperature of the volunteers was measured using a digital thermometer. Each subject that completed all the experimental phases performed the same experiments three times; the first was just after diagnosis (before starting treatment), the second after seven days (during treatment) and the third, 14 days after diagnosis (after treatment). During the last experiment, volunteers had completed treatment and recovered their innate attractiveness, i.e., control.

The mosquito attractiveness of patients that completed all the experimental phases, i.e., before, during and after treatment and the presence of different forms of P. vivax were evaluated using Two-Way RM ANOVA and comparisons using Tukey’s test (N = 3). Body temperature of patients throughout the treatment period was evaluated using One Way RM ANOVA (N = 6). Correlation between the body temperature of patients in the first experiment and the number of mosquitoes in the lower chamber of the olfactometer was performed using Pearson correlation. The effect of different forms of P. vivax and body temperature, i.e., fever and gametocytes, fever and no gametocytes, no fever and gametocytes and no fever and no gametocytes in mosquito attractiveness was performed using patients within each combination mentioned and evaluated using Two-Way ANOVA and comparisons using Sidak’s test (N = 2) (Prism 6, GraphPad).

Results

There was a significant interaction between the treatment phase and the presence of gametocytes (F = 15.0, P = 0.0046). The symptomatic patients carrying gametocytes attracted more than twice as many mosquitoes during the infection phase compared with other treatment periods. There were no significant differences in mosquito attractiveness to patients with no detectable gametocytes (P > 0.05) throughout the treatment period. Patients carrying gametocytes attracted 3 times more mosquitoes than patients with no detectable gametocytes only in the infection phase (F = 10.65; P = 0.0056). After 7 and 14 days of treatment, no significant differences in mosquito attractiveness to patients previously infected with different forms of P. vivax was detected, but mosquito number tended to be lower in patients previously bearing gametocytes (Figure 1).The average body temperature of patients tended to be higher during the first experiment, but the differences were not significant (F = 4.67, P = 0.053) (Figure 2), and no correlation between body temperature and attractiveness was found (R = 0.38, P = 0.12).However, grouping patients according to their body temperature (fever, i.e., >37.5°C and no fever, i.e., <37.5°C) and the presence of gametocytes (present and absent) in the first experiment indicated that febrile patients bearing gametocytes were more attractive to mosquitoes (F = 15.4, P = 0.017) (Figure 3).
Figure 1

Anopheles darlingi attractiveness to vivax malaria patients during different periods throughout treatment. Two-Way Anova Repeated Measures and Tukey’s test (comparisons). Different letters indicate significant (P < 0.05) differences in mosquito attractiveness to patients bearing gametocytes during the treatment period. NS indicate non-significant (P > 0.05) differences in mosquito attractiveness to patients with no detectable gametocytes during the treatment period. * indicates a significant (P < 0.01) difference in the mosquito attractiveness between patients with detectable gametocytes (gametocytes) (N = 3) and non-detectable gametocytes (no gametocytes) (N = 3) during the infection phase.

Figure 2

Body temperature of vivax malaria patients during different periods throughout the treatment. One Way RM Anova. N = 6.

Figure 3

Anopheles darlingi attractiveness to symptomatic vivax malaria patients related to body temperature and parasite stages. Gametocyte carriers were defined as patients with detectable sexual stages of the parasite in blood smears using microscopy. Fever = Individuals with body temperature >37.5°C; No Fever = individuals with body temperature <37.5°C. Two-way ANOVA (fever and gametocytes) and Sidak’s test (comparisons). * indicates significant differences (P < 0.05). NS indicates non-significant differences (P > 0.05). N = 2 for each variable combination (i.e., fever and gametocytes, fever and no gametocytes, no fever and gametocytes and no fever and no gametocytes).

Discussion

The vertical olfactometer design allows the interaction of physical and chemical cues at a short distance simultaneously during experiments and was successfully performed with Aedes aegypti[6]. Despite differences in mosquito response, i.e., higher for Ae. aegypti, present data indicate that it is also suitable for experiments with anophelines.

Even with individual innate differences in mosquito attractiveness, the effect of the parasite in the infective stage for the mosquito was significant. In a semi-field condition study conducted in Kenya, Lacroix and colleagues[4] found that children carrying gametocytes attracted twice as many An. gambiae in relation to uninfected children and children infected with asexual forms of Plasmodium, corroborating the results obtained in the present work for short distance attractiveness. In both studies, increased attractiveness was only observed in experiments prior to treatment with antimalarial drugs. Furthermore, Lacroix and colleagues[4] also reported a decrease in attractiveness after the elimination of the parasite.

Unlike in Lacroix’s study[4], uninfected individuals were not tested in the present study, but experiments were performed with the same individuals during and after treatment, when they had recovered their innate attractiveness and we also found no difference in attractiveness in those previously infected with asexual forms and gametocyte carriers after treatment. Although antimalarial drugs include a known gametocidal drug, i.e., primaquine, gametocyte clearance was not confirmed in the present study.

Although in this study patients were all symptomatic individuals, the increased attractiveness did not result from host behavioral changes, but probably from physiological (odour and temperature) changes, since during the experimental procedures, mosquitoes had no contact with patients. Present results suggest that a specific stage of the parasite, i.e., gametocytes, modify the odour profile of the host, colloquially known as “malaria smell”. Interestingly, increased attractiveness to Anopheles gambiae was also reported even in asymptomatic individuals carrying gametocytes[4], prompting their importance as parasite reservoirs, as highlighted by Alves and colleagues[7].

The symptomatic infection probably not only changes the odour profile, but also other important short distance attraction cues such as temperature and humidity. Despite no correlation between temperature and attractiveness in the present work, Eiras & Jepson[6] argued that an increase in temperature in relation to environmental temperature prompted a significant flight response in Aedes aegypti. This indicates that physical stimuli are important for orientation at short distances and should be evaluated along with the chemical cues using different approaches for long distance experiments, e.g., taxis assays[8].

Kelly[9] suggested that the change in the innate attractiveness of an infected person results from a diffuse coevolution of parasite, vector and host, indicating a time of increased vulnerability to the bites. Furthermore, increased attractiveness due to host-infected cues seems to be a convergent strategy for host-seeking vectors, e.g. Lutzomyia longipalpis[10].

This scenario probably has a significant epidemiological impact on the transmission dynamics of malaria in endemic areas such as Africa[11] and the Brazilian Western Amazon[12] with a high number of asymptomatic carriers of gametocytes. Moreover, Katsuragawa et al.[13] studied the dynamics of malaria transmission of an endemic area in Porto Velho, Rondonia and argued that the concentration of malaria cases in some residences might also be a result of a higher frequency of “fever episodes” and therefore increased sweat production by inhabitants of these houses resulting in increased mosquito attraction.

Conclusions

The use of the vertical olfactometer for studying short distance attractiveness responses to malaria patients was successfully performed with An. darlingi and suggests that it is suitable for assays with different mosquito species.

Malaria infection affected the short distance attractiveness of the mosquito An. darlingi only in patients carrying gametocytes. Fever was also important to increase host attractiveness.

Since the increased attractiveness for hosts carrying gametocytes may be mediated by olfactory signals, as yet unidentified, studies describing the physiological changes caused by infection are needed to elucidate the factors related to attractiveness.

Declarations

Acknowledgements

We are grateful to all volunteers that participated in the experiments and to the Fiocruz-RO for logistical support and to the laboratory staff during mosquito rearing. We are also grateful to Alvaro Eduardo Eiras, UFMG for providing the vertical olfactometer and for his comments about the manuscript. The study was supported by CAPES. We also thank Amy Nicole Grabner (CEBIO, FIOCRUZ/UNIR) for the English revision of the manuscript.

Authors’ Affiliations

(1)
Departamento de Biologia, Laboratório de Bioecologia de Insetos, Núcleo de Ciência e Tecnologia da Universidade Federal de Rondônia
(2)
Laboratório de Entomologia, Fundação Oswaldo Cruz – Rondônia

References

  1. Koella JC, Sorensen FL, Anderson R: The malaria parasite Plasmodium falciparum increases the frequency of multiple feeding of its mosquito vector Anopheles gambiae. Proc R Soc Lond B Biol Sci. 1998, 265: 763-768. 10.1098/rspb.1998.0358.View ArticleGoogle Scholar
  2. Day JF, Edman JD: Malaria Renders Mice Susceptible to Mosquito Feeding When Gametocytes Are Most Infective. J Parasitol. 1983, 69 (1): 163-170. 10.2307/3281292.View ArticlePubMedGoogle Scholar
  3. Clements NA: The biology of mosquitoes: Sensory reception and behaviour. 1999, London: Cabi PublishingGoogle Scholar
  4. Lacroix R, Mukabana WR, Gouagna LC, Koella JC: Malaria Infection increases attractiveness of humans to mosquitoes. Plos Biol. 2005, 3 (9): 1590-1593.View ArticleGoogle Scholar
  5. Feinsod FM, Spielman A: An olfactometer for measuring host-seeking behavior of female Aedes aegypii (Diptera; Culicidae). J Med Entomol. 1979, 15: 282-285.View ArticleGoogle Scholar
  6. Eiras AE, Jepson PC: Responses of female Aedes aegypti (Diptera: Culicidae) to host odours and convection currents using an olfactometer bioassay. Bull Entomol Res. 1994, 84: 207-211. 10.1017/S0007485300039705.View ArticleGoogle Scholar
  7. Alves FP, Gil LHS, Marrelli MT, Ribolla PEM, Camargo EP, Pereira-Da-Silva LH: Asymptomatic carriers of Plasmodium spp. as infection source for malaria vector mosquitoes in the Brazilian Amazon. J Med Entomol. 2005, 42: 777-779. 10.1603/0022-2585(2005)042[0777:ACOPSA]2.0.CO;2.View ArticlePubMedGoogle Scholar
  8. Lorenz LM, Keane A, Moore JD, Munk CJ, Seeholzer L, Mseka A, Simfukwe E, Ligamba J, Turner EL Biswaro LR, Okumu FO, Killeen GF, Mukabana WR, Moore SJ: Taxis assays measure directional movement of mosquitoes to olfactory cues. Parasit Vectors. 2013, 6: 131-10.1186/1756-3305-6-131.PubMed CentralView ArticlePubMedGoogle Scholar
  9. Kelly DW: Why are some people bitten more than others?. Trends Parasitol. 2001, 17: 578-581. 10.1016/S1471-4922(01)02116-X.View ArticlePubMedGoogle Scholar
  10. O’shea B, Rebollar-Tellez E, Ward RD, Hamilton JGC, Naiem DE, Polwart P: Enhanced sandfly attraction to Leishmania-infected hosts. Trans R Soc Trop Med Hyg. 2002, 96: 117-118. 10.1016/S0035-9203(02)90273-7.View ArticlePubMedGoogle Scholar
  11. Rey L: Parasitologia. 2008, Rio de Janeiro: Guanabara KooganGoogle Scholar
  12. Tada MS, Ferreira RGM, Katsuragawa TH, Dalla Martha RC, Costa JDN, Albrecht L, Wunderlich G, Pereira-Da S: Asymptomatic infection with Plasmodium falciparum and Plasmodium vivax in the Brazilian Amazon Basin: to treat or not to treat?. Mem Inst Oswaldo Cruz. 2012, 107 (5): 621-629. 10.1590/S0074-02762012000500008.View ArticlePubMedGoogle Scholar
  13. Katsuragawa TH, Gil LHS, Tada MS, Silva AAE, Costa JDN, Araújo MS, Escobar AL, Pereira-Da-Silva LH: The Dynamics of Transmission and Spatial Distribution of Malaria in Riverside Areas of Porto Velho, Rondônia, in the Amazon Region of Brazil. PLoS One. 2010, 5 (2): 1-12.View ArticleGoogle Scholar

Copyright

© Batista et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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