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1 cells and in a mouse model of staphylococcal mastitis.
2 3.3, 95% CI: 1.92, 5.62) strongly predicted mastitis.
3 uarters suffering recurrent cases of E. coli mastitis.
4 (CoNS) from bovine clinical and subclinical mastitis.
5 subspecies zooepidemicus, a cause of bovine mastitis.
6 f early inflammatory responses during bovine mastitis.
7 as up-regulated on leukocytes from cows with mastitis.
8 were studied during Escherichia coli-induced mastitis.
9 7, a serum-resistant isolate from a cow with mastitis.
10 ent approach to treat lactational infectious mastitis.
11 the development of chronic S. aureus-related mastitis.
12 the dairy industry are used to treat bovine mastitis.
13 ays relevant to bovine S. aureus subclinical mastitis.
14 hanistic studies on susceptibility of bovine mastitis.
15 lead to the development of vaccines against mastitis.
16 ysbiosis of the milk microbiome that permits mastitis.
17 m dairy cattle with transient and persistent mastitis.
18 ctiae, one of the causative agents of bovine mastitis.
19 ntributing to higher milk viral loads during mastitis.
20 ient previously diagnosed with granulomatous mastitis.
21 ads in breast milk were not increased during mastitis.
22 ical processes that occur during LPS-induced mastitis.
23 ontribute to milk composition changes during mastitis.
24 hanisms affected in cows more susceptible to mastitis.
27 -32 (IL-32) in Staphylococcus aureus-induced mastitis, an inflammation of the mammary gland, is uncle
30 ith the progression of S. aureus subclinical mastitis and could be used as powerful biomarkers for th
31 ein, we develop a murine model of autoimmune mastitis and provide a detailed characterization of its
34 understanding of the epidemiology of E. coli mastitis and suggest that pathogen adaptation and host s
35 ghest homology with a GBS strain causing cow mastitis and that the 1992 ST-1 strain differed from ser
37 associated with symptomatic and asymptomatic mastitis and with the quantity of HIV-1 RNA and DNA in m
38 have been identified as causative agents in mastitis, and are traditionally diagnosed by bacterial c
39 ens but have so far not been associated with mastitis, and DNA of bacteria that are currently not kno
40 te immune responses, reduces the severity of mastitis, and facilitates clearance and neutralization o
41 Escherichia coli strains that caused bovine mastitis, and have since been implicated in many physiol
42 ing genital ulcer disease, chorioamnionitis, mastitis, and malnutrition in HIV-infected women, and of
46 notable differences in the genomes of bovine mastitis-associated and human clones of S. aureus and pr
47 omparative genomic analysis between a bovine mastitis-associated clone, RF122, and the recently seque
49 f 9.5% reported provider-diagnosed lactation mastitis at least once during the 12-week period, with 6
50 ss-sectional study, laboratory indicators of mastitis (breast milk sodium [Na(+)] concentration, sodi
51 Staphylococcus aureus commonly causes bovine mastitis, but bovine strains, unlike human isolates of S
52 e findings indicate that 38% of all clinical mastitis cases and 63% of the PTEs attributed to S. uber
54 s sequences were the third most prevalent in mastitis cases diagnosed as Staphylococcus aureus by cul
55 were the second most prevalent sequences in mastitis cases diagnosed as Streptococcus dysgalactiae b
56 were the second most prevalent sequences in mastitis cases diagnosed as Trueperella pyogenes by cult
58 olates of Streptococcus uberis from clinical mastitis cases in a study of 52 commercial dairy herds o
59 Forty-one percent of all clinical E. coli mastitis cases occurred in just 2.2% of the population.
61 acter, and Staphylococcus, often involved in mastitis cases, were the most abundant genera across tre
68 samples from women with laboratory-diagnosed mastitis (defined as elevated BM Na(+) levels) were 5.4-
70 fied DNA of bacteria that are known to cause mastitis, DNA of bacteria that are known pathogens but h
74 I: 1.37, 8.54), and (for women with no prior mastitis history) using a manual breast pump (OR = 3.3,
75 Globally, 44 of 108 women (41%) developed mastitis; however, the percentage of women with mastitis
87 titis; however, the percentage of women with mastitis in the probiotic group (25% [n = 14]) was signi
88 y important in the epidemiology of S. uberis mastitis in the United Kingdom, with cow-to-cow transmis
91 until they stopped breastfeeding to describe mastitis incidence, mastitis treatment, and any associat
92 ved in the host defense of the udder against mastitis infection and that selective recruitment of the
99 cell line (MAC-T) by a Staphylococcus aureus mastitis isolate to study the potential role of intracel
104 ed breast milk sodium levels consistent with mastitis occurred in 16.4% of HIV-1-infected women and w
106 itis treatment, and any associations between mastitis occurrence and hypothesized host characteristic
108 ipple thrush) in the same 3-week interval as mastitis (OR = 3.4, 95% CI: 1.37, 8.54), and (for women
109 cracks and nipple sores in the same week as mastitis (OR = 3.4, 95% CI: 2.04, 5.51), using an antifu
111 clinical presentations in cattle, including mastitis, otitis, arthritis, and reproductive disorders.
114 e involved in the response of the udder to a mastitis pathogen and if the type of mastitis pathogen i
115 er to a mastitis pathogen and if the type of mastitis pathogen influenced the subset composition of t
117 taphylococcus aureus is the major contagious mastitis pathogen, accounting for approximately 15-30% o
119 reast-feeding (OR, 1.7; 95% CI, 1.0-2.9) and mastitis (relative risk [RR], 3.9; 95% CI, 1.2-12.7) wer
123 ted with increased transmission overall, and mastitis (RR, 21.8; 95% CI, 2.3-211.0) and breast absces
124 mphocytes in cows with S. aureus subclinical mastitis (SA group) and healthy controls (CK) were gener
126 ide isolated from the cell envelop of bovine mastitis Streptococcus dysgalactiae 2023 is reported for
127 The chronic nature of bovine staphylococcal mastitis suggests that some products or components of S.
132 85.7% of cases of recurrent quarter E. coli mastitis, the same genotype was implicated as the cause
133 althy cows and cows with naturally occurring mastitis to determine if distinct alphabeta and gammadel
134 reastfeeding to describe mastitis incidence, mastitis treatment, and any associations between mastiti
136 numbers observed in cows with streptococcal mastitis was due to a parallel increase in both CD4(+) a
138 ollected from cows in August, 1998, although mastitis was evident among cows on the suspected farm.
139 requency in the same week or the week before mastitis was included in the model (for the same week: 7
143 served in milk from cows with staphylococcal mastitis was primarily due to increased numbers of CD4(+
144 the acute host response to Escherichia coli mastitis, we analyzed gene expression patterns of approx
145 experiment modeling phage therapy for bovine mastitis, we observed pathogenicity island transfer betw
146 h confirmed staphylococcal and streptococcal mastitis were characterized by increased numbers of gamm
147 olved in recurrent cases of clinical E. coli mastitis were compared by DNA fingerprinting with entero
148 m cows with staphylococcal and streptococcal mastitis were due to a selective recruitment of a distin
149 y virus (HIV) type 1 load in breast milk and mastitis were examined as risk factors for vertical tran
150 very, HIV-1 load and sodium (an indicator of mastitis) were measured in breast milk from 334 HIV-1-in
151 t in a logistic regression model, history of mastitis with a previous child (odds ratio (OR) = 4.0, 9
152 f the nipple, previous treatment for Candida mastitis with oral or topical antifungals was ineffectiv
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