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Original Article 

The Prevalence of Antibodies against Sandfly Fever Viruses and West Nile 

Virus in Cyprus 
 

Gaetan Billioud; Christina Tryfonos; *Jan Richter 
 

Department of Molecular Virology, Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus 

 
(Received 14 Oct 2017; accepted 2 Jan 2019) 

 

Abstract 
Background: Sandfly fever is an incapacitating disease caused by sandfly-borne Phleboviruses that can lead to men-

ingitis, encephalitis or meningoencephalitis. West Nile virus (WNV), a mosquito-borne Flavivirus, can induce neu-

roinvasive disease manifested by meningitis, encephalitis or acute flaccid paralysis. Both vectors are endemic in Cy-

prus and very active during summer. The aims of this study were to determine first the prevalence of sandfly fever 

viruses (SFV) and WNV infections in Cyprus and second, to investigate their role in central nervous system (CNS) 

infections. 

Methods: For the prevalence study, 327 sera collected in 2013 and 2014 were tested for anti-SFV and anti-WNV 

IgG using indirect immunofluorescence assay and ELISA, respectively. In order to investigate a possible role of SFV 

and WNV in CNS infections, 127 sera of patients presenting symptoms of SFV or WNV infections were screened for 

IgM specific to SFV and WNV. 

Results: The overall anti-SFV IgG seroprevalence was 28% and was increasing with age (P< 0.01). The seropreva-

lence rate for anti-WNV IgG in Cyprus was 5%. Concerning the role of SFVs in CNS infections, anti-SFV IgM was 

detected in 8 out of 127 sera from selected patients presenting relevant symptoms of infections during vector’s active 

period. In addition, anti-WNV IgM were detected in 17 out of the 127 patients with compatible symptoms. 

Conclusion: The findings confirm the presence of sandfly fever and WNV in Cyprus and should, therefore, be con-

sidered in the differential diagnosis of patients with febrile illness/meningitis. 

 
Keywords: Phleboviruses; West-Nile virus; Cyprus; Seroprevalence 

 
Introduction 
 

Sandfly (Diptera: Psychodidae)-transmit-

ted phleboviruses may cause a transient and 

moderate febrile illness (named pappatasi fe-

ver, 3-day fever or sandfly fever) but can al-

so affect the central nervous system (CNS) 

leading to serious infections. The most com-

mon vectors are Phlebotomus papatasi, P. 

perfiliewi or P. perniciosus. The genus Phlebo-

virus has been recently assigned to the newly 

created family Phenuiviridae and the order 

Bunyavirales (1).  

Sandfly-borne phleboviruses are enveloped 

negative-sense and single-stranded tripartite 

RNA viruses classified around two viral species 

(Sandfly fever Naples (SFNV) and Salehabad) 

and two tentative species (Sicilian and Corfu).  

 

 
Infections with SFNV and Sandfly fever 

Sicilian (SFSV) viruses are clinically similar 

and characterized by high fever, headache, ret-

ro-orbital pain, malaise, diarrhoea, myalgia, 

photophobia and anorexia along with throm-

bocytopenia, leukopenia and elevated liver en-

zymes (2, 3). Toscana virus, a member of the 

Naples serogroup, generally induces a mild 

febrile illness without CNS involvement.  

However, when the CNS is affected, high 

fever, headache, nausea, vomiting, Kernig 

signs, neck rigidity, myalgia and sometimes 

unconsciousness, tremors, paresis and nys-

tagmus as well as encephalitis, severe me-

ningoencephalitis and long-lasting sequelae 

have been reported (4, 5). The Mediterranean 

*Corresponding author: Dr Jan Richter, E-mail: 
richter@cing.ac.cy 



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basin is endemic for sandfly-borne phlebovirus-

es infections (4, 6-10) and particularly Cy-

prus where phlebotomines (11, 12) and out-

breaks have been reported (13-16). 

Regarding West Nile fever, the majority 

of clinical cases are mild and present with 

flu-like symptoms characterized by fever, ma-

laise, and myalgia frequently accompanied by 

rash. Severe cases with signs of encephalitis, 

meningoencephalitis or meningitis are rare 

(<1%), most often observed among elderly 

and associated with a 10% fatality rate (17). 

The disease results from an infection by West 

Nile Virus (WNV) (genus Flavivirus, family 

Flaviviridae, order unassigned) transmitted 

through a mosquito (Diptera: Culicidae) bite, 

mostly from the genus Culex and usually from 

the Culex pipiens complex (18), abundant in 

Cyprus (19, 20). Human infection is solely 

incidental of the enzootic transmission cycle 

between avian natural hosts and mosquito vec-

tors (21). The virus is considered to be one of 

the most important emerging arboviruses in re-

cent years because of the multiple outbreaks 

reported in Europe and particularly in the Med-

iterranean area (Greece, Turkey, Spain) (22, 

23). To date, no epidemiological data for WNV 

have been reported for Cyprus but the first neu-

roinvasive case was reported in 2016 (24, 25) 

and a second confirmed case in 2018 (ECDC 

update), confirming the presence of the WNV 

in the island. 

Because of outdated or absent epidemio-

logical data concerning Cyprus, a cross-sec-

tional serologic survey was conducted to es-

timate SFV and WNV IgG respective sero-

prevalences in order to assess the exposure 

of the Cypriot population to these pathogens. 

In addition, the possible role of these patho-

gens in CNS infections in Cyprus was inves-

tigated by testing for markers of recent infec-

tion (IgM) and viral RNA in samples of pa-

tients with febrile illness and/or CNS infec-

tion. 

 

Materials and Methods 
 

Sample collection 

Serum and cerebrospinal fluid (CSF) sam-

ples from patients were received at the Cyprus 

Institute of Neurology and Genetics, stored ap-

propriately at -20 °C and used subsequently. 

For IgG seroprevalence, 327 samples between 

Jan 2013 and Dec 2014 were retrospectively 

selected following a leftover sampling method-

ology matching the 2013 census Cypriot de-

mography according to patient’s sexes (male 

or female), age and origin of the sample (Fa-

magusta, Larnaca, Limassol, Nicosia or Pa-

phos district) (Fig. 1). Informed consent was 

taken from the patients before participation. 

The patients with known disease, medical 

procedure or treatments affected the antibod-

ies detection were excluded (i.e. autoimmune 

disease, immunomodulatory treatments, trans-

planted, neoplasm, etc.). Determination of spe-

cific IgM was performed on samples received 

during 2013 and 2014 vector active season 

(warm months, from May to Nov in Cyprus) 

from 127 selected patients with infectious path-

ologic features relating to Sandfly or West 

Nile fevers. Based on similar selection crite-

ria, 72 CSF samples from patients collected 

between 2015 and 2016 during vector active 

season were tested for circulating viral RNA. 

 

SFV IgG and IgM detection 

Overall, 327 and 127 sera were analyzed 

for the presence of anti-SFV IgG and IgM, re-

spectively, by indirect immunofluorescence test 

(IIFT) BIOCHIP Mosaic™: Sandfly Fever Vi-

rus IgG or IgM (EUROIMMUN, Lübeck, Ger-

many). This test is the only commercially avail-

able test that offers the possibility to assess the 

presence of antibody reacting against two spe-

cies members of the Sandfly Sicilian serogroup 

(SFSV and Sandfly fever Cyprus viruses, 

SFCV) and two members of the Sandfly Naples 

serogroup (SFNV and Toscana virus, TOSV), 



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without excluding the possibilities of cross-

reactivity. 

Sera were diluted 100 and 50 times in sam-

ple buffer for IgG and IgM, respectively, and 

tested according to the manufacturer’s instruc-

tions. Before determining specific anti-SFV 

IgM, IgG antibodies and rheumatoid factors 

of class M were removed by immune-absorp-

tion using the Siemens RF-Absorbent (Mar-

burg, Germany) [Ref: OUCG194] for 15min at 

room temperature. Samples were considered 

positive if in some cells, but not all, cytoplas-

mic finely granular structures and inclusion bod-

ies fluoresced with the same pattern obtained as 

for the positive control serum. 

 

WNV IgG and IgM detection 

Overall, 327 sera were collected for spe-

cific anti-WNV IgG detection and 127 sera for 

IgM detection, respectively, using an FDA-ap-

proved enzyme-linked immunosorbent assay 

(ELISA) (EUROIMMUN, Lübeck, Germany). 

Sera were diluted 100 times for both IgG and 

IgM in sample buffer (containing IgG/RF-Ab-

sorbent for IgM detection) and tested accord-

ing to the manufacturer’s instructions. The sam-

ples were considered positive when the ratio be-

tween the extinction values of the samples over 

the calibrator (20 RU/ml for IgG) was ≥ 1.1. 

 

Viral RNA extraction and RT–PCR ampli-

fication 

Viral RNA was extracted from 72 CSF 

samples using 400μl of clinical specimen by 

the iPrep™ PureLink® Virus kit according to 

manufacturer’s instructions and resuspended 

in 100μl DEPC water. Ten microliters of the 

extracted viral RNA was used as a template 

using specific primers with the SuperScript® 

III Platinium One-Step qRT-PCR kit (Invitro-

gen, USA), according to the manufacturer’s 

instructions. For Phlebovirus detection and 

quantification, the specific primers used am-

plified the 3’ end of the small segment N gene 

and were based on published protocols (26, 27). 

For Flavivirus detection and quantification, the 

specific primers targeted the NS5 gene and were 

based on a previously published protocol (28). 

 

Statistics 

Results were statistically analyzed with the 

Prism™ version 5.01 software from GraphPad 

(La Jolla, CA, USA). Along with descriptive 

statistics, univariate analysis was conducted on 

the results obtained from the seroprevalence 

study by Fisher’s exact tests. Comparison of 

groups’ average age was analyzed by nonpar-

ametric two-tailed Mann-Whitney tests. The lo-

gistic regression model was generated from the 

GNU package R environment. P< 0.05 indi-

cated statistical significance. 

 

Results 

 

Prevalence study of anti-sandfly fever viruses 

and West Nile virus IgG antibodies 

To determine the exposure of Cypriots to 

sandfly fever viruses, 327 human serum sam-

ples from 2013–2014 were screened for anti-

SFVs and anti-WNV IgG. The sampling was 

distributed by sex and age proportional to Cy-

prus’ population (Table 1). By sex, 166 were fe-

males (~51%) and 161 males (~49%). By age 

groups, 81 were <20yr old (~25%), 184 aged 

20–60yr (~56%), and 62 were aged >60yr 

(~19%) with an overall mean age of 37yr old. 

By districts, 9 specimens were from Famagu-

sta (~3%), 32 from Larnaca (~10%), 107 from 

Limassol (~33%), 170 from Nicosia (~52%) 

and 9 were from Paphos District (~3%) (Fig. 

1). 

The overall seroprevalence of anti-SFVs 

IgG was 28% (CI95%: 23.5–33.4%) and in-

creased with age (Table 1). Difference of mean 

age in anti-SFV seropositive group (47yr old) 

compared to the seronegative patient's group 

(33yr old) was statistically significant (P< 

0.0001). Logistic regression model confirmed 

the trend (P< 0.001) and computed an increased 

risk of ~3% per year (SE 0.6%). Differences 

observed in seroprevalence for anti-SFV IgG 

between females (~25%) and males (~31%) 



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or between districts (Famagusta: ~0%, Larnaca: 

~19%, Limassol: ~31%, Nicosia: ~30% and 

Paphos: ~33%) were not statistically significant 

(P> 0.05) (Table 1). Difference in prevalence 

between sera reacting only against SFSV and/or 

SFCV (~12%) and sera reacting only against 

SFNV and/or TOSV (~11%) was not statisti-

cally significant (P> 0.05) (data not shown). 

The same 327 human sera from 2013–2014 

were also screened for anti-WNVs IgG. The 

overall seroprevalence of anti-WNV IgG was 

~5% (CI95%: 2.5–7.2%) (Table 1). The dif-

ference of mean age in anti-WNV seropositive 

group (33yr old) compared to the seronegative 

patients group (37yr old) was not statistically 

significant. Differences in frequencies observed 

between each age group, sex and district were 

also not statistically significant. 

Five patients (~1.5%) were found to have 

IgG antibodies reacting against both SFVs and 

WNV (data not shown), giving seroprevalence 

rates of ~31% (5/16) and ~5% (5/93) of anti-

SFVs and anti-WNV IgG in anti-WNV and 

anti-SFVs IgG positive groups, respectively. 

The differences of rates in positive groups 

compared to the general population (~28% and 

~5% for anti-SFV and anti-WNV IgG, respec-

tively) were not statistically significant. 

 

Role of SFV and WNV infections in CNS 

infections in Cyprus 

To assess the morbidity of SFV infections 

in Cyprus, human sera from patients display-

ing infectious pathologic features in 2013 and 

2014 during sandflies’ active period were test-

ed for markers of recent SFV infection, IgM. 

Eight sera (~6%) were found positive for anti-

SFV IgM out of the 127 selected patients (Ta-

ble 2). Difference of SFV IgM seroprevalence 

rates between each age group, sex and district 

were not statistically significant. However, a 

higher frequency of samples reacting only 

against SFV serotypes belonging to the Naples 

serogroup (SFNV and TOSV, 7/127) than to 

the Sicilian serogroup (SFSV and SFCV, 0/ 

127) (data not shown) was statistically sig-

nificant (P< 0.05). Three of the 8 anti-SFV IgM 

positive patients (~38%) showed neuroinvasive 

features (meningitis or meningoencephalitis) 

but no statistical significance was found com-

pared to the anti-SFV IgM negative group (34/ 

127, ~26%, P> 0.05) (data not shown). Of the 

8 seropositive patients for anti-SFV IgM, four 

patient’s CSF were available and three of them 

were also found positive for anti-SFV IgM (da-

ta not shown). All CSF positive for SFV IgM 

reacted only against the Naples serocomplex, 

further confirming their neuroinvasion capa-

bilities. 

Detection of Phlebovirus nucleic acids by 

specific quantitative RT-PCR in 72 human cer-

ebrospinal fluid samples from patients display-

ing infectious pathologic features in 2015 and 

2016 during sandflies’ active period was per-

formed, but no specimen was found positive 

(data not shown). 

Seventeen (~13%) out of the 127 tested hu-

man sera from patients displaying infectious 

pathologic features in 2013 and 2014 during 

mosquito’s active period were found positive 

for anti-WNV IgM (Table 2). The difference 

of WNV IgM seroprevalence rates between 

sexes, age groups or districts were not found 

statistically significant. Two of the 17 anti-

WNV IgM positive patients (~12%) showed 

neuroinvasive features (meningitis or menin-

goencephalitis) but no statistical significance 

was found compared to the anti-WNV IgM neg-

ative group (29/110, ~26%) (data not shown). 

With regard to nucleic acid testing, no 

WNV RNA was detected in the 72 human CSF 

samples from selected patients displaying in-

fectious pathologic features in 2015 and 2016 

during mosquitos’ active period (data not 

shown). 

 

 

 

 

 

 



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Table 1. Sandfly fever virus and West Nile IgG seropositivity 
 

  SFV IgG WNV IgG 

  Tested Positive % Positive % 

Total 327 93 ~28 16 ~5 

Males 161 52 ~32 6 ~4 

Females 166 41 ~25 10 ~6 

< 20 y 81 6 (*) ~7 4 ~5 

20–60 y 184 60 (*) ~33 11 ~6 

> 60c y 62 27 (*) ~44 1 ~2 

Famagusta 9 0 0 0 0 

Larnaca 32 6 ~19 1 ~3 

Limassol 107 33 ~31 5 ~5 

Nicosia 170 51 ~30 10 ~6 

Paphos 9 3 ~33 0 0 

 

SFV, sandfly fever viruses; WNV; (*), Statistically significant (P< 0.05) 

 
Table 2. Sandfly fever virus and West Nile IgM seropositivity 

 

  SFV IgM WNV IgM 

  Tested Positive % Positive % 

Total 127 8 ~6 17 ~13 

Males 58 6 ~10 5 ~9 

Females 69 2 ~3 12 ~17 

< 20 y 52 2 ~4 8 ~15 

20–60 y 54 4 ~7 7 ~13 

> 60c y 21 2 ~10 2 ~10 

Famagusta 5 0 0 2 ~40 

Larnaca 10 0 0 0 0 

Limassol 41 6 ~15 9 ~22 

Nicosia 66 2 ~3 6 ~9 

Paphos 5 0 0 0 0 

 

SFV, sandfly fever viruses; WNV 

 

 
 

Fig. 1. Illustrative map of Cyprus’ districts. White, Area studied; Grey, Non-government controlled area; Dark grey, 
UN buffer zone; Light grey, UK sovereign bases 



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Discussion 
 

Because the presence of arboviruses in Cy-

prus had been reported previously (15, 24, 29-

32), we evaluated the residents’ exposure to 

SFV and WNV following Cyprus’ demography 

in terms of age, sex and location. 

The overall seroprevalence rate for anti-

SFVs IgG estimated in this study was ~28%. 

Higher seroprevalence of antibodies against 

SFSV virus (~62%) and neutralizing antibodies 

against SFNV (~57%), SFSV (~32%) and 

TOSV (~20%) viruses were reported in pre-

vious studies on Cypriot residents (33, 34). A 

recent seroprevalence study of phleboviruses 

in Cypriot dogs indicated also high neutraliz-

ing rates for SFSV (~60%) and TOSV (8.4%) 

(35). Lower rates found here may reflect the 

different specificity and sensitivity of the as-

say used (IIFT or plaque neutralization reduc-

tion assay (PRNT) (36), sampling method 

skewed towards specific geographical areas 

(Famagusta, Larnaca or Paphos districts), test 

subjects (healthy donors or symptomatic pa-

tients), species tested (humans or dogs) or simp-

ly a lower exposition of the modern Cypriot 

population, possibly due to arthropods abate-

ment programs to eradicate malaria in the is-

land (37). 

Direct comparison with studies depicting 

SFV seroprevalences from neighbouring coun-

tries is limited, mostly because of the wide use 

of PRNT and the focus on TOSV. However, 

our study reports comparable anti-SFV IgG 

seroprevalence rates described in Turkish Cen-

tral/Northern Anatolia (~33%) (38) but lower 

compared to the Turkish Mersin Province 

(~67%) (39), both tested by IIF. 

The anti-SFV IgG seroprevalence rate in-

creasing with age is in agreement with the con-

clusions of previous studies (40, 41) and demon-

strates that the Cypriot population is exposed 

to SFVs throughout life. Unfortunately, other 

risk factors previously identified such as living 

in rural areas or high levels of outdoor activity 

could not be assessed because of the lack of  

 

 

patient’s information. 

Concerning WNV, the overall IgG sero-

prevalence found in Cyprus was 5% and the 

difference of rates between sexes, age groups 

or districts were not statistically significant. It 

is the first time that anti-WNV IgG seropreva-

lence has been estimated in Cyprus. WNV-spe-

cific IgG rates were lower in neighbouring 

countries such as Greece (2.1%) (42), Northern 

Italy (0.3–2.1%) (43) or South-Eastern France 
(1.4%) and higher in Libya (13.1%) or Tunisia 

(12.5%) (44) but more similar to Turkey (2.4–
12.1%) (20, 45), Algeria (6.7%) or Serbia (~4%) 

(46). 

In addition, the SFV IgG seropositivity rate 

in the WNV IgG seropositive group (~31%) 

was comparable to the rate found in the entire 

population (29.4%). Similarly, the WNV IgG 

seropositivity proportion in the SFV IgG se-

ropositive group (~5%) was analogous to the 

sample population tested in this study (~5%). 

This supports the hypothesis of random chance 

to contract each viral infection. 

Regarding the role of SFV in CNS infec-

tions in Cyprus, we identified samples (8/ 

127) with markers of recent SFV infection 

(IgM) in patients presenting symptoms akin 

to sandfly fever, supporting a role of SFVs in 

the aetiology of febrile illnesses/meningitis in 

Cyprus. 

Distinction between antigenically related 

viruses amongst the sandfly fever Naples spe-

cies (i.e. SFNV and TOSV) and virus closely 

related to Sandfly fever Sicilian virus (i.e. 

SFSV and SFCV) based on IIFT can be diffi-

cult due to cross-reactivity. However, there was 

a significantly higher rate of sera from symp-

tomatic patients tested for anti-SFV IgM re-

acting only against viruses from the Naples 

serogroup than sera reacting only against vi-

ruses belonging to the Sicilian serogroup. Be-

cause of similar rates observed for IgG be-

tween serogroups and that patients were select-

ed based on relevant symptoms, it confirms that 



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infections from viruses belonging to the Naples 

serogroup are more symptomatic, particularly 

TOSV (47). Anti-SFV IgM specific to mem-

bers of the Naples serogroup are at higher con-

centrations or last longer than the ones specific 

to Sicilian-like viruses (34). However, the de-

tection of anti-SFV IgM specific to the Naples 

serocomplex in the CSF of affected patients 

strongly supports their neuroinvasive pathogen-

esis. 

Possible cross-reactivity with anti-Hanta-

virus and anti-Crimean-Congo hemorrhagic fe-

ver virus (CCHFV) immunoglobulins cannot 

be ruled out based on the IIFT assay used. How-

ever, no hantavirus or CCHFV infection nor 

hemorrhagic fever have ever been reported in 

Cyprus so far. Even though their vectors are 

present on the island (48), it is unlikely that the 

anti-SFV antibodies seroprevalence rates de-

picted in this report are markedly influenced 

due to such cross-reactivity. 

Markers of recent WNV infection (IgM) 

were also detected in patients displaying rel-

evant symptoms, highlighting its circulation and 

morbidity in the Cypriot population. Few se-

ropositive patients had neurological symptoms 

such as meningitis or meningoencephalitis. To-

gether with the first Cypriot symptomatic case 

of a 75yr-old man with confirmed WNV in-

fection during summer 2016 (24), these re-

sults demonstrate the circulation of WNV in 

Cyprus. All the anti-WNV IgM seropositive 

cases were from 2013, following the trend of 

marked decreased West Nile fever autoch-

thonous cases reported in Europe during these 

yr (49). 

Attempts to detect viral genetic material in 

more recent (2015 and 2016) patients’ CSF by 

RT-qPCR following published protocols (26-

28) were unsuccessful. The most likely causes 

for this shortcoming are probably low SFV 

and WNV viremia detectable only in a small 

period of time, usually before patients present 

to the healthcare personnel, the limited number 

of samples tested and the use of direct RT-

qPCR. 

Conclusion 
 

This report provides evidence of signifi-

cant SFV and WNV circulation in Cyprus as 

well as evidence of their pathogenicity among 

Cypriot patients. For these reasons, the surveil-

lance and study of arboviral infections in Cy-

prus should be strengthened as these pathogens 

are potential causes of incapacitating and severe 

neurological diseases. 

 
Acknowledgements 
 

The authors are grateful to Astero Con-

stantinou and Sylvie Pavlides for technical as-

sistance and Dr Christiana Demetriou for sta-

tistical assistance. This study was supported by 

the Cyprus Institute of Neurology and Genetics. 

The authors declare that there is no conflict 

of interests. 

 
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