1
Possible range expansion of the yellow fever mosquito in Palm Beach County, Florida Kristen A. Hopperstad and Michael H. Reiskind • Department of Entomology, North Carolina State University, Raleigh, NC Abstract Introduction Methods Results & Discussion References [1] Reiskind MH, Westbrook CJ, Lounibox LP. 2010. Exposure to chikungunya virus and adult longevity in Aedes aegypti (L.) and Aedes albopictus (Skuse). Journal of Vector Ecology 35(1) 61-68 [2] O’Meara GF, Evans LF, Gettman AD, Cuda JP. 1995. Spread of Aedes albopictus and Decline of Ae. aegypti (Diptera: Culicidae) in Florida. Journal of Medical Entomology 32(4) 554- 562 [3] Reiskind MH, Lounibos LP. 2013. Spatial and temporal patterns of abundance of Aedes aegypti L. (Stegomyia aegypti) and Aedes albopictus (Skuse) [Stegomyia albopictus (Skuse)] in southern Florida. Medical and Veterinary Entomology 27(4) 421-429 [4] Braks MAH, Honorio NA, Lourenco-De-Oliveira R, Juliano SA, Lounibos LP. 2003. Convergent Habitat Segregation of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Southeastern Brazil and Florida. Journal of Medical Entomology 40(6): 785-594 [5] Terando AJ, Costanza J, Belyea C, Dunn RR, McKerrow A, Collazo JA. 2014. The Southern Megalopolis: Using the Past to Predict the Future of Urban Sprawl in the Southeast U.S. PLoS ONE 9(7) 1-8 Acknowledgements This material is based upon work supported by the National Science Foundation Graduate Research Fellowship under Grant No. (DGE-1252376). We thank the University of Florida Medical Entomology Laboratory for use of their facility, Dr. Phil Lounibos for acting as our host PI in Florida, and undergraduate technical assistance for this project. Disease transmission is directly tied to the spatial distribution of disease vectors. The distribution of Aedes aegypti in the United States has diminished since the introduction of Aedes albopictus in the 1980s; however, Ae. aegypti persists in some urban areas, particularly in south Florida. We studied the spatial patterning of Ae. aegypti at a fine landscape scale by comparing the distribution of Ae. aegypti in Palm Beach County, Florida from 2006-7 to the distribution from 2013, taking into account microclimate and land cover. We found landscape and microclimate factors help explain the distribution of the two mosquitoes with evidence for a local range shift of Ae. aegypti. This local change in distribution may have implications for shifts on a much broader scale, with concomitant changes in risk of disease transmission. Sampling Methods We collected mosquito eggs at sites previously sampled in 2006 and 2007 3 (Fig. 1). Sites were located along 6 latitudinal transects that followed a coastal+urban to inland+rural gradient. Sites were located at 0, 1, 3, 8, & 15 km from the coast. We placed 3 oviposition traps at each site and serviced traps on a weekly basis for 6 weeks (Fig. 2). iButton data loggers recorded temperature and RH for at least 3 weeks at every site. Eggs were reared from one positive trap per site per week (Fig. 3); up to 30 eggs were reared from a single trap. Mosquitoes were identified to species at the pupal stage. Landscape Digitization We classified land cover within 100 m of each site using Esri ArcMap 10.2.2 for years high resolution orthoimagery was available: 2006 and 2013. Polygons were drawn over orthoimagery (0.15-0.5 m resolution) and categorized as: bare ground, building, coarse or fine vegetation, freshwater, saltwater, pool, or pavement. Statistics Using JMP 11.2, linear regressions related abundance, landscape, and climate to distance. The proportion of Ae. aegypti for each year was compared using a Wilcoxon Signed Rank test, and an ANOVA and Tukey’s HSD test. Figure 2. Oviposition trap in field. Oviposition traps were lined with paper and baited with 5 g/L unsterile oak leaf infusion. An ibutton was affixed to the bottom of one trap per site. Aedes aegypti is responsible for recent dengue outbreaks in the U.S. and is the most important vector for the emerging chikungunya virus. 1 Although once widespread, Aedes aegypti declined in the U.S. after the invasion of Aedes albopictus in the 1980s. 2 Aedes aegypti persists however, mostly restricted to urban enclaves. 2,3 Habitat segregation can explain this persistence, as Ae. aegypti thrives in dry, hot urban areas compared to Ae. albopictus. 4 Aedes aegypti persistence is troublesome because its suitable habitat is expected to double or triple within the next 50 years due to increasing urban sprawl and climate change. 5 Landscape, climate, and/or adaptive change have the potential to allow the expansion of Ae. aegypti distributions. Objective: To compare 2006, 2007, and 2013 Aedes aegypti distributions, taking into account landscape and microclimate. For all years, linear regressions show Ae. aegypti abundance was negatively correlated with distance from the coast; Ae. albopictus was positively correlated (Fig. 4) A Wilcoxon Signed Rank test showed a significant increase in the proportion of Ae. aegypti at 8 km in 2013 compared to 2006 and 2007, and a non-significant negative trend at 1 km from 2007 to 2013 (Table 1). The proportion of Ae. aegypti increased at 8 km, possibly indicating a recent increase in spatial distribution (Fig. 5). Further analyses will examine relationships between climate, landscape, and Ae. aegypti distributions. Currently these and additional data are being analyzed on a broader scale in a more rigorous landscape analysis, and an ongoing population genetic study will measure gene flow and characterize the population structure of Ae. aegypti in the southeastern U.S. Figure 3. Aedes rearing containers. Eggs and larvae were reared in 200 mL tap water, 100 mL unsterile oak leaf infusion, 0.03 g Brewer’s yeast, and 0.03 g powdered egg yolk or Bacto TC lactalbumin. Insert shows upclose view of a rearing container. Figure 1. Collection sites in Palm Beach County, Florida. Sites are represented by yellow circles and are shown within the state of Florida and at a closer view. Green areas represent vegetative cover, and grey areas represent urban cover. Base map data was obtained from the Florida Cooperative Land Cover Map and re-symbolized (Florida Fish and Wildlife Conservation Commission and Florida Natural Areas Inventory. 2014. Cooperative Land Cover version3.0 Vector. Tallahassee, FL). Mean proportion of Ae. aegypti by year and distance from the coast Figure 5. Mean proportion Ae. aegypti in 2006, 2007, and 2013. Blue bars represent 2006, green represents 2007, and yellow represents 2013. Each error bar is constructed using 1 standard error from the mean. Abundance at 8 km is higher in 2013 than in 2006 and 2007 (corrected p=0.0413, corrected p=0.0212, respectively, ANOVA and Tukey’s HSD). Distance from the coast (KM) Mean # Ae. aegypti/total mosquitoes 2013 2007 2006 Table 1. Results from Wilcoxon Signed Rank test, showing sample size (N), test statistic (S), and significance (ns = not significant) of paired comparisons (by site) of percent Ae. aegypti at different distances from the coast. Significance was assessed with a two-tailed alpha of 0.05. Tied percent Ae. aegypti in different years were not ranked. The only significant comparisons are between 2013 versus 2006 and 2007 at 8 km inland. Every site at 8 km inland had a higher percentage of Ae. aegypti in 2013 than in 2006 or 2007. Comparison Distance from Coast 2006 v 2007 2006 v 2013 2007 v 2013 0 N= 6, S=2.5, ns N=6, S=5.5, ns N=3, S=0, ns 1 N=5, S=4.5, ns N=5, S=-0.5, ns N=5, S=-7.5, p<0.10 3 N=6, S=0.5, ns N=6, S=4.5, ns N=6, S=1.5, ns 8 N=5, S=-2.5, ns N=6, S=10.5, p<0.05 N=6, S=10.5, p<0.05 15 N=6, S=-0.5, ns N=6, S=6.5, ns N=5, S=1.5, ns Proportion Ae. aegypti and Ae. albopictus across landscape & time Figure 4. Proportion of Ae. aegypti and Ae. albopictus in 2006, 2007, and 2013. Each pie chart represents a collection site. Yellow represents Ae. aegypti and blue represents Ae. albopictus. Avg daily temperature decreased and avg daily RH increased with distance from the coast. At 15 km, temperature was lower in 2013 than in 2006 (p=0.0139); no other changes in microclimate were significant. At 15 km, bare ground decreased from 2006 to 2013 (p < 0.05); no other changes in land cover were significant. Aedes aegypti Aedes albopictus 2006 2007 2013

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Page 1: Possible range expansion of the yellow fever mosquito in Palm …vectorecology.org/wp-content/uploads/AMCA_poster_final.pdf · Possible range expansion of the yellow fever mosquito

Possible range expansion of the yellow fever mosquito in Palm Beach County, FloridaKristen A. Hopperstad and Michael H. Reiskind • Department of Entomology, North Carolina State University, Raleigh, NC

Abstract

Introduction

Methods

Results & Discussion

References

[1] Reiskind MH, Westbrook CJ, Lounibox LP. 2010. Exposure to chikungunya virus and adult longevity in Aedes aegypti (L.)

and Aedes albopictus (Skuse). Journal of Vector Ecology 35(1) 61-68 [2] O’Meara GF, Evans LF, Gettman AD, Cuda JP. 1995.

Spread of Aedes albopictus and Decline of Ae. aegypti (Diptera: Culicidae) in Florida. Journal of Medical Entomology 32(4) 554-

562 [3] Reiskind MH, Lounibos LP. 2013. Spatial and temporal patterns of abundance of Aedes aegypti L. (Stegomyia aegypti)

and Aedes albopictus (Skuse) [Stegomyia albopictus (Skuse)] in southern Florida. Medical and Veterinary Entomology 27(4)

421-429 [4] Braks MAH, Honorio NA, Lourenco-De-Oliveira R, Juliano SA, Lounibos LP. 2003. Convergent Habitat Segregation

of Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Southeastern Brazil and Florida. Journal of Medical Entomology

40(6): 785-594 [5] Terando AJ, Costanza J, Belyea C, Dunn RR, McKerrow A, Collazo JA. 2014. The Southern Megalopolis:

Using the Past to Predict the Future of Urban Sprawl in the Southeast U.S. PLoS ONE 9(7) 1-8

Acknowledgements

This material is based upon work supported by the National Science Foundation Graduate

Research Fellowship under Grant No. (DGE-1252376). We thank the University of Florida

Medical Entomology Laboratory for use of their facility, Dr. Phil Lounibos for acting as our host

PI in Florida, and undergraduate technical assistance for this project.

Disease transmission is directly tied to the spatial distribution of disease

vectors. The distribution of Aedes aegypti in the United States has

diminished since the introduction of Aedes albopictus in the 1980s; however,

Ae. aegypti persists in some urban areas, particularly in south Florida. We

studied the spatial patterning of Ae. aegypti at a fine landscape scale by

comparing the distribution of Ae. aegypti in Palm Beach County, Florida from

2006-7 to the distribution from 2013, taking into account microclimate and

land cover.

We found landscape and microclimate factors help explain the distribution of

the two mosquitoes with evidence for a local range shift of Ae. aegypti. This

local change in distribution may have implications for shifts on a much

broader scale, with concomitant changes in risk of disease transmission.

Sampling MethodsWe collected mosquito eggs at sites previously sampled in 2006 and 20073 (Fig. 1). Sites

were located along 6 latitudinal transects that followed a coastal+urban to inland+rural

gradient. Sites were located at 0, 1, 3, 8, & 15 km from the coast.

We placed 3 oviposition traps at each site and serviced traps on a weekly basis for 6 weeks

(Fig. 2). iButton data loggers recorded temperature and RH for at least 3 weeks at every site.

Eggs were reared from one positive trap per site per week (Fig. 3); up to 30 eggs were reared

from a single trap. Mosquitoes were identified to species at the pupal stage.

Landscape DigitizationWe classified land cover within 100 m of each site using Esri ArcMap 10.2.2 for years high

resolution orthoimagery was available: 2006 and 2013. Polygons were drawn over

orthoimagery (0.15-0.5 m resolution) and categorized as: bare ground, building, coarse or

fine vegetation, freshwater, saltwater, pool, or pavement.

StatisticsUsing JMP 11.2, linear regressions related abundance, landscape, and climate to distance.

The proportion of Ae. aegypti for each year was compared using a Wilcoxon Signed Rank

test, and an ANOVA and Tukey’s HSD test.

Figure 2. Oviposition trap in field. Oviposition

traps were lined with paper and baited with 5

g/L unsterile oak leaf infusion. An ibutton was

affixed to the bottom of one trap per site.

Aedes aegypti is responsible for recent dengue outbreaks in the U.S. and

is the most important vector for the emerging chikungunya virus. 1

Although once widespread, Aedes aegypti declined in the U.S. after the

invasion of Aedes albopictus in the 1980s.2

Aedes aegypti persists however, mostly restricted to urban enclaves.2,3

Habitat segregation can explain this persistence, as Ae. aegypti thrives in

dry, hot urban areas compared to Ae. albopictus.4

Aedes aegypti persistence is troublesome because its suitable habitat is

expected to double or triple within the next 50 years due to increasing

urban sprawl and climate change.5

Landscape, climate, and/or adaptive change have the potential to allow the expansion of Ae. aegypti distributions.

Objective: To compare 2006, 2007, and 2013 Aedes aegypti

distributions, taking into account landscape and microclimate.

For all years, linear regressions show

Ae. aegypti abundance was negatively

correlated with distance from the coast;

Ae. albopictus was positively correlated (Fig. 4)

A Wilcoxon Signed Rank test showed a

significant increase in the proportion of

Ae. aegypti at 8 km in 2013 compared to 2006

and 2007, and a non-significant negative trend

at 1 km from 2007 to 2013 (Table 1).

The proportion of Ae. aegypti increased at 8 km,

possibly indicating a recent increase in spatial

distribution (Fig. 5). Further analyses will

examine relationships between climate,

landscape, and Ae. aegypti distributions.

Currently these and additional data are being

analyzed on a broader scale in a more rigorous

landscape analysis, and an ongoing population

genetic study will measure gene flow and

characterize the population structure of

Ae. aegypti in the southeastern U.S.

Figure 3. Aedes rearing containers. Eggs and larvae

were reared in 200 mL tap water, 100 mL unsterile oak

leaf infusion, 0.03 g Brewer’s yeast, and 0.03 g

powdered egg yolk or Bacto TC lactalbumin. Insert

shows upclose view of a rearing container.

Figure 1. Collection sites in Palm Beach County, Florida. Sites are represented by yellow circles and

are shown within the state of Florida and at a closer view. Green areas represent vegetative cover,

and grey areas represent urban cover. Base map data was obtained from the Florida Cooperative

Land Cover Map and re-symbolized (Florida Fish and Wildlife Conservation Commission and Florida

Natural Areas Inventory. 2014. Cooperative Land Cover version3.0 Vector. Tallahassee, FL).

Mean proportion of Ae. aegypti by

year and distance from the coast

Figure 5. Mean proportion Ae. aegypti in 2006, 2007, and

2013. Blue bars represent 2006, green represents 2007, and

yellow represents 2013. Each error bar is constructed using 1

standard error from the mean. Abundance at 8 km is higher in

2013 than in 2006 and 2007 (corrected p=0.0413, corrected

p=0.0212, respectively, ANOVA and Tukey’s HSD).

Distance from the coast (KM)

Mean #

Ae. aegypti/t

ota

l m

osquitoes

201320072006

Table 1. Results from Wilcoxon Signed Rank test, showing sample size (N), test statistic (S), and significance

(ns = not significant) of paired comparisons (by site) of percent Ae. aegypti at different distances from the coast.

Significance was assessed with a two-tailed alpha of 0.05. Tied percent Ae. aegypti in different years were not

ranked. The only significant comparisons are between 2013 versus 2006 and 2007 at 8 km inland. Every site at 8 km

inland had a higher percentage of Ae. aegypti in 2013 than in 2006 or 2007.

Comparison

Distance from Coast 2006 v 2007 2006 v 2013 2007 v 2013

0 N= 6, S=2.5, ns N=6, S=5.5, ns N=3, S=0, ns

1 N=5, S=4.5, ns N=5, S=-0.5, ns N=5, S=-7.5, p<0.10

3 N=6, S=0.5, ns N=6, S=4.5, ns N=6, S=1.5, ns

8 N=5, S=-2.5, ns N=6, S=10.5, p<0.05 N=6, S=10.5, p<0.05

15 N=6, S=-0.5, ns N=6, S=6.5, ns N=5, S=1.5, ns

Proportion Ae. aegypti and Ae. albopictus across landscape & time

Figure 4. Proportion of Ae. aegypti and Ae. albopictus in 2006, 2007, and 2013. Each

pie chart represents a collection site. Yellow represents Ae. aegypti and blue represents

Ae. albopictus. Avg daily temperature decreased and avg daily RH increased with

distance from the coast. At 15 km, temperature was lower in 2013 than in 2006

(p=0.0139); no other changes in microclimate were significant. At 15 km, bare ground

decreased from 2006 to 2013 (p < 0.05); no other changes in land cover were significant.

Legend

PBCsites

AegCollected

AlboCollected

Aedes aegypti

Legend

PBCsites

AegCollected

AlboCollectedAedes albopictus

2006 2007 2013