Affiliation:
1. Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK
2. Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK
Abstract
While male-killing bacteria are known to infect across arthropods, ladybird beetles represent a hotspot for these symbioses. In some host species, there are multiple different symbionts that vary in presence and frequency between populations. To further our understanding of spatial and frequency variation, we tested for the presence of three male-killing bacteria:
Wolbachia
,
Rickettsia
and
Spiroplasma
, in two Adalia ladybird species from a previously unexplored UK population. The two-spot ladybird, A. bipunctata, is known to harbour all three male-killers, and we identified
Spiroplasma
infection in the Merseyside population for the first time. However, in contrast to previous studies on two-spot ladybirds from continental Europe, evidence from egg-hatch rates indicates the
Spiroplasma
strain present in the Merseyside population does not cause embryonic male-killing. In the related ten-spot ladybird, A. decempunctata, there is only one previous record of a male-killing symbiont, a
Rickettsia
, which we did not detect in the Merseyside sample. However, PCR assays indicated the presence of a
Spiroplasma
in a single A. decempunctata specimen. Marker sequence indicated that this
Spiroplasma
was divergent from that found in sympatric A. bipunctata. Genome sequencing of the
Spiroplasma
-infected A. decempunctata additionally revealed the presence of cobionts in the form of a Centistes parasitoid wasp and the parasitic fungi Beauveria. Further study of A. decempunctata from this population is needed to resolve whether it is the ladybird or wasp cobiont that harbours
Spiroplasma
, and to establish the phenotype of this strain. These data indicate first that microbial symbiont phenotype should not be assumed from past studies conducted in different locations, and second that cobiont presence may confound screening studies aimed to detect the frequency of a symbiont in field collected material from a focal host species.
Funder
UK Research and Innovation
Subject
Microbiology (medical),Microbiology