Mosquito survey in Mauritania: Detection of Rift Valley fever virus and dengue virus and the determination of feeding patterns

In Mauritania, several mosquito-borne viruses have been reported that can cause devastating diseases in animals and humans. However, monitoring data on their occurrence and local distribution are limited. Rift Valley fever virus (RVFV) is an arthropod-borne virus that causes major outbreaks throughout the African continent and the Arabian Peninsula. The first Rift Valley fever (RVF) epidemic in Mauritania occurred in 1987 and since then the country has been affected by recurrent outbreaks of the disease. To gain information on the occurrence of RVFV as well as other mosquito-borne viruses and their vectors in Mauritania, we collected and examined 4,950 mosquitoes, belonging to four genera and 14 species. The mosquitoes were captured during 2018 in the capital Nouakchott and in southern parts of Mauritania. Evidence of RVFV was found in a mosquito pool of female Anopheles pharoensis mosquitoes collected in December on a farm near the Senegal River. At that time, 37.5% of 16 tested Montbéliarde cattle on the farm showed RVFV-specific IgM antibodies. Additionally, we detected IgM antibodies in 10.7% of 28 indigenous cattle that had been sampled on the same farm one month earlier. To obtain information on potential RVFV reservoir hosts, blood meals of captured engorged mosquitoes were analyzed. The mosquitoes mainly fed on humans (urban areas) and cattle (rural areas), but also on small ruminants, donkeys, cats, dogs and straw-colored fruit bats. Results of this study demonstrate the circulation of RVFV in Mauritania and thus the need for further research to investigate the distribution of the virus and its vectors. Furthermore, factors that may contribute to its maintenance should be analyzed more closely. In addition, two mosquito pools containing Aedes aegypti and Culex quinquefasciatus mosquitoes showed evidence of dengue virus (DENV) 2 circulation in the city of Rosso. Further studies are therefore needed to also examine DENV circulation in Mauritania.

outbreak [10]. Thereafter, the country has been affected by recurrent RVF outbreaks threatening the population and its essential livestock [11,12]. The occurrence of more than ten of the mosquito species believed to play a role in RVFV ecology has been described in Mauritania over the past 20 years [8,12]. During outbreaks in 1998 and 2003, Culex poicilipes and Culex antennatus mosquitoes were found to be infected with RVFV [13,14]. Additionally, the virus was isolated from Cx. poicilipes during an inter-epidemic period [15]. Together with the evidence of RVFV infection found in cattle, this demonstrates an active circulation of the virus during the absence of reported epidemics [16]. However, only scarce information on the abundance of RVFV-transmitting mosquitoes within Mauritania exist [12], and data on RVFV maintenance during the enzootic cycle are limited [1].
In addition to RVFV, various other mosquito-borne viruses such as Ngari virus (Orthobunyavirus), Wesselsbron virus (Flavivirus), yellow fever virus (Flavivirus) or dengue virus (Flavivirus), responsible for devastating diseases in livestock and/or humans, are occurring in Mauritania [15,17,18]. With estimated 390 million infections per year, dengue fever is the most frequent arboviral disease in humans worldwide. Although the virus is endemic in most tropical and sub-tropical regions of the world, its importance in Mauritania and other African countries may be largely underestimated [19,20]. Serotypes of dengue virus (DENV) have been isolated from humans, mosquitoes and monkeys in Mauritania's neighboring countries Senegal and Mali [21,22,23,24]. However, dengue fever has only recently been reported in Mauritania [12,25] and there is a lack of available data on the circulation of the virus in the country. Moreover, many other arboviruses are probably neglected due to the symptomatic similarities of the diseases and poor surveillance [11,20].
In this study, sampling and analyses of mosquitoes were performed to obtain information on the occurrence and distribution of RVFV and its vectors in Mauritania. To elucidate factors that may favor the maintenance of RVFV during inter-epidemic periods, mosquitoes were sampled in 2018 mainly in the absence of RVF, but also during an epizootic on a farm in southern Mauritania. Captured engorged mosquitoes were additionally examined by blood meal analysis to identify preferred hosts of the mosquitoes and thus a potential RVFV reservoir. Furthermore, we aimed to gain insights into the distribution and circulation of other important arboviruses within mosquito populations in Mauritania. Therefore, mosquito samples were also analyzed for evidence of flavi-and orthobunyaviruses.

II.I. Ethics statement
The collection of blood samples was carried out by the Mauritanian State Veterinary Laboratory, the Office National de Recherches et de Développement de l'Elevage (ONARDEL), in compliance with all relevant national and international regulations and fundamental ethical principles for diagnostic purposes, within the framework of a governmental animal health surveillance program (Ministère de Développement Rural).

II.II. Collection sites
In the course of 2018, mosquitoes were collected in Mauritania. The largest part of the West African country is characterized by the arid desert landscape of the Sahara. Only in the southern regions of Mauritania, where the Senegal River marks the border with Senegal, a more humid climate (semi-arid climate of the Sahel) prevails [12], favoring the occurrence of high mosquito densities. Therefore, in this study mosquitoes were collected in three southern regions of Mauritania: in Nouakchott, the capital and its surroundings (four locations: Socogim Le Ksar; Botanical Garden Sebkha; Basra Sebkha; Arafat); in Trarza (three locations: Rosso, in and outside the city; Keurmacen); and in Hodh El Gharbi (one location: Tintane) (Fig 1). In December 2018, during the rainy season, symptoms indicative for RVF were observed on a cattle farm in Rosso, which is why the farm was selected as sampling site. Altogether, mosquito traps were set at eight different dates at eight different locations. In Nouakchott, the traps were set twice at two of the locations (Socogim Le Ksar and the Botanical Garden in Sebkha). Thus, samples were taken at a total of ten different sampling sites, differing in date and/or location.

II.III. Mosquito collection and species identification
Mosquitoes were collected with Heavy Duty EVS (Encephalitis Vector Survey) CO 2 Mosquito Traps (BioQuip Products Inc., Rancho Dominguez, CA, USA). Carbon dioxide (CO 2 ) filled bottles were placed next to traps and CO 2 was directed to the traps with hoses to attract mosquitoes. The traps were set up at dusk in sheltered places and run over night. At dawn, bags with captured mosquitoes were gathered and subsequently transferred to -20˚C. Frozen mosquitoes were placed on chill tables and morphologically identified to species (or genus) levels using taxonomic keys by Peter F. Mattingly and Assane G. Fall [26,27]. Male mosquitoes were identified to genus level only. After identification, mosquitoes were stored at -80˚C in pools of up to ten mosquitoes of the same species/genus, sex and sampling site. Blood-fed mosquitoes (with a visible blood meal in the abdomen) were separated and stored individually. For pathogen examination, cooled samples were shipped to the Friedrich-Loeffler-Institut (FLI). At FLI, samples were stored at -80˚C until further processing.

II.IV. Serum collection
As mentioned above (II.II.), in December 2018, Montbéliarde cattle on a farm situated 15 km south of the town of Rosso (Fig 1), near the Senegal River, showed clinical symptoms indicative of RVFV infection. To confirm the clinically observed RVF disease, sera were taken from 16 individuals of the herd. In addition, in order to gain further insight into the onset of this epizootic, 28 sera from indigenous cattle on the same farm that had been collected during a routine medical examination one month earlier were analyzed. For protection of cattle and humans, animals were carefully captured and restrained during blood collection.

II.V. RNA/DNA extraction
Three 3-mm steel beads and 500 μl (mosquito pools) or 300 μl (individual mosquitoes) Minimal Essential Medium (MEM) with penicillin, streptomycin, amphotericin and gentamicin were added to the samples. Mosquitoes were homogenized using a TissueLyser II (Qiagen, Hilden, Germany) at 30 Hz for 2 minutes, and then centrifuged at 4˚C, 13,000 rpm for 3 minutes. Supernatants were used for RNA/DNA extraction with the NucleoMag VET kit (MACHER-EY-NAGEL GmbH & Co. KG, Düren, Germany) according to the manufacturer's recommendations. Residues of the supernatants were stored at -80˚C. Before conducting the extraction, an MS2 bacteriophage was added to each sample as an internal extraction control [28].

II.VI. Pathogen screening
RNA/DNA of all obtained mosquito and serum samples were tested for the presence of RVFV-specific RNA as well as for RNA from flaviviruses and orthobunyaviruses.
II.VI.I. Rift Valley fever phlebovirus detection. A quantitative real-time PCR (qRT-PCR) [29] using the QuantiTect Probe RT-PCR Kit (Qiagen, Hilden, Germany) was performed to verify the presence of RVFV-specific RNA. To quantify the present viral RNA, a synthetic RNA calibrator was used [30]. Samples that contained more than one copy/μl (5 copies/reaction) of RVFV-specific RNA were considered as positive [29].

II.VII. Blood meal analysis
Extracted RNA/DNA from blood-fed mosquitoes was additionally used for blood meal analysis to infer host preferences of mosquito species and thus to determine possible reservoir hosts of RVFV.
A PCR specific for mitochondrial cytochrome b of game species [32] was performed using the QuantiTect Multiplex PCR NoROX Kit (QIAGEN, Hilden, Germany). PCR products were verified by gel electrophoresis in a 1.5% agarose gel. A 100 bp DNA ladder (peqGOLD, VWR International (Part of Avantor), Pennsylvania, USA) was used to identify specific PCR products (464 bp).
Additionally, a PCR specific for mitochondrial 16S ribosomal RNA of vertebrates was carried out using previously published primers [33]. The PCR protocol was modified from Schlegel et al. [34]. A reaction volume of 25 μl containing 3 μl of template DNA, 10 pmol of each primer, 25 mM MgCl 2 , 10 mM dNTP Mix, 5× GoTaq buffer and 5 U GoTaq G2 Flexi DNA Polymerase (Promega Corporation, Fitchburg, WI, USA) was used. Verification of PCR products was performed by gel electrophoresis in a 1.5% agarose gel. To identify specific PCR products (244 bp), a 200 bp DNA ladder (Jena Bioscience GmbH, Jena, Germany) was used.
Gels were stained with ethidium bromide for evaluation. PCR products of samples showing a specific band in the gel were sent for sequencing and analyzed as described before (II.VI.II.).

II.VIII. IgM Capture ELISA
Heat-inactivated cattle sera were tested for the presence of IgM antibodies against RVFV NP with the ID Screen Rift Valley Fever IgM Capture ELISA for ruminants (IDvet, Grabels, France). The ELISA was conducted according to the manufacturer's instructions.

II.IX. Virus isolation
For qRT-PCR-positive mosquito samples, propagation of the virus on cells was attempted. To prevent secondary cell infection, penicillin, streptomycin, amphotericin and gentamicin were added to culture medium (MEM).
II.IX.I. Mosquitoes. 100 μl of the supernatants (II.V.) of mosquito samples that had tested positive in qRT-PCR were diluted in 900 μl MEM and subsequently filtered (Millex-GP, 0.22 μm; Merck KGaA, Darmstadt, Germany). 400 μl each of the filtered samples were added to a well of a 6-well plate with 90% confluent monolayers of Vero 76 cells (African green monkey kidney cells, Collection of Cell Lines in Veterinary Medicine, Friedrich-Loeffler-Institut, Germany) and to a well of a 6-well plate with 90% confluent monolayers of C6/36 cells (Aedes albopictus larval cells, Collection of Cell Lines in Veterinary Medicine, Friedrich-Loeffler-Institut, Germany). Cells were incubated at 37˚C (Vero 76) or 28˚C (C6/36) and 5% CO 2 respectively, and checked daily for the presence of a cytopathogenic effect (CPE). Cell culture supernatants were harvested and tested in each of the two qRT-PCRs after a seven-day incubation or until CPE was detected. 400 μl of these cell culture supernatants were again passaged on 90% confluent monolayers of both Vero 76 and C6/36 cells. After incubation for one week, cell culture supernatants were tested in qRT-PCR for the presence of viral RNA (as described before). II.IX.II. Serum samples. 50 μl of the serum samples that showed evidence of IgM antibodies against RVFV were diluted in 150 μl MEM and added each to a well of a 12-well plate with 90% confluent monolayers of Vero 76 cells. Cells were kept at 37˚C, 5% CO 2 and checked daily for the presence of CPE. After a maximum of seven days, cell culture supernatants were harvested and tested in the qRT-PCR for the presence of RVFV-specific RNA.

II.X. Indirect RVFV immunofluorescence assay (IIFA)
Vero 76 cells that have been exposed to RVFV qRT-PCR-positive mosquito supernatants or IgM-positive sera for one week (II.IX.) were fixed with 4% paraformaldehyde. Subsequently, an IIFA to verify RVFV infection of these cells was performed as previously described [35]. A monoclonal antibody against RVFV NP was used as first antibody. Fixed cells infected with RVFV 35/74 strain (accession number: JF784386-88) served as positive control.

II.XI. High-throughput sequencing
qRT-PCR-positive samples were used for high-throughput sequencing (HTS) to obtain more sequence information. A combination of enrichment of viral nucleic acids with RNA baits and following HTS was applied. For this purpose, RNA extracts were subjected to library preparation as detailed described [36]. Virus nucleic acids were subsequently enriched using myBaits (Arbor Biosciences, Ann Arbor, MI, USA) with the VirBaits panel according to Wylezich et al. [37] with a hybridization time of 24 hours at 65˚C. The bait panel includes 539 baits specific for RVFV. An extended panel (VirBaits 2.0) was used for the dengue virus containing samples that includes 2804 baits specific for dengue virus. The Genome Sequencer software suite (versions 2.6; Roche) was applied to execute reference mapping analyses. Genome sequences of RVFV (KX944814, KX944837, KX944860) and DENV (MT261970, MT981085) were used as reference. Obtained contigs were analyzed with BLAST search (https://blast.ncbi.nlm.nih.gov/Blast.cgi) to characterize virus sequences.

II.XII. Phylogenetic analysis
CLUSTAL W was used to align the sequences as implemented in MEGA v.11 software [38]. The best fitting nucleotide substitution model was identified as GTR. Maximum Likelihood (ML) trees were reconstructed using MEGA v.11 software with bootstrap support of 1000 replicates. Finalized trees were visualized using in the FigTree v.1.4.3 program [39].

III.I.I. Collection and species identification.
A total of 4,950 mosquitoes of four genera and 14 species were collected and identified in this study ( Table 1). These included 571 male and 4,379 female mosquitoes, with 258 of the latter having taken a blood meal. Unengorged mosquitoes were grouped into 521 pools, of which 456 pools contained females and 65 pools contained males. Since engorged mosquitoes were analyzed individually, a total of 779 mosquito samples were examined. Comparing the sampling regions, 59.6% of specimens were collected in Nouakchott and its surroundings, while 36.9% were collected in Trarza and 3.5% in Hodh El Gharbi. Looking at the sampling over the year, most mosquitoes were captured in July and December (S1 Fig).
The majority of mosquitoes belonged to the genus Culex spp. (4,138 individuals), followed by the genera Anopheles spp. (599 individuals) and Mansonia spp. (149 individuals). Fewest mosquitoes were collected within the genus Aedes spp. (64 individuals). The most frequently occurring mosquito species was Culex quinquefasciatus (38%), followed by Culex poicilipes (15%) and Culex tritaeniorhynchus (12%). Within the other genera, Anopheles pharoensis (11%) represented the most abundant species (Table 1). Comparing the sampling regions, Cx. quinquefasciatus represented the most common species in Nouakchott ( Table 2) and Hodh El Gharbi (Table 3), while in Trarza the majority of mosquitoes consisted of Cx. poicilipes and An. pharoensis ( Table 4). Collection at most sampling sites was performed only once during the study. However, in Nouakchott two locations (Socogim Le Ksar and the Botanical Garden in Sebkha) were sampled twice on different dates ( Table 2). For both locations, the most frequently collected species remained the same at both times (Cx. quinquefasciatus), but the abundance of other species changed depending on the date of sampling.
III.I.II. RVFV detection. RVFV-specific RNA was found (1,783 copies/μl of viral RNA; Ct-value of 28) in one of the 779 mosquito samples tested. The sample contained a mosquito pool of ten female Anopheles pharoensis mosquitoes collected in December 2018 on the farm in Rosso (Fig 1 and Table 4), where clinical RVF cases were observed in cattle.
The HTS results are shown in Table 5. Sequence alignments were generated for the eight contigs using all the available RVFV sequence data in GenBank (NCBI, Bethesda, USA). The contigs covered all three segments (S, M, L) and revealed a close relation to RVFV-isolates from South Africa, Mauritania and Namibia (accession numbers: OK392020, OK415590, OK415591, OK415592, OK415593, OK415594, OK415595, OK415596). In the attempt of virus isolation, no CPE was observed in either cell line during the first and second cell passage. RVFV qRT-PCR revealed the presence of 7.54 copies/μl viral RNA on Vero 76 cells and 3.22 copies/μl viral RNA on C6/36 cells in cell culture supernatants of the first cell passage after seven days incubation. However, cell culture supernatants of the second cell passage showed no evidence of RVFV-specific RNA. Likewise, in IIFA no evidence of replicable RVFV was observed in these cells, indicating that viral RNA detected in supernatants of the first cell passage was derived from the original sample.
III.I.III. Flavivirus and Orthobunyavirus detection. In qRT-PCR, two out of 779 mosquito samples showed melting curves similar to that of Usutu virus (positive control), thus indicative for flaviviruses. Sequencing of qRT-PCR-products of these samples revealed the presence of dengue virus (DENV, family Flaviviridae, genus Flavivirus) RNA in both mosquito pools. The first sample consisted of a pool of eight female Aedes aegypti mosquitoes that were captured in the town of Rosso (Fig 1) in December 2018. The second sample contained a pool of ten female Culex quinquefasciatus mosquitoes that were captured at the same collection site ( Table 4).
Using HTS, partial genome sequences of both samples could be generated. For the positive Aedes pool a sequence of 572 bp (accession number: OK384856) was detected (530 reads). A sequence of 5076 bp (5965 reads) could be generated for the positive Culex sample (accession number: OK384579). The alignment of these sequences revealed highest identity with other DENV strains isolated in 2018 from human sera in West Africa. The Aedes aegypti-derived DENV sequence had 99.8% sequence homology with an October 2018 isolate from Mauritania (MT981085.1) and the Culex quinquefasciatus-derived sequence had 99.9% sequence Anopheles  (Fig 2).
In the attempt of virus isolation of these two samples that showed evidence of dengue virusderived RNA, neither CPE nor dengue virus RNA was detected in either cell passage.
For orthobunyaviruses, no evidence of viral RNA was found in the mosquito samples. III.I.IV. Blood meal analysis. The source of blood meals was identified for a total of 196 out of the 258 blood-fed mosquitoes. The cytochrome b and 16S ribosomal RNA banding patterns and sequences yielded identical results for 160 blood meal samples. For 22 blood meal samples, only specific cytochrome b banding patterns and sequences were found, while for 14 other blood meal samples, only specific 16S ribosomal RNA banding patterns and sequences were detected (S1 Table). Engorged mosquitoes of which the identification of blood meal was successful were among eleven of the captured species ( Table 6). Over 50% of the mosquitoes fed on humans (Homo sapiens), followed by almost 35% of the mosquitoes that fed on cattle (Bos taurus/indicus) (Fig 3). For about 15% of the mosquitoes, other feeding hosts were detected, including small ruminants (Capra hircus, Ovis aries), donkeys (Equus asinus), cats (Felis spp.) and dogs (Canis lupus; dog-like carnivores) as well as straw-colored fruit bats (Eidolon helvum) ( Table 6). Most mosquitoes collected in urban areas fed on humans whereas those captured in rural areas mostly fed on cattle (captured next to a cattle farm) and donkeys (near rice fields) (Fig 3).

III.II.I. RVFV detection.
In December, when RVF disease (abortions, fever, hypersalivation) was observed on the farm in Rosso, six out of 16 (37.5%) Montbéliarde cattle had detectable IgM antibodies against RVFV. In sera of local cattle sampled one month earlier on the same farm, IgM antibodies against RVFV were detected in three out of 28 (10.7%) animals (Fig 4). No evidence of RVFV-derived RNA was detected in any of the 44 tested sera and the examination of IgM positive sera revealed no evidence of replicable RVFV.

III.II.II. Flavivirus and Orthobunyavirus detection.
No evidence of Flavivirus-specific or Orthobunyavirus-specific RNA was found in any of the 44 serum samples.

IV. Discussion
One of the aims of this study was to elucidate the abundance of RVFV-transmitting mosquitoes and the presence of the virus in vectors in Mauritania. As amplification hosts that promote RVFV maintenance during the enzootic cycle remain unidentified to date [5], blood meals of mosquitoes were analyzed to obtain information on mosquito host preferences. Furthermore, the study aimed to examine the occurrence of flavi-and orthobunyaviruses in mosquitoes in Mauritania. To achieve these objectives, 4,950 mosquitoes were collected during 2018 in three southern regions of Mauritania (Fig 1) where RVF outbreaks have previously occurred [9,40]. Fourteen different mosquito species were identified, comprising four genera that have already been https://doi.org/10.1371/journal.pntd.0010203.g002 Table 6. Blood meal sources (hosts) of blood-fed mosquitoes.  Table 1) [12]. Consistent with previous studies, Culex spp. constituted the most abundant mosquito genus [13,41]. As species abundance of mosquitoes in Mauritania varies depending on the season [15] and most locations were only sampled once during the year, limited conclusions can be drawn about the seasonal species distribution in  the regions. Furthermore, it is possible that diurnally active species, such as many Aedes spp., may have been underrepresented due to the collection method used. Eleven of the captured mosquito species have previously been described as RVFV carriers ( Table 1) [8]. In this study, we found evidence of RVFV in a pool of female Anopheles pharoensis mosquitoes ( Table 4). RVFV infection of this species has previously been detected in Kenya [7,8], but to our knowledge this is the first description of RVFV in An. pharoensis in Western Africa. This finding emphasizes the need of performing vector competence studies, as only these can clarify whether the mosquito species is capable of transmitting RVFV from one host to another. Comparison of the RVFV contigs using the BLAST tool (NCBI, Bethesda, USA) revealed a close relationship to isolates from South Africa, Namibia, and Mauritania ( Table 5), but it is difficult to draw conclusions about a geographic phylogeny from these results due to the overall highly conserved nature of the RVFV genome [42]. The RVFV-positive mosquitoes were collected on a farm in Rosso (Fig 1) while cattle on the farm exhibited symptoms of RVF disease. The recency of the RVF epizootic was confirmed by the detection of RVFV-specific IgM antibodies in bovine sera collected on the farm, as IgM antibodies in cattle persist only during the first few months after RVFV infection [2]. However, it can be assumed that the epizootic had already started prior to the observed clinical manifestation, since IgM antibodies were also detected in sera taken a month earlier and no evidence of the virus itself was found in any of the blood samples. Viremia in infected cattle lasts only for about seven days [43] and had probably already subsided in the sampled animals.

Genus Species Homo sapiens Bos taurus / indicus Capra hircus Ovis aries Equus asinus Canis lupus � Felis spp. Eidolon helvum Total
In order to investigate RVFV maintenance, the majority of mosquitoes (4,241 individuals) in this study were collected during the absence of reported RVF cases. Other studies have previously revealed the presence of the virus in mosquitoes during the enzootic cycle [44,45], but these data remain limited because virus detection during these periods is difficult due to low mosquito infection rates [46,47] and sparse transmission to susceptible hosts [16]. However, evidence of active RVFV circulation was found only in those mosquitoes that were additionally captured (709 individuals) in close proximity to animals with confirmed RVF disease. In addition, transovarial RVFV transmission within Aedes spp. mosquitoes is believed to be a key factor in RVFV maintenance [1,48]. Yet there is little data available to support this type of maintenance [49], and it has never been confirmed in Western Africa [1]. To verify its occurrence within different mosquito genera in Mauritania, in addition to female mosquitoes, captured males were also examined, which do not feed on vertebrates but exclusively on plants. However, none of the 571 tested male mosquitoes caught in the absence of RVF cases showed evidence of RVFV infection. Future collection and analyses of male mosquitoes, as well as of larval and egg stages of mosquitoes during epidemics will help to clarify the role of vertical RVFV transmission in Mauritania.
Wildlife capable of acting as amplification hosts may be another factor favoring RVFV maintenance [1]. To identify mosquito hosts and thus animals possibly involved in the RVFV transmission cycle, blood meals of 258 engorged mosquitoes were examined. Similar to other studies in Mauritania, where mosquitoes of the genus Anopheles spp. were analyzed, the vast majority of mosquitoes fed on humans (urban areas) and cattle (rural areas) (Fig 3) [50,51], depending on the availability of these feeding hosts. This reflects the potential risk posed by infected mosquitoes, as both humans and cattle are known to be highly susceptible to RVFV [4]. A small proportion of the engorged mosquitoes used other hosts to feed. In line with previous investigations, mosquitoes also fed on small ruminants (goats, sheep), donkeys and dogs (dog-like carnivores) [51,52], and this study additionally identified cats and straw-colored fruit bats (Eidolon helvum) as sources of blood meals ( Table 6). The identification of fruit bat blood in the mosquitoes is of particular interest as bats have been repeatedly suggested as RVFV reservoir [5,53,54]. The host-vector interaction between Eidolon helvum and mosquitoes has also been reported in other regions with endemic RVFV circulation [55]. Moreover, RVFV and specific antibodies have been detected in several bat species in Africa [53,56,57,58], and experimental infection studies have demonstrated a variety of bat species to be susceptible to the virus [5,53,59]. However, the definite role of bats in RVFV ecology remains undetermined [5] and should be investigated more closely. Interestingly, no birds were found as feeding hosts in this study, which is in contrast to studies in North America that found birds to be the primary hosts of Culex mosquitoes [60].
Furthermore, evidence of DENV circulation was found in two mosquito pools collected in December in the town of Rosso (Fig 1 and Table 4). To our knowledge, this is the first description of DENV detected in mosquitoes in Mauritania. Dengue fever is caused by four DENV serotypes (DENV 1-4). An additional serotype (DENV-5) has been described, but it is currently limited to a single outbreak in Asia [61]. The DENV strains detected in this study showed highest identity with DENV-2 strains isolated in West Africa (Fig 2). This is not surprising given the results of other studies that have described DENV-2 as the dominant serotype in Africa [62]. The closest genetic proximity was found to two sequences isolated from human sera in Mauritania and in Senegal, also in 2018. As the DENV-positive mosquitoes in this study were collected in Rosso, which is close to the Senegalese border, these results, alongside with the previously detected sequences in patients, prove the epidemic circulation of DENV-2 in this geographic region. The first evidence of DENV-2 was found in a mosquito pool containing female Aedes aegypti mosquitoes, primary vectors of the virus [23]. The second DENV-2-positive pool consisted of female Culex quinquefasciatus mosquitoes known as vectors for West Nile virus, another virus of the genus Flavivirus [63,64]. Early on, this species has been discussed as potential vector for DENV, but published data are very contradictory [23]. However, the virus has been previously isolated from other Culex spp. mosquitoes [65], indicating the need for further studies to evaluate the role of these mosquitoes in DENV transmission.
To conclude, evidence of RVFV as wells as DENV was found in mosquitoes collected in Mauritania in 2018. Furthermore, it was demonstrated that mosquitoes feed on fruit bats, which are suspected to be involved in RVFV maintenance. In order to gain a thorough understanding of RVFV ecology, further in-depth studies are required to investigate factors promoting RVFV maintenance. As discussed by Bhatt et al., the burden caused by DENV in Africa may be largely underestimated [20]. Its occurrence in Mauritania needs to be investigated further, since very little is known to date. Although no other mosquito-borne viruses were detected in this study, several other arboviruses are circulating in Mauritania, threatening human and animal health [15,17,18]. This again underlines the need for research on the occurrence of arboviruses and their vectors in order to be able to promote their control and prevention.