Pleasecitethisarticleinpressas:Carvalho-CastroGA,etal.MolecularepidemiologyofStreptococcus agalactiaeisolatedfrommastitisinBrazilianIntroduction Escherichia coli, Klebsiella pneumoniae,
Trang 1h tt p : / / w w w b j m i c r o b i o l c o m b r /
Rafael O Moreirab, Glaucia F Miana, Ingrid A Pradoa, Antônio Chalfun-Juniorb,
Geraldo M Costaa, ∗
aFederal University of Lavras, Laboratory of Bacteriology, Lavras, Brazil
bFederal University of Lavras, Central Laboratory of Molecular Biology, Lavras, Brazil
a r t i c l e i n f o
Article history:
Keywords:
a b s t r a c t
Streptococcus agalactiaeisoneofthemostcommonpathogensleadingtomastitisindairy
hylB, fbsA, fbsB,PI-1,PI-2a,andPI-2b,whichareassociatedwithadhesion,invasion,tissue
licenses/by-nc-nd/4.0/)
∗ Corresponding author at: Laboratory of Bacteriology, Department of Veterinary Medicine, Federal University of Lavras, Lavras,
http://dx.doi.org/10.1016/j.bjm.2017.02.004
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Introduction
Escherichia coli, Klebsiella pneumoniae, Streptococcus agalactiae,
Streptococcus uberis,andStaphylococcus aureus.2,4,5S agalactiae,
herds
Materials and methods
Bacterial strains
identi-fiedasS agalactiaephenotypicallybythecatalasetest,CAMP
dysgalactiaestrain(ATCC27957)wasusedasthenegative
assays
Specific PCR, molecular capsular typing and sequencing
S agalactiae classificationbyusingS agalactiae-specificPCR
Multilocus sequence typing and clonal group assignment
Trang 3pheS, phenylalanyl transfer RNA synthetase; atr, amino
S agalactiae MLST database The eBURST V3 programme
(http://eburst.mlst.net)20 was then used to identify clonal
Genetic relationship of S agalactiae isolated from different
hosts in Brazil
Detection of virulence genes
Statistical and data analysis
Results
Table 1 presents all of the data generated during our
(Table1 InST-103,ST-146,andST-314,thefrequencydropped
study
S agalactiaestrainsinthisstudywereclusteredintotwomain
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Table 1 – Characteristics and frequency of 59 Group BStreptococcus(GBS) isolates listed according to capsular type,
sequence type, and clonal complex.
STa Allelicprofile No.ofisolates
inST(%)
Capsulartype(no.ofisolates) Mastitistype(no.ofisolates) Stateoforiginc
(no.ofisolates)
CCb
61 13,1,1,13,1,1,1 11(18.33%) III(9),Ia(1),NT(1) Clinical(3)/Subclinical(8) MG(7),SP(3),PE(1) 61
67 13,1,1,13,1,1,5 21(35.59%) Ia(1),II(12),III(3),IV(3),NT(2) Clinical(5)/Subclinical(16) MG(7),PE(6),SP(8) 67
91 25,1,1,13,15,1 9(15.25%) III(8),IV(1) Clinical(4)/Subclinical(5) MG(8),PE(1) 91
570 16,1,1,2,1,1,5 7(11.8%) Ib(5),IV(1),NT(1) Subclinical(7) MG(1),PR(6) 67
a ST:sequencetype
b CC:clonalcomplex
c States:MG,MinasGerais;SP,SãoPaulo;PE,Pernambuco;PR,Parana
Discussion
tobeS agalactiae.Thisresultwasnotcompletelyunexpected
CC67 (ST–67; ST–570)
CC314 (ST–226; ST–314)
CC64 (ST–61)
CC17 (ST–146)
CC103 (ST–103)
Singleton 91
Trang 5ST–91
ST–67 ST–570 ST–256 ST–26 ST–2 ST–103 ST–226 ST–314 ST–553 ST–260 ST–552
CC 552
CC 314 CC103 CC19 CC26 CC67 CC17
CC64 ST–91
ST–146
66 70 93
47
100
100 100
71 90
inStreptococcusbacteria.29,40 Anotherpossiblecauseforthis
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pres-sure/diversity
hypothesis
ofS agalactiaewereevaluated,CC17andCC61wereclustered
sev-eralStreptococcusspecieshaveretaineddistinctcharacteristics
inS agalactiaestrainsisolatedfrom bovines.Although
Trang 7S agalactiaeisolatedfromBrazilianbovines,whichisessential
pathogen
Funding
fellowship
Conflict of interest
Appendix A Supplementary data
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