Literature DB >> 15705333

Mosquitoborne viruses, Czech Republic, 2002.

Zdenek Hubálek1, Petr Zeman, Jirí Halouzka, Zina Juricová, Eva Stovicková, Helena Bálková, Silvie Sikutová, Ivo Rudolf.   

Abstract

Specimens from residents (N = 497) of an area affected by the 2002 flood were examined serologically for mosquitoborne viruses. Antibodies were detected against Tahyna (16%), Sindbis (1%), and Batai (0.2%) viruses, but not West Nile virus. An examination of paired serum samples showed 1 Tahyna bunyavirus (California group) infection.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15705333      PMCID: PMC3294340          DOI: 10.3201/eid1101.040444

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


The 2002 flood in Bohemia struck the Czech Republic just a few years after the 1997 flood (in Moravia and Silesia). Apart from Prague, extensive rural areas along the Vltava and Labe Rivers were flooded in August 2002. In the Mělník area, which offers favorable habitats for mosquitoes under normal conditions (), mass mosquito breeding (largely Ochlerotatus sticticus, Oc. cantans, Aedes vexans, and Ae. cinereus) occurred after August 20. This increased mosquito population peaked September 3–9, with a biting frequency of 70 bites per person per minute. The mosquito population declined during the second half of September and disappeared by November.

The Study

To estimate the risk for infections with mosquitoborne viruses, we screened the human population of the flooded area (Figure 1) for antibodies against the viruses known to occur in central Europe (): Tahyna (TAHV), Orthobunyavirus of the California group, Bunyaviridae; West Nile (WNV), Flavivirus of the Japanese encephalitis group, Flaviviridae; Sindbis (SINV), Alphavirus, Togaviridae); and Batai (BATV), Orthobunyavirus of the Bunyamwera group, Bunyaviridae.
Figure 1

A), Potential foci of mosquitoborne viruses in the Mělník area. Floodplain forests identified on the Landsat MSS satellite images (dotted red line), with hydrology and settlement in background (DMU-200, VTOPÚ Dobruška), and proportion of Tahya virus seropositive residents at particular localities (large, medium, and small circles indicate the risk zones A, B, and C, respectively). B) [inset], radar satellite image of the conflux of the Labe and Vltava Rivers on August 17, 2002 (2 days after the flood culmination), showing extent of floodwater (dark areas). Inundated forests, with subsequent mass occurrences of Ochlerotatus and Aedes mosquitoes, are visible as lighter areas surrounding Labe River upstream of the confluence; scattered lagoons (dark areas) in arable fields along both rivers far left and right turned into breeding sites of predominantly Culex mosquitoes.

A), Potential foci of mosquitoborne viruses in the Mělník area. Floodplain forests identified on the Landsat MSS satellite images (dotted red line), with hydrology and settlement in background (DMU-200, VTOPÚ Dobruška), and proportion of Tahya virus seropositive residents at particular localities (large, medium, and small circles indicate the risk zones A, B, and C, respectively). B) [inset], radar satellite image of the conflux of the Labe and Vltava Rivers on August 17, 2002 (2 days after the flood culmination), showing extent of floodwater (dark areas). Inundated forests, with subsequent mass occurrences of Ochlerotatus and Aedes mosquitoes, are visible as lighter areas surrounding Labe River upstream of the confluence; scattered lagoons (dark areas) in arable fields along both rivers far left and right turned into breeding sites of predominantly Culex mosquitoes. We subdivided the flooded area into 4 risk zones according to quantities of mosquitoes. Zone A was a forested floodplain along the Labe River between Obříství-Kly and Lobkovice-Kozly (11 villages), with large quantities of mosquitoes. Zone B was an intermediate area between zones A and C (5 villages, 1 small town), with fewer breeding sites but possibility for mosquito migration from zone A. Zone C was the area along the Vltava and Labe Rivers between Kralupy and Horní Počaply (25 villages and small towns), with no floodplain forests and few breeding sites for mosquitoes. Zone D was a control zone, with only sporadic occurrences of mosquitoes (mainly in Prague). Informed written consent and serum samples were obtained from 497 survey participants of various ages from September 6 to September 13, 2002 (3 weeks after the flood culmination and 2 weeks after the mosquito emergence). Paired serum samples were taken from 150 of the survey participants 6 months later, from April 9 to May 15, 2003 (34 in zone A, 43 in zone B, 73 in zone C). Serologic examination was performed with the hemagglutination-inhibition (HIT) and plaque-reduction neutralization tests (PRNT) in microplates (–). The strains used for HIT were TAHV 92, WNV Eg101, BATV 184, and SINV Eg339; a commercial control antigen (Test-Line Ltd., Brno, Czech Republic) of Central European tickborne encephalitis virus (CEEV) was used. All serum samples were acetone-extracted and tested with sucrose- and acetone-processed antigens by using 8 hemagglutinin units; titers >20 were considered positive. For PRNT, TAHV T16, WNV Eg101, CEEV Hypr, and BATV, 184 viral strains were used. The test was conducted on Vero or SPEV (embryonic pig kidney: for CEEV) cells. All serum samples were heat inactivated and screened for antibodies at 1:8; those reducing the number of virus plaques by 90% were considered positive and titrated to estimate dilutions causing plaque–number reduction by 50% (PRNT50) and 90% (PRNT90). The serum samples reacting with WNV were examined for cross-reactivity with CEEV. PRNT with BATV was used only as a confirmatory test for the serum samples reacting with BATV in HIT. Against TAHV, 82 (16.5%) of 497 study participants had neutralizing antibodies, and 74 (14.9%) were seropositive in HIT. In PRNT50, the titers were 32–2048 (geometric mean titer [GMT] 260), in PRNT90 16–1024 (GMT 119), and in HIT 20–40 to 160 (GMT 40). Figure 2 illustrates the distribution of neutralizing antibody titers. No difference occurred in neutralizing antibody prevalence between sexes, 32 (15.8%) of 202 males and 50 (16.9%) of 295 females (χ2 = 0.11; p = 0.744). The prevalence rate increased significantly with age (Table 1: χ2 = 39,809; p <0.001); TAHV antibodies were found infrequently in persons <19 years of age. Neutralizing antibody distribution, with respect to the residence location (Table 2, Figure 1), showed the highest seroprevalence in zone A (28%), lower seroprevalences in zones B and C, and 5% in the control zone D (χ2 = 14.57; p = 0.002). Significant differences were found between zone D and all other zones, and between zones A and C (χ2 = 7.243; p = 0.007), but not between zones A and B or B and C; HIT yielded similar results. The seroprevalence in relation to the proximity of study participants’ locations to the nearest floodplain forest within zones A, B, and C demonstrated decreasing seroprevalence with increasing proximity to the forest (χ2 = 8.51; p = 0.003) (Table 2).
Figure 2

Distribution of 50% plaque-reduction neutralization titers of antibodies to Tahyna virus (y axis, number of seroreactors).

Table 1

Comparison of the prevalence of neutralizing antibodies to Tahyna virus by age groups after the floods in central Bohemia in 2002 and southern Moravia in 1997*†

Age (y)CB 2002, n% positiveSM 1997, n% positive
0–9185.6390.0
10–19530.0498.2
20–29745.412819.5
30–396917.47963.3
40–496211.38062.5
50–598619.89081.1
60–697832.15979.7
>705728.19588.4

*CB, central Bohemia; SM, southern Moravia; n, number of residents examined.
†Source (6).

Table 2

Prevalence of neutralizing antibodies to Tahyna virus after the 2002 flood, Central Bohemia*

 n†% positive
Risk zone
A7528.0
B8320.5
C27914.7
D605.0
Distance to FPF (km)
<1.07828.2
1.0–2.97521.3
3.0–5.97017.1
≥6.021413.6

*As related to the residence location: risk zones A to D; and distance to floodplain forest (FPF, within zones A, B, and C only).
†n, number of residents examined.

Distribution of 50% plaque-reduction neutralization titers of antibodies to Tahyna virus (y axis, number of seroreactors). *CB, central Bohemia; SM, southern Moravia; n, number of residents examined.
†Source (6). *As related to the residence location: risk zones A to D; and distance to floodplain forest (FPF, within zones A, B, and C only).
†n, number of residents examined. Against WNV, no specific reactions were found. Although serum samples from 34 (6.8%) study participants reacted in HIT with the WNV at titers 40 to 80, all of them also reacted with CEEV at titers similar or higher (≤160). CEEV could have occurred in the area, and some study participants may have been vaccinated against tickborne encephalitis. In PRNT90, 6 study participants (1.2%) reacted with WNV but at low titers of 8 to 16; these serum samples also reacted in PRNT with CEEV; thus, the results were considered to be crossreactions as well. Additionally, 42 (8.5%) seroreactors against WNV appeared in the less stringent PRNT50, but all titers were low (8–32) and cross-reacted with CEEV. Against SINV, antibodies were tested with HIT only and detected in specimens from 7 (1.4%) study participants, with low titers of 20 to 40. Of the BATV, specimens from 7 study participants reacted in HIT at a low titer of 20. By confirmatory testing of these serum samples in PRNT, only 1 (0.2%) showed specific antibodies to BATV; the titer was 64 in PRNT50 and 32 in PRNT90. Seroconversion (>4-fold rise in titer) was found with TAHV only. After the flood the infection episode occurred in one 55-year-old woman from Obříství (zone A), as shown by the seroconversion in both HIT (<20/40) and PRNT50 (<8/512). Three other study participants seroconverted in 1 test only: a 40-year-old man from Chlumín, zone B (HIT 20/80; PRNT 128/128); a 32-year-old man from Chlumín (HIT <20/20–40; PRNT 128/64); and an 80-year-old woman from Obříství (HIT 20/80; PRNT 64/32). These results are less convincing. Upon our request, local general practitioners did not corroborate consistent signs of a disease reported by these 4 study participants from October 2002 to April 2003. In general, clinical symptoms of TAHV infection are milder in adults than in children (). Seroconversion against mosquitoborne viruses was not detected in any of the 73 study participants in zone C.

Conclusions

On the basis of this serosurvey, recent infections with WNV (in contrast to South Moravia after the 1997 flood (,), SINV, and BATV have not been found in Central Bohemia after the flood. However, activity of another mosquitoborne virus, TAHV, has been found in a natural focus along the Labe River at Neratovice. This focus has so far gone unnoticed (). Lower frequency of TAHV antibodies has been detected along the lower reaches of the Vltava River. The prevalence of antibodies to TAHV increased with risk-zone ranking (from zone D to the highest risk zone A) and with decreasing distance to floodplain forests, the primary breeding habitat of vector mosquitoes (–). In disease-endemic areas, the proportion of residents with antibodies against California group viruses increase with age (,). A similar situation occurred in the Central Bohemian flooded area, where antibodies to TAHV were detected in a low proportion of residents <20 years of age. Nevertheless, TAHV seems to be active in the area. At least 1 seroconversion among 150 residents (attack rate ≈0.67%) against TAHV has been proven. With ≈100,000 inhabitants in the risk zones (1992 census), ≈670 (95% confidence interval 20–3,719) persons could have been infected after the flood. Environmental factors, such as heavy rains followed by a flood, artificial inundation of floodplain forests, or rehabilitation of wetlands that support mosquito-vector populations, could give rise to preconditions for an increased incidence of mosquitoborne infectious diseases, even in temperate climates. Under such circumstances, the optimum strategy is an epidemiologic surveillance that includes monitoring, especially of infection rate of mosquito populations and incidence of mosquitoborne diseases in humans. The surveillance results could then be used in integrated mosquito control.
  9 in total

1.  THE ISOLATION OF THE TAHY NA VIRUS FROM THE MOSQUITO AUEDES VEXANS IN SOUTHERN MORAVIA.

Authors:  J M KOLMAN; D MALKOVA; A NEMEC; A SMETANA; Z HAJKOVA; J MINAR
Journal:  J Hyg Epidemiol Microbiol Immunol       Date:  1964

2.  Techniques for hemagglutination and hemagglutination-inhibition with arthropod-borne viruses.

Authors:  D H CLARKE; J CASALS
Journal:  Am J Trop Med Hyg       Date:  1958-09       Impact factor: 2.345

3.  Dynamics of the natural focus of Tahyna virus in southern Moravia and species succession of its vectors, the mosquitoes of the genus Aedes.

Authors:  V Danielová; D Málková; J Minár; J Ryba
Journal:  Folia Parasitol (Praha)       Date:  1976       Impact factor: 2.122

4.  Isolation of Tahyna virus from the blood of sick children.

Authors:  V Bárdos; M Medek; V Kania; Z Hubálek
Journal:  Acta Virol       Date:  1975-09       Impact factor: 1.162

5.  [Incidence of antibodies against Tahyna, Calovo and tick-borne encephalitis viruses in the population of Bohemia. 1. Elbe Basin].

Authors:  J M Kolman; K Kopecký; J Minár; M Hausenblasová
Journal:  Cesk Epidemiol Mikrobiol Imunol       Date:  1972-03

6.  The flaviviruses (group B arboviruses): a cross-neutralization study.

Authors:  A T De Madrid; J S Porterfield
Journal:  J Gen Virol       Date:  1974-04       Impact factor: 3.891

7.  West Nile virus investigations in South Moravia, Czechland.

Authors:  Z Hubálek; H M Savage; J Halouzka; Z Juricová; Y O Sanogo; S Lusk
Journal:  Viral Immunol       Date:  2000       Impact factor: 2.257

8.  [Surveillance of mosquito-borne viruses in Breclav after the flood of 1997].

Authors:  Z Hubálek; J Halouzka; Z Juricová; Z Príkazský; J Záková; O Sebesta
Journal:  Epidemiol Mikrobiol Imunol       Date:  1999-08       Impact factor: 0.444

9.  Seroepidemiology of La Crosse virus infection in humans in western North Carolina.

Authors:  D E Szumlas; C S Apperson; P C Hartig; D B Francy; N Karabatsos
Journal:  Am J Trop Med Hyg       Date:  1996-04       Impact factor: 2.345

  9 in total
  17 in total

1.  The Presence and Seroprevalence of Arthropod-Borne Viruses in Nasiriyah Governorate, Southern Iraq: A Cross-Sectional Study.

Authors:  Ali Mohammed Barakat; Teemu Smura; Suvi Kuivanen; Eili Huhtamo; Satu Kurkela; Niina Putkuri; Hassan J Hasony; Haider Al-Hello; Olli Vapalahti
Journal:  Am J Trop Med Hyg       Date:  2016-02-15       Impact factor: 2.345

2.  Possible ecology and epidemiology of medically important mosquito-borne arboviruses in Great Britain.

Authors:  J M Medlock; K R Snow; S Leach
Journal:  Epidemiol Infect       Date:  2006-08-08       Impact factor: 2.451

3.  Evidence of Apeu Virus Infection in Wild Monkeys, Brazilian Amazon.

Authors:  Danilo B Oliveira; Ana Paula Moreira Franco Luiz; Alexandre Fagundes; Carla Amaral Pinto; Cláudio A Bonjardim; Giliane S Trindade; Erna G Kroon; Jônatas S Abrahão; Paulo C P Ferreira
Journal:  Am J Trop Med Hyg       Date:  2016-01-19       Impact factor: 2.345

4.  Circulation of diverse genotypes of Tahyna virus in Xinjiang, People's Republic of China.

Authors:  Zhi Lu; Shi-Hong Fu; Feng-Tian Wang; Roger S Nasci; Qing Tang; Guo-Dong Liang
Journal:  Am J Trop Med Hyg       Date:  2011-09       Impact factor: 2.345

5.  Tahyna virus genetics, infectivity, and immunogenicity in mice and monkeys.

Authors:  Richard S Bennett; Anthony K Gresko; Brian R Murphy; Stephen S Whitehead
Journal:  Virol J       Date:  2011-03-24       Impact factor: 4.099

Review 6.  Newly recognized mosquito-associated viruses in mainland China, in the last two decades.

Authors:  Hong Liu; Xiaoyan Gao; Guodong Liang
Journal:  Virol J       Date:  2011-02-14       Impact factor: 4.099

Review 7.  Factors increasing vulnerability to health effects before, during and after floods.

Authors:  Dianne Lowe; Kristie L Ebi; Bertil Forsberg
Journal:  Int J Environ Res Public Health       Date:  2013-12-11       Impact factor: 3.390

Review 8.  Examining the relationship between infectious diseases and flooding in Europe: A systematic literature review and summary of possible public health interventions.

Authors:  Lisa Brown; Virginia Murray
Journal:  Disaster Health       Date:  2013-04-01

Review 9.  Viral zoonoses in Europe.

Authors:  Hannimari Kallio-Kokko; Nathalie Uzcategui; Olli Vapalahti; Antti Vaheri
Journal:  FEMS Microbiol Rev       Date:  2005-06-29       Impact factor: 16.408

10.  Tahyna virus and human infection, China.

Authors:  Zhi Lu; Xin-Jun Lu; Shi Hong Fu; Song Zhang; Zhao Xia Li; Xin Hua Yao; Yu Ping Feng; Amy J Lambert; Da Xin Ni; Feng Tian Wang; Su Xiang Tong; Roger S Nasci; Yun Feng; Qiang Dong; You Gang Zhai; Xiao Yan Gao; Huan Yu Wang; Qing Tang; Guo Dong Liang
Journal:  Emerg Infect Dis       Date:  2009-02       Impact factor: 6.883

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.