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. 2016 May 10;7(3):e00281-16. doi: 10.1128/mBio.00281-16

TABLE 2 .

Assessment of Mycobacterium mungi infection in banded mongooses

Sample type (yr[s] of sample collection) Results for M. mungi detection bya:
PCRb
Histopathology
% positive No. of samples tested % of positive samples in agreement with necropsy result (no. positive by necropsy) % positive No. of samples tested
Anal glands (2009–2015) 33 18 100 c
Anal gland secretions (2009–2015) 39 44 100 (5)
Oral swabs (2009–2015) 53 19 100 (3)
Nasal swabs (2009–2015) 50 4 100 (1)
Nasal rinses (2015) 60 5 Status unknown
Urine (2011–2015) 22 23 60 NAd
Nasal planum (2000–2015) 29 52 69 35 34
Skin lesions (2003–2015) 100 7 100 (5) 56 9
Scrotum (2015) 100 2 100
Testicular lesions (2000–2008) 50 12
Lung (all disseminated disease) (2000–2012) 67 33
Bladder (2009–2015) 43 23 70 0 12
Kidney (2000–2012) 24 34
Feces (2013–2014) 0 113 NA
Other species feces (see text) (2013) 0 121 NA
Human feces in the environment (2012–2013) 0 12 NA
Soil from infected mongoose home ranges (2011 and 2014) 0 172 NA
a

The prevalence of positive tissue samples is presented by assessment type and, of those positive, the percentage that came from individuals determined to be positive for M. mungi infection at necropsy.

b

In PCR, samples were considered positive if primer sets for RD1BCG, RD1mic, RD1seal, and RD1mon amplified a PCR fragment of the expected size.

c

—, samples were not evaluated using the indicated diagnostic technique.

d

NA, Technique not used with this sample type.