Abstract

Ixodes scapularis, the blacklegged deer tick, is the principal vector of Lyme disease in North America. Environmental factors are known to influence regional and seasonal incidence of Lyme disease and possibly the endemicity of the disease to the northeastern and upper mid‐western regions of the United States. With a goal to understand the impact of environmental temperature on microbial communities within the tick, we investigated the bacterial microbiome of colony‐reared I. scapularis ticks statically incubated at different temperatures (4, 20, 30, and 37°C) at a constant humidity in a controlled laboratory setting by comparison of sequenced amplicons of the bacterial 16S V4 rRNA gene to that of the untreated baseline controls. The microbiomes of colony‐reared I. scapularis males were distinct than that of females, which were entirely dominated by Rickettsia. In silico removal of Rickettsia sequences from female data revealed the underlying bacterial community, which is consistent in complexity with those seen among male ticks. The bacterial community composition of these ticks changes upon incubation at 30°C for a week and 37°C for more than 5 days. Moreover, the male ticks incubated at 30 and 37°C exhibited significantly different bacterial diversity compared to the initial baseline microbiome, and the change in bacterial diversity was dependent upon duration of exposure. Rickettsia‐free data revealed a significantly different bacterial diversity in female ticks incubated at 37°C compared to that of 4 and 20°C treatments. These results provide experimental evidence that environmental temperature can impact the tick bacterial microbiome in a laboratory setting.

Highlights

  • Ixodes scapularis is the primary North American vector of the spirochete bacterium Borrelia burgdorferi, the etiological agent of Lyme disease and the most commonly reported vectorborne illness in the United States (Burgdorfer et al, 1982; Centers for Disease Control and Prevention (CDC), 2015a, 2017a,b; Schwartz, Hinckley, Mead, Hook, & Kugeler, 2017)

  • To better understand the effects of environmental temperature on the microbial communities of ticks, we investigated the bacterial microbiomes of colony-­reared I. scapularis ticks statically incubated at different temperatures (4, 20, 30, and 37°C) at a constant relative humidity (RH) of >80% in a controlled laboratory setting, by comparison of sequenced amplicons of the hypervariable region four (V4) of the bacterial 16S rRNA gene to that of the untreated baseline controls

  • We investigated the effect of environmental temperature on the bacterial microbiome of I. scapularis ticks, the primary Lyme disease vector in North America

Read more

Summary

| INTRODUCTION

Ixodes scapularis (commonly known as the “blacklegged” or “deer” tick) is the primary North American vector of the spirochete bacterium Borrelia burgdorferi, the etiological agent of Lyme disease and the most commonly reported vectorborne illness in the United States (Burgdorfer et al, 1982; CDC, 2015a, 2017a,b; Schwartz, Hinckley, Mead, Hook, & Kugeler, 2017). The tick is a vector for a number of other human pathogens, including Anaplasma phagocytophilum, Babesia microti, and Powassan virus (CDC, 2017a; Ebel, 2010; Piesman & Eisen, 2008) These ticks carry a variety of commensal and endosymbiotic bacteria of unknown pathogenicity (Bonnet, Binetruy, Hernández-­Jarguín, & Duron, 2017; Narasimhan & Fikrig, 2015). To better understand the effects of environmental temperature on the microbial communities of ticks, we investigated the bacterial microbiomes of colony-­reared I. scapularis ticks statically incubated at different temperatures (4, 20, 30, and 37°C) at a constant relative humidity (RH) of >80% in a controlled laboratory setting, by comparison of sequenced amplicons of the hypervariable region four (V4) of the bacterial 16S rRNA gene to that of the untreated baseline controls. By day 10, only 15% of the total ticks were alive at higher temperatures (30 and 37°C combined) (see Figure 1), and we terminated the experiment by preserving all the remaining ticks at −20°C until processing

| MATERIALS AND METHODS
| DISCUSSION
Findings
| CONCLUSION
CONFLICT OF INTERESTS
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call