Transcription in mosquito hemocytes in response to pathogen exposure
© BioMed Central Ltd 2009
Published: 5 June 2009
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© BioMed Central Ltd 2009
Published: 5 June 2009
Mosquito hemocytes are blood cells that are fundamental for combating systemic infection. A study published in BMC Genomics shows that hemocyte gene transcription in response to immune challenge is pathogen-specific and reaffirms the primary role of these cells in immunity.
Throughout their lifetime, mosquitoes are in danger of acquiring deadly pathogens. During their egg, larval and pupal stages, mosquitoes live in aquatic environments that are often rife with bacteria. Culex pipiens, for instance, thrive in sewer systems. As adults, mosquitoes often lose their legs, creating openings by which pathogens can enter their body. Female mosquitoes also engage in the dangerous behavior of biting vertebrates and ingesting their blood. This is done to acquire the nutrients necessary for the production of large numbers of eggs, but it exposes mosquitoes to blood-borne pathogens, such as Plasmodium, filarial nematodes and arboviruses. Besides being deadly and debilitating to humans, these organisms are pathogenic to mosquitoes if acquired in high enough numbers.
So how does a mosquito respond to a microbial pathogen? When a foreign invader enters the body cavity of a mosquito it elicits a systemic immune response. Similarly to that of vertebrates, this immune response has both humoral and cellular components. However, the invertebrate response lacks the properties of somatic hypermutation and immune memory that are hallmarks of vertebrate adaptive immunity. The mosquito cellular immune response includes phagocytosis and encapsulation by hemocytes (blood cells). The humoral response includes the phenoloxidase cascade system of melanization (an enzymatic process in which melanin polymers cross-link with proteins, sequestering pathogens and closing wounds), inducible antimicrobial peptides, reactive oxygen and nitrogen intermediates, and pattern recognition molecules. As with vertebrates, the line between cellular and humoral immunity is blurred because many humoral components are produced by hemocytes. Because of their involvement in both cellular and humoral pathways, the circulating nature of these cells and their ability to respond rapidly to an infection, it is now clear that hemocytes are the first line of defense against microbes that enter the hemocoel (body cavity) of the mosquito .
Given their fundamental role in immunity, it is surprising that little is known about the biology of mosquito hemocytes. This is probably because they are few in number and are difficult to manipulate. Much of what we know comes from studies that have morphologically and functionally characterized hemocyte subpopulations and described their role in pathogen killing and sequestration [2, 3]. Other studies have focused on the discovery and characterization of individual genes and proteins, enabling in-depth investigations of a limited number of targets that were initially identified because of homology to genes with known function in other organisms . However, a considerable percentage of the mosquito genes that have been identified either bioinformatically or through expressed sequence tag (EST) projects are of unknown function. Because single-gene approaches are unlikely to focus on these unknowns (many of which may be crucial), whole-genome transcriptomic and proteomic analyses are needed to narrow the field.
Recent studies have begun to exploit mosquito genomic data to screen thousands of genes simultaneously for transcriptional changes after various treatments. Initial work on mosquito hemocytes has included the characterization of transcriptional changes in hemocytes from the mosquito Armigeres subalbatus following infection with the filarial nematode Brugia malayi and in hemocytes from the mosquito Aedes aegypti following infection with live bacteria [5, 6]. Clearly, additional work is needed in other medically important vectors to identify genes that are regulated in response to infection.
Mosquitoes mount strong phagocytic immune responses against E. coli, whereas sequestration of M. luteus is primarily by melanization . Plasmodium ookinetes (the motile zygotes of the parasite) in the midgut are killed by either lysis or melanization within 48 hours of infection . In contrast, Plasmodium sporozoites (the infective stage) migrating through the hemocoel during the third week after infection are killed by mechanisms that have not been firmly characterized. However, the low levels of phagocytosis and melanization observed during migration suggest that most parasites are killed by some form of lytic mechanism .
These differences in the immune responses mounted against different pathogens are in agreement with the data presented by Baton et al. , which reveal distinct transcriptional signatures against two different bacterial species and between two stages of malaria parasites. After Plasmodium berghei infection, a total of 431 genes were differentially expressed in hemocytes. However, only 5.3% of the genes differentially expressed during Plasmodium infection were regulated in a similar manner for both the ookinete and sporozoite stages, whereas 3.7% of genes were regulated in opposite directions, indicating that more than 90% of genes were regulated exclusively during one of the two infection stages assayed. Genes involved in melanization were induced during ookinete invasion but not during sporozoite migration, consistent with previous reports that ookinetes often become melanized but that this rarely happens to sporozoites [4, 9]. Interestingly, 37.2% of the immune genes regulated during sporozoite migration were members of the fibrinogen-related protein family (FREPs; also known as FBNs) of mosquitoes. This family is made up of 59 genes in A. gambiae, an expansion from the 14 genes found in Drosophila . FBNs in Anopheles and other mosquitoes have been shown to be involved in antibacterial and anti-Plasmodium immunity, and it is tempting to speculate that their expansion was a consequence of continuous exposure to blood-borne pathogens.
After challenge with heat-killed E. coli or M. luteus, 641 transcripts were differentially regulated in hemocytes, but only 6.9% of those transcripts were similarly regulated in the two groups . This was due mainly to a weaker response in transcriptional regulation following E. coli challenge, as M. luteus altered the transcriptional state of almost four times as many genes as E. coli. When only genes with putative immune function were analyzed, 7.7% of genes were differentially regulated in a similar manner. E. coli and M. luteus both induced genes involved in melanization, even though the latter pathogen was visually observed to elicit this immune process at a considerably higher rate. In addition, transcripts of genes involved in phagocytosis either decreased in abundance or were not regulated following immune challenge with E. coli, whereas transcription of several genes involved in this immune process increased in abundance after exposure to M. luteus, seemingly in conflict with the observation that phagocytic events are much more common against E. coli than M. luteus. It is probable that this is the result of different molecular interactions during the internalization of the two pathogens, including the possible requirement of melanization of M. luteus before the onset of phagocytosis .
Overall, the data presented by Baton et al.  are mostly consistent with previous transcriptomic analyses of the hemocytes of other mosquito species [5, 6], with the exception of the level of immune induction in A. gambiae hemocytes following challenge with heat-killed E. coli. Possible reasons for these discrepancies include mosquito species-specific differences or that inoculation with dead bacteria elicits a weaker response than infection with living bacteria. Furthermore, given that the rodent malaria parasite Plasmodium berghei and the human malaria parasite Plasmodium falciparum elicit different midgut and carcass transcriptional profiles in response to ookinete invasion , future studies will need to address whether the hemocyte response now being reported  is similar to the response that occurs during infection with human malaria parasites. Nevertheless, the data presented by Baton et al.  provide a comprehensive dataset that will serve as a starting point for the functional characterization of numerous mosquito genes. The report of the breadth of genes transcribed by hemocytes, together with data on their cellular biology, supports the hypothesis that they form the primary component of the mosquito immune response [1–3, 7].
Plasmodium parasites, the causative agents of malaria, kill over a million people per year, and another 500 million people suffer from clinical disease. Currently, the control of mosquito-borne diseases has consisted of treating infected individuals, killing the mosquito vector and limiting vector-human contact. Although these approaches have reduced disease prevalence, their efficacy is diminishing, mainly because of the emergence of drug resistance by Plasmodium parasites and insecticide resistance in the insect vector. Thus, because of the reduced efficacy of current control methods, compounded by the failure to discover new drugs, insecticide replacements and effective vaccines, it has become necessary to develop new control strategies.
One possible strategy that has gained support in recent years is to genetically manipulate insect pests such that they are unable to transmit disease-causing pathogens, and to mass release them into the environment to displace natural populations of susceptible mosquitoes. Before such a strategy can be implemented several hurdles must be overcome, one of which is the identification of candidate mosquito genes that confer resistance to infection. The best candidate genes are probably transcribed in hemocytes, because these cells are involved in immune responses throughout the insect and even produce proteins with anti-parasitic activity in the midgut . The study by Baton et al.  provides a comprehensive dataset of gene transcription following Plasmodium infection and sets the stage for in-depth functional studies on the role of candidate genes in fighting infection.
The author is funded by NSF grant IOS-0817644.