2012
DOI: 10.1128/jb.06560-11
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Genome Sequence for “Candidatus Mycoplasma haemominutum,” a Low-Pathogenicity Hemoplasma Species

Abstract: We present the genome sequence of "Candidatus Mycoplasma haemominutum" strain Birmingham 1, a low-pathogenicity feline hemoplasma strain.

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Cited by 12 publications
(5 citation statements)
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References 17 publications
(12 reference statements)
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“…The complete singular circular chromosome of M. haemocanis strain Illinois has a size of 919 992 base pairs (bp) and G + C content of 35%; these genomic features are similar to other hemoplasmas species sequenced to date [ 23 , 24 , 26 , 27 ] and within the range reported for other members of the genus Mycoplasma (Table 1 ). As described for all sequenced mycoplasmas (24 species to date), M. haemocanis also uses the opal stop codon (UGA) for tryptophan.…”
Section: Resultssupporting
confidence: 61%
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“…The complete singular circular chromosome of M. haemocanis strain Illinois has a size of 919 992 base pairs (bp) and G + C content of 35%; these genomic features are similar to other hemoplasmas species sequenced to date [ 23 , 24 , 26 , 27 ] and within the range reported for other members of the genus Mycoplasma (Table 1 ). As described for all sequenced mycoplasmas (24 species to date), M. haemocanis also uses the opal stop codon (UGA) for tryptophan.…”
Section: Resultssupporting
confidence: 61%
“…Based on the metabolic pathway predictions and specific metabolic deficiencies, a more comprehensive medium can be designed [ 33 ]. To date, only three other species of hemoplasmas have been entirely sequenced [ 23 - 27 ]. The genome features of M. haemocanis , including its small size, low G + C content and use of UGA codon to encode tryptophan, are similar to those of other hemoplasmas and are typical of members of the genus Mycoplasma .…”
Section: Discussionmentioning
confidence: 99%
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“…Interestingly, in contrast to most of the other parasites/pathogens, which are characterized by low and persistent infection dynamics, some species of haemoplasmas including MHLB (a) are persistent in all individuals and (b) are horizontally transmitted; additionally, there is (c) no indication that they may convert to disease‐causing states (as for Ca . M. haemominutum , Barker et al., ; Tasker et al., ; Willi et al., ). Future experiments should thus reveal the mechanisms of persistent haemoplasma infection.…”
Section: Discussionmentioning
confidence: 99%
“…Stenotrophomonas maltophilia RR-10, sequence accession AGRB00000000 [42] Strain HIMB30, sequence accession AGIG00000000 [43] Taylorella equigenitalis, sequence accession CP003059 [44] Vibrio campbellii DS40M4, sequence accession AGIE00000000 [45] Vibrio fischeri SR5, sequence accession AHIH00000000 [46] Yersinia enterocolitica, sequence accession AGQO00000000 [47] Phylum Tenericutes Candidatus Mycoplasma haemominutum, sequence accession HE613254 [48] Mycoplasma haemocanis strain Illinois, sequence accession CP003199 [49] Mycoplasma iowae, sequence accession AGFP00000000 [50] Mycoplasma pneumoniae Type 2a Strain 309, sequence accession AP012303 [51] …”
mentioning
confidence: 99%