Oligochaete worms without any
mouth, gut, or
nephridial excretory system were first discovered in the 1970s-1980s near
Bermuda. They were later found to contain symbiotic
chemosynthetic bacteria which serve as their primary food source.
O. algarvensis is the species where this symbiosis has been studied in the most detail. There are five different species of bacterial
symbionts in
O. algarvensis, which are located under the cuticle of the worm: two
sulfide-oxidizing Gammaproteobacteria, two
sulfate-reducing Deltaproteobacteria, and one
spirochaete. The sulfide-oxidizers gain energy from oxidation of
hydrogen sulfide, and
fix carbon dioxide via the
Calvin cycle. The sulfate-reducers are anaerobes that can reduce sulfate into sulfide, which is consumed by the sulfide-oxidizers. The metabolism of the spirochaete is unknown. Other species of
Olavius are also known to have similar symbioses with both sulfide-oxidizing and sulfate-reducing bacteria in the same worm. The primary sulfur-oxidizing symbiont, known as "Gamma1", is closely related to the primary symbionts of other species of gutless oligochaetes in the
Phallodrilinae, and also to the symbionts of nematodes in the subfamily
Stilbonematinae. In addition to hydrogen sulfide, the symbiotic bacteria also allow the worm to use
hydrogen and
carbon monoxide as energy sources, and to metabolise organic compounds like
malate and
acetate. These abilities were first discovered by sequencing the
genomes and
proteomes of the bacteria. The symbiotic bacteria which live with
O. algarvensis have other unique properties. One of the Deltaproteobacteria symbionts, called "Delta-1", is able to produce numerous seleno- and pyrroproteins, which contain the amino acids
selenocysteine and
pyrrolysine that are sometimes called the 21st and 22nd
proteinogenic amino acids. This bacterium has the largest known proteome that has seleno- and pyrroproteins. The symbionts also express the most
transposases of any known bacteria. ==References==