The disease caused by
C. psittaci, psittacosis, was first characterized in 1879 when seven individuals in Switzerland were found to experience pneumonia after exposure to tropical pet birds. The causative pathogen was not known. The related bacterial species
Chlamydia trachomatis was described in 1907, but was assumed to be a virus, as it could not be grown on artificial media. In the winter of 1929–1930, a psittacosis pandemic spread across the United States and Europe. Its mortality rate was 20% and as high as 80% for pregnant women. The disease's spread was eventually attributed to exposure to
Amazon parrots imported from Argentina. Though
C. psittaci was identified in 1930 as the agent responsible for psittacosis, it was not found to be a bacterium until examination by electron microscopy in the 1960s.
Taxonomy For several decades, the family Chlamydiaceae contained a sole genus,
Chlamydia.
C. psittaci was originally classified from the 1960s to 1999 as a species of this sole genus. In 1999, the order Chlamydiales was assigned two new families (Parachlamydiaceae and Simkaniaceae), and within the family Chlamydiaceae, the genus
Chlamydia was divided into two genera,
Chlamydia and the newly designated genus
Chlamydophila, with
C. psittaci becoming
Chlamydophila psittaci. among microbiologists, which "resulted in a reversion to the single, original genus
Chlamydia, which now encompasses all 9 species including
C. psittaci." two more were added in 2014. What were once classified as the mammal-endemic
C. psittaci abortion,
C. psittaci feline, and
C. psittaci guinea pig are since 1999 three separate species,
C. abortus,
C. felis, and
C. caviae. New species continue to be described from inside of what was thought to be
C. psittaci. Being a pathogen with a very broad host range,
C. psittaci has a lot of opportunities to recombine with other
Chlamydia. Vafin et al. (2007) believe that this intermediate position should be its own species "
C. parapsittaci", which includes the genotypes C (strains GD, CT1, Par1), D (NJ1, 92-1293, TT3, 7344/2), G (strains Rostinovo-70, 250, PP-87, KC-93), F (strains VS225, 7778B15), and non-grouped strains WC, 84/2334, and R54. Genotypes C, D, and F are isolated from avians; G is isolated from livestock abortions in the former Soviet Union; and WC was isolated from a mammal. For the Rostinovo-70 strain,
omp1,
omp2, 16S, 23S, plasmid (all partial) sequences are available. All G genotype strains have the same plasmid sequence as the one in 84/2334, and the same 23S sequence as the three strains from genotype C. Two provisional genotypes were defined in 2017: G1, G2. These too reflect an intermediate position, though because the author was unaware of Vafin's results, there was no comparison with Vafin's ompA sequences. A new species was effectively published in 2019,
C. buteonis, which consisted of one type strain RSHA from a red-shouldered hawk. This species occupies an intermediate position. Longbottom et al. (2021) sequenced the whole genome of 84/2334. They find its entire genome, alongside that of genotypes G1 and G2, to be closer to
C. abortus than to
C. psittaci, despite the fact that it has a plasmid (typical
C. abortus does not carry one). Analyses of seven MLST housekeeping gene fragments also find the same for genotype 1V, leading to the suggestion to transfer these three genotypes plus 84/2334 to
C. abortus. On the other hand,
C. buteonis was shown to be closer to
C. psittaci than to
C. abortus on MSLT, and intermediate with a long branch of its own on whole-genome NeighborNet. Vafin's four strains were not analyzed. WC and genotypes C, D, F were solidly placed in
C. psittaci. ==Diseases==