Mycoplasma hyorhinis
(Switzer, 1955)
Etymology
Gr. n. mukes – fungus, Gr. neut. n. plasma – anything formed, N.L. neut. n. Mycoplasma – fungus form; Gr. n. hus – a swine, Gr. n. rhis – nose, N.L. gen. n. hyorhinis – of the nose of a swine
Taxonomy
Mycoplasmatales – Mycoplasmataceae – Mycoplasma – Mycoplasma hyorhinis (Hyopneumoniae cluster), separated branch, related to Mycoplasma conjunctivae (16S rRNA gene sequence similarity – 93.37%) (Fig. 1)
Type strain
BTS-7T (swine, USA, ≤1955) (Fig. 2, 16S rRNA gene sequence)
Genomes
10 completed (2x PG42T – USA; HUB-1 – China; SK76 – USA; 2 x GDL-1 cell culture isolate– origin undefined; MCLD cell culture isolate – Israel; DBS 1050 cultivar α cell culture isolate – origin undefined; MDBK-IBV cell culture isolate – Brazil; JF5820 - Switzerland; 4236J19c, 4453J21c, 4455N20c, N36N21c – Austria; Nahrain cell culture isolate – Iraq); 85 draft genomes (NCBI Genome deposit per 11/05/2024)
Cell morphology
spherical – coccoid
Colony morphology
fried egg morphology, variable in size and in opacity (Fig. 3)
Metabolism
fermentation of glucose; assimilation of glycerol; non-arginine-hydrolyzing, non-urea-hydrolyzing
Host
swine
Habitat
upper respiratory tract
Disease(s)
polyserositis and arthritis in postweaning pigs under ten weeks of age, probably involved in PRDC and MIRD, occasionally reported to cause conjunctivitis, otitis and meningoencephalitis
Pathogenicity
factors largely unknown, known factors include a family of phase- and size-variable membrane surface lipoproteins (Vlp’s) with roles in adhesion and immune evasion, cell invasion, hydrogen peroxide production via glycerol assimilation, methylation of host cell DNA (via DNA-methyltransferases)
Epidemiology
worldwide occurrence in swine, common contaminant of cell cultures; transmission via sow-piglet contact, rapid spread in postweaning pigs
Diagnosis
cultivation and species identification by MALDI-ToF MS, serology or genetically; PCR
Fig. 1. Maximum likelihood tree showing the phylogenetic position of Mycoplasma hyorhinis BTS7T within the Hyopneumoniae cluster of Mycoplasmataceae based on 16S rRNA gene sequences. The sequence of Mycoplasma synoviae WVU 1853T was used as out-group (Synoviae cluster). Numbers at nodes represent bootstrap confidence values (1000 replications). Only values > 80% are shown. Bar, number of substitutions per nucleotide position. Credits: Joachim Spergser (Vetmeduni Vienna)
CTCGCTGTGTGCCTAATACATGCATGTTGAACGGGATGTAGCAATACATTCAGTAGCGAATGGGTGAGTAACACGTACCTAACCTACCTTTAAGACTGGGATAACTATTGGAAACAATAGCTAATACCGGATATAGTTATTTATCGCATGATGAGTAATAGAAAGGAGCTTCACAGCTTCACTTAAAAATGGGGGTGCGGAACATTAGTTAGTTGGTAGGGTAATGGCCTACCAAGACGATGATGTTTAGCCGGGCCGAGAGGCTGTACGGCCACACTGGGACTGAGATACGGCCCAGACTCCTACGGGAGGCAGCAGTAAGGAATTTTCCACAATGAGCGAAAGCTTGATGGAGCGACACAGCGTGCAGGATGAAGTTCTTCGGAATGTAAACTGCTGTTATAAGGGAAGAAAAAATAGAATAGGAAATGATTTTATCTTGACGGTACCTTATTAGAAAGCGACGGCAAACTATGTGCCAGCAGCCGCGGTAATACATAGGTCGCAAGCGTTATCCGGAATTATTGGGCGTAAAGCGTCCGTAGGTTTTTTGCTAAGTCTGGAGTTAAATGCTGAAGCTCAACTTCAGTCCGCTTTGGATACTGGCAAAATAGAATTATAAAGAGGTTAGCGGAATTCCTAGTGAAGCGGTGGAATGCGTAGATATTAGGAAGAACACCAATAGGCGAAGGCAGCTAACTGGTTATATATTGACACTAAGGGACGAAAGCGTGGGGAGCAAACAGGATTAGATACCCTGGTAGTCCACGCCGTAAACGATGATCATTAGTTGGTGGAATAATTTCACTAACGCAGCTAACGCGTTAAATGATCCGCCTGAGTAGTATGCTCGCAAGAGTGAAACTTAAAGGAATTGACGGGAACCCGCACAAGCGGTGGAGCATGTGGTTTAATTTGAAGATACGCGTAGAACCTTACCCACTCTTGACATCTTCTGCAAAGCTATAGAGATATAGTGGAGGTTAACAGAATGACAGATGGTGCATGGTTGTCGTCAGCTCGTGTCGTGAGATGTTAGGTTAAGTCCTGCAACGAGCGCAACCCTTTTCTTTAGTTACTAATATTAAGTTAAGGACTCTAGAGATACTGCCTGGGTAACCAGGAGGAAGGTGGGGACGACGTCAAATCATCATGCCTCTTACGAGTGGGGCAACACACGTGCTACAATGGTCGGTACAAAGAGAAGCAATATGGTGACATGGAGCAAATCTCAAAAAACCGATCTCAGTTCGGATTGAAGTCTGCAACTCGACTTCATGAAGTCGGAATCGCTAGTAATCGTAGATCAGCTACGCTACGGTGAATACGTTCTCGGGTTTTGTACACACCGCCCGTCACACCATGGGAGTTGGTAATGCCCAAAGTCGGTGAGTTAACTTCGGAGACCATTGCCTAAGGCAGGACTGATGACTGGGGTGAAGTCGTAACAAGGT
Fig. 2. 16S rRNA gene sequence of Mycoplasma hyorhinis BTS-7T (Accession number: NR_041845)Fig. 3. Colonies of Mycoplasma hyorhinis BTS-7T on modified Hayflick’s agar after 5 days of incubation exhibiting fried egg morphology and variability in size and in opacity. Bar, 1 mm. Credits: Joachim Spergser (Vetmeduni Vienna)