Abstract

Endosymbionts and intracellular parasites are common in arthropod hosts. As a consequence, (co)amplification of untargeted bacterial sequences has been occasionally reported as a common problem in DNA barcoding. While identifying amphipod species with universal COI primers, we unexpectedly detected rickettsial endosymbionts belonging to the Torix group. To map the distribution and diversity of Rickettsia species among amphipod hosts, we conducted a nationwide molecular screening of seven families of New Zealand freshwater amphipods. In addition to uncovering a diversity of Torix Rickettsia species across multiple amphipod populations from three different families, our research indicates that: (1) detecting Torix Rickettsia with universal primers is not uncommon, (2) obtaining ‘Rickettsia COI sequences’ from many host individuals is highly likely when a population is infected, and (3) obtaining ‘host COI’ may not be possible with a conventional PCR if an individual is infected. Because Rickettsia COI is highly conserved across diverse host taxa, we were able to design blocking primers that can be used in a wide range of host species infected with Torix Rickettsia. We propose the use of blocking primers to circumvent problems caused by unwanted amplification of Rickettsia and to obtain targeted host COI sequences for DNA barcoding, population genetics, and phylogeographic studies.

Highlights

  • The cytochrome c oxidase subunit 1 gene (COI), a partial fragment of mitochondrial DNA, is the marker of choice for DNA barcoding, and is widely used for population genetics and phylogeographic s­ tudies[1,2,3]

  • Our nationwide molecular screening results show that the Torix group of Rickettsia is widespread in freshwater amphipod hosts in New Zealand, and is to our knowledge the first report of Rickettsia in crustacean hosts

  • Because freshwater amphipods have limited dispersal a­ bilities[38], the widespread distribution of Torix Rickettsia in New Zealand amphipods may be explained by an ancient acquisition followed by vertical transmission, or by many independent events of recent horizontal transmission from other organisms

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Summary

Introduction

The cytochrome c oxidase subunit 1 gene (COI), a partial fragment of mitochondrial DNA, is the marker of choice for DNA barcoding, and is widely used for population genetics and phylogeographic s­ tudies[1,2,3]. This phenomenon of the amplification of non-targeted COI sequences with widely used DNA barcoding primers has already been reported. Ceccarelli et al (2016)[33] obtained COI sequences of Torix Rickettsia from six individuals of a spider species while conducting DNA barcoding, and these authors formally discussed the presence of misidentified COI sequences in GenBank. Despite these early reports, the deposition of misidentified sequences to GenBank has continued until recently. A very recent survey on BOLD reported that 0.41% of the barcode submission in BOLD are from Rickettsia, which is higher than that from Wolbachia (0.17%)[34]

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