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. 2019 Dec 20;6(1):e000303. doi: 10.1099/mgen.0.000303

Table 1.

hiHh isolates used in this study

Isolate

Anatomical site

Country of origin

Year of isolation

Haemin (X-factor) dependence*

NAD (V-factor) dependence*

Haemin biosynthesis pathway†

Genome reference

60819_B_Hi1

BAL

Australia

2010

+

C5, PP-dependent,

O2-independent

[18]

60824_B_Hi4

BAL

Australia

2010

+

C5, PP-dependent,

O2-independent

[18]

60971_B_Hi3

BAL

Australia

2012

+

C5, PP-dependent,

O2-independent

[18]

60982_B_Hi1

BAL

Australia

2012

+

C5, PP-dependent,

O2-independent

[18]

65117_B_Hi3

BAL

Australia

2011

+

C5, PP-dependent,

O2-independent

[18]

65151_B_Hi4

BAL

Australia

2011

+

C5, PP-dependent,

O2-independent

[18]

839_HINF

BAL

USA

2013

Unknown

Unknown

C5, PP-dependent,

O2-independent

[24]

CCUG 11096

Pleural fluid

Sweden

1981

+

C5, PP-dependent,

O2-independent

[3]

CCUG 15949

Eye

Sweden

1984

+

C5, PP-dependent,

O2-independent

[3]

CCUG 30218

Cerebrospinal fluid

Sweden

1992

+

C5, PP-dependent,

O2-independent

[3]

CCUG 31732

Ascitic fluid

Sweden

1993

+

C5, PP-dependent,

O2-independent

[3]

CCUG 66565

Sputum

Sweden

2014

Unknown

Unknown

C5, PP-dependent,

O2-independent

This study

F0629

Oral cavity

USA

2015

Unknown

Unknown

C5, PP-dependent,

O2-independent

This study

PN24

Urine

Denmark

2004

+

C5, PP-dependent,

O2-independent

[3]

BAL, Bronchoalveolar lavage.

*, Recorded phenotype.

†, Aminolevulinic acid biosynthesis occurs using the C5 pathway [63]; coproporphyrinogen III conversion to protohaem is protoporphyrin-dependent, and occurs in an oxygen-independent manner [63].