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1 le as 5 ng total RNA (~equivalent to 2 x 105 bacilli).
2 growing and dividing rod-shaped cells (i.e., bacilli).
3 but contained higher levels of intracellular bacilli.
4 observed in the BaSET knock-out (BaDeltaSET) bacilli.
5 s septal peptidoglycan to separate chains of bacilli.
6 obacterial infection, where they phagocytose bacilli.
7 f flotation procedures for concentrating the bacilli.
8 molar bactericidal activity against tubercle bacilli.
9 etic genes associated with the trp operon in bacilli.
10 bial effects against vegetative B. anthracis bacilli.
11 xygen depletion and hence by non-replicating bacilli.
12 against both replicating and non-replicating bacilli.
13  in the evolutionary lineage that led to the bacilli.
14 e evolution, dynamics, and plasticity in the bacilli.
15 crophages had a heavy burden of live leprosy bacilli.
16 TagO resulted in deformed, S-layer-deficient bacilli.
17 les nicotinamide acquisition by the tubercle bacilli.
18 ents clinically useful against Gram-negative bacilli.
19 s for the long-term survival of the tubercle bacilli.
20 oth growth and oxygen consumption of treated bacilli.
21 ensitivity exhibited by members of the genus Bacilli.
22  to cavitation and the release of infectious bacilli.
23 als induce them to germinate into vegetative bacilli.
24 tive to temperature changes than that of the Bacilli.
25 hite pulp, p40(+) DC rarely colocalized with bacilli.
26 erobic and anaerobic respiratory pathways in bacilli.
27 c acid within the cell wall peptidoglycan of bacilli.
28 d CFU counts that ranged from 10(4) to 10(8) bacilli.
29  exposure to live Mycobacterium tuberculosis bacilli.
30 to the envelope of predivisional sporulating bacilli.
31 e or device) due to non-HACEK, gram-negative bacilli.
32 eration of germinating spores and vegetative bacilli.
33  to extensively drug-resistant Gram-negative bacilli.
34 ert can detect DNA from nonviable, nonintact bacilli.
35  intact or heat-lysed and mechanically lysed bacilli.
36 nes in 108 multidrug-resistant Gram-negative bacilli.
37 00 kDa-1 mum) had more free/single cocci and bacilli.
38  IL) for the identification of Gram-negative bacilli.
39  of concept for genetic exchange in tubercle bacilli.
40 arly bactericidal phase with treatment-naive bacilli.
41 at kills both replicating and nonreplicating bacilli.
42  for fluoroquinolone-resistant gram-negative bacilli.
43 entially growing and non-replicating hypoxic bacilli.
44 all aggregates containing similar numbers of bacilli.
45 orrelate with the release of viable airborne bacilli.
46 of clostridia compare with that of spores of bacilli?
47  0.05), and colistin-resistant Gram-negative bacilli (0.7 per thousand vs 1.9 per thousand; p = 0.04)
48 96) of sputum samples with a known number of bacilli (10(7) to 10(2) bacilli) could be enumerated wit
49  staphylococci, and nosocomial gram-negative bacilli (27%).
50 d primarily dominated by Clostridia (48.5%), Bacilli (27.9%), and beta-Proteobacteria (13.4%).
51                         Eighty Gram-negative bacilli (54 Enterobacteriaceae and 26 nonfermenting Gram
52 iated with multidrug-resistant gram-negative bacilli (9 vs 24 episodes; 10.8 vs 28.6 episodes/100 per
53  vs. 4%; P=0.047) with enteric gram-negative bacilli accounting for the remaining infections.
54 emonstrates that in the presence of BTZ, the bacilli accumulate DPR and fail to recycle decaprenyl ph
55 ial growth and those with positive acid fast bacilli (AFB) growth were tested to detect mycobacterium
56 putum samples, each evaluated with acid-fast bacilli (AFB) smear and mycobacterial culture using liqu
57                             Sputum acid-fast bacilli (AFB) smear microscopy has suboptimal sensitivit
58 n pending results of serial sputum acid-fast bacilli (AFB) smear microscopy is standard practice in h
59 enal necrosis, and hemorrhage, and acid-fast bacilli (AFB) were seen in the lung, liver, kidney, and
60 ohistochemistry (IHC) staining for acid-fast bacilli (AFB), and mycobacterial polymerase chain reacti
61 tal microscopic images to identify acid-fast bacilli (AFB).
62  requires specialized cultures for acid-fast bacilli (AFB; AFB cultures).
63  silica-exposed mice had many more acid fast bacilli(+) (AFB(+)) organisms than from control mice.
64 or rapid enumeration of metabolically active bacilli after phage infection.
65 rapy and rifampin was active against dormant bacilli after the establishment of hypoxia, metronidazol
66 s of peptide natural products produced by 42 bacilli and 18 pseudomonads through the generation of am
67 are active in the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all of which are predicted
68 enous challenge with vegetative B. anthracis bacilli and also in a murine pulmonary anthrax model in
69 erial infection both by directly eliminating bacilli and by interacting with macrophages and dendriti
70  of the Firmicute phylum, which includes the Bacilli and Clostridia classes, are their ability to for
71 , suggesting substantial differences between bacilli and clostridia in the engulfment and spore coat
72 to be the first step in the establishment of Bacilli and Clostridia infections, we analyzed the requi
73                     Unlike the Gram-positive Bacilli and Clostridia, A. longum spores retain their ou
74         In Bacillus subtilis, and most other bacilli and clostridia, DHDPA is oxidized to DPA by the
75 bacteria, which include important pathogenic Bacilli and Clostridia, whose ability to sporulate contr
76 nes, many of which are conserved among other bacilli and clostridia.
77 imal set(s) of sporulation-specific genes in Bacilli and Clostridia.
78 d changes occurred as drugs acted on dormant bacilli and coincided with lung pathology resolution.
79  starvation is a cidal event in the tubercle bacilli and confirms that enzymes common to the de novo
80 ic link between the respiratory state of the bacilli and DosS signaling.
81 rther advances are needed to concentrate the bacilli and eliminate PCR inhibitors in paucibacillary n
82 f BslA occurred at the poles of encapsulated bacilli and enabled the binding of vegetative forms to h
83 nificantly shorter for enteric Gram-negative bacilli and enterococci (means, 3.6 h and 2.3 h shorter,
84 to a paracrystalline layer on the surface of bacilli and form S layers.
85  3.5% of lung samples were positive for live bacilli and granulomas, respectively.
86 ons to support cell separation of vegetative bacilli and growth in infected mammalian hosts.
87 ription and translation inside the recipient bacilli and its attenuation by antibiotics.
88 drugs that enhance eradication of persistent bacilli and latent tuberculosis.
89 conjunctival secretions showed gram-negative bacilli and regular, grey non-hemolytic colonies appeari
90                         Mphi were exposed to bacilli and spores of Sterne strain 34F2 and its congeni
91 ng attachment of wall teichoic acid (WTA) in bacilli and staphylococci and capsular polysaccharides (
92  highly infectious agents, such as acid-fast bacilli and systemic fungi, were revealed.
93 is one of the mostly highly conserved in the Bacilli and the Clostridia.
94 e solely to a germination defect, since both bacilli and toxins were detected in vivo, suggesting tha
95 roteobacteria (ie, Gram-negative facultative bacilli) and relative paucity of strict anaerobic bacter
96                              Actinobacteria, Bacilli, and many Gammaproteobacteria taxa discriminated
97 is cell wall was dramatically reduced as the bacilli approached stationary phase, whereas LM, mycolic
98 smitted by the air, yet the process by which bacilli are aerosolized has received little attention.
99                        Aerobic gram-negative bacilli are frequently copathogens in infections that ar
100 as following release from lysed macrophages, bacilli are in intimate contact with these lung surfacta
101 eta-lactamase (ESBL)-producing gram-negative bacilli are increasingly reported in patients with a var
102 berculosis life cycle proposes that airborne bacilli are inhaled and phagocytosed by alveolar macroph
103 tilis PB-transporter YclNOPQ in PB-producing Bacilli are likely contributors to the pathogenicity of
104  caused by multidrug-resistant gram-negative bacilli are limited.
105 allographic analyses how the Rap proteins of bacilli are regulated by their inhibitor Phr peptide and
106 te their ancient separation, the two leprosy bacilli are remarkably conserved and still cause similar
107 latent infection, Mycobacterium tuberculosis bacilli are retained within granulomas in a low-oxygen e
108                                              Bacilli are ubiquitous low G+C environmental Gram-positi
109 yme naturally expressed/secreted by tubercle bacilli) as a marker and the design of BlaC-specific flu
110 ructural gene results in elongated chains of bacilli, as observed with a bslO mutant.
111 ere Betaproteobacteria, Sphingobacteria, and Bacilli became more abundant.
112 dose-dependent manner, and phosphate-starved bacilli became phenotypically tolerant to isoniazid.
113 in patients with less frequent Gram-negative bacilli bloodstream infections.
114 ow that it is dominated by Clostridia and/or Bacilli but also harbors Bacteroidetes.
115  to the depletion of logarithmically growing bacilli but also to the emergence of isoniazid resistanc
116 acterial effects on extracellular vegetative bacilli but do not have activity against extracellular o
117 a-lactamase, an enzyme expressed by tubercle bacilli, but not by their eukaryotic hosts, to allow rea
118 EAT antibodies promote opsonophagocytosis of bacilli by alveolar macrophages.
119 hreat Alert test strips, in detecting plague bacilli by using whole-blood samples from mice experimen
120 h rates of relapse because subpopulations of bacilli can survive despite being genetically identical
121 ses, and yield of sputum smear for acid-fast bacilli cases.
122                                Gram-negative bacilli causing infective endocarditis (IE) is rare, eve
123 iostimulation of ureolysis were significant: Bacilli class abundancy increased from 5% in the native
124 low-G+C Gram-positive bacteria (Firmicutes), Bacilli, Clostridia and Negativicutes, include numerous
125 tics for the identification of Gram-negative bacilli commonly isolated from blood cultures.
126    Infections due to resistant gram-negative bacilli continue to cause unacceptable morbidity and mor
127 th a known number of bacilli (10(7) to 10(2) bacilli) could be enumerated within 0.5 log(10).
128 roducing glucose-nonfermenting Gram-negative bacilli (CPNFs), including Pseudomonas aeruginosa and Ac
129 sistant non-glucose-fermenting Gram-negative bacilli (CR-NF) in their institution and what methods sh
130 h or virulence of Mycobacterium tuberculosis bacilli depends on homologous type VII secretion systems
131 cted with toxin-secreting Bacillus anthracis bacilli developed a rapid and marked imbalance in the en
132                                Drug-tolerant bacilli displayed marked downregulation of genes associa
133 y (DPV) response from as low as 1 CFU of Mtb bacilli DNA input material, having shown its exquisite s
134                                              Bacilli dominated the 'core' community consisting of 198
135 ial classes with Bacteroidia, Clostridia and Bacilli dominating the microbiota.
136 ning Gram-negative bacteria or Gram-positive bacilli during systemic infection.
137 hibitors could effectively target persisting bacilli during the chronic phase of tuberculosis.
138 ntensive care unit are enteric Gram-negative bacilli, enterococci, Candida species, and Pseudomonas a
139                   Mycobacterium tuberculosis bacilli exhibit cell wall alterations during in vivo gro
140       We hypothesized and proved that motile bacilli expressing a bactericide can also kill a heterol
141 ed and COGs were mostly found in Clostridia, Bacilli (Firmicutes), and in alpha and beta Proteobacter
142             Incomplete clearance of tubercle bacilli frequently results in disease relapse, presumabl
143 system of the host apart from protecting the bacilli from nitrosative stress inside the activated mac
144 -gamma-d-glutamic acid capsule that protects bacilli from phagocytic killing during infection.
145 H) assays for the detection of Gram-negative bacilli from positive blood cultures was evaluated in a
146 assessed the recovery rates of Gram-negative bacilli from stored endotracheal aspirates frozen with a
147          All eyes demonstrated gram-positive bacilli from the aqueous and B cereus was isolated, whic
148     Furthermore, NO scavengers protected the bacilli from the lethal effects of the drug.
149 h decreased in association with clearance of bacilli from the lungs.
150 utes to the escape of significant numbers of bacilli from the thoracic cavity to cause anthrax after
151 cies affiliated with the classes Clostridia, Bacilli, Gammaproteobacteria, Epsilonproteobacteria, Bac
152                                Gram-negative bacilli (GNB) bacteremia is typically transient and usua
153 tibiotics for the treatment of gram-negative bacilli (GNB) bloodstream infections (BSIs) in patients
154 s of multidrug-resistant (MDR) Gram-negative bacilli (GNB) by broth microdilution with polysorbate 80
155 ay correctly identified all 51 Gram-negative bacilli (GNB) from positive blood cultures and all 14 ca
156  to treat infections caused by gram-negative bacilli (GNB) resistant to currently available agents.
157 om blood cultures positive for Gram-negative bacilli (GNB).
158 tensively drug-resistant (XDR) Gram-negative bacilli (GNB).
159           Tissues containing M. tuberculosis bacilli had higher levels of M. tuberculosis-specific Ig
160  rate and genetic intractability of tubercle bacilli has hindered progress toward understanding tuber
161 tuberculosis drugs active against persistent bacilli has led to our interest in metallodependent clas
162 at isoniazid preclearance of M. tuberculosis bacilli has little effect on the magnitude, persistence,
163                  Bacillus subtilis and other Bacilli have long been used as biological control agents
164                                In rod-shaped bacilli, helical cables of actin-like MreB protein stret
165  cultures (BCs) that contained Gram-negative bacilli identified by Gram staining, we isolated bacteri
166 odel is presented of the growth and death of bacilli in a granuloma.
167 gh isoniazid therapy caused rapid killing of bacilli in guinea pig lungs during the first 14 days of
168                   We evaluated drug-tolerant bacilli in human sputum by comparing messenger RNA (mRNA
169         Targeting Mycobacterium tuberculosis bacilli in low-oxygen microenvironments, such as caseous
170 elated with an increase in lactate-producing bacilli in post-meconium samples (rho = -0.45; P = .004)
171 iptional patterns suggest that drug-tolerant bacilli in sputum are in a slow-growing, metabolically a
172 in showed many more neutrophils and ingested bacilli in the athymic mice.
173 x lethal toxin was required for outgrowth of bacilli in the draining lymph nodes and subsequent progr
174 ty and transmission dynamics of the tubercle bacilli in the Republic of Korea.
175 us and vitreous samples showed gram-negative bacilli in the smears of 8 of 11 eyes, and cultures grew
176 bial effects against B. anthracis spores and bacilli including marked reductions in spore and bacillu
177  isoniazid stress signature in drug-tolerant bacilli indicates that physiological state influences dr
178 combined with their ability to kill tubercle bacilli, indicates great potential for translational dev
179  that specificity of endolysins for specific bacilli is achieved by selective binding to a uniquely g
180 bapenemase (KPC) production in Gram-negative bacilli is an increasing problem worldwide.
181 culminates in the transmission of infectious bacilli is determined locally at the level of the granul
182                      Entry to sporulation in bacilli is governed by a histidine kinase phosphorelay,
183 iscovered that a subpopulation of planktonic bacilli is propelled by flagella to tunnel deep within a
184 orrodens, or Kingella species) gram-negative bacilli is rare, is poorly characterized, and is commonl
185 embers of the animal lineage of the tubercle bacilli is very rare.
186  a group of fastidious Gram-negative aerobic bacilli isolated mostly from blood samples from patients
187  percentage of lipid body-positive acid-fast bacilli (%LB + AFB) on sputum smears.
188 e is representative of CsoRs from pathogenic bacilli Listeria monocytogenes and Bacillus anthracis.
189                                    Some soil Bacilli living in association with plant roots can prote
190 condary cell wall polysaccharides of various bacilli may have both common and variable structural fea
191  to M. bovis infection and that the M. bovis bacilli may survive within the cysts of four of these sp
192 ation with multidrug-resistant Gram-negative bacilli (MDR GNB) and compared the results with those of
193       Cultures of valve tissue for acid-fast bacilli might be considered in some cases of apparently
194 bacterial decline during the same 3 days and bacilli ml(-1) sputum at day 0 (linear regression, P = 0
195 f microenvironments to which M. tuberculosis bacilli must adapt.
196                                     Airborne bacilli must be capable of surviving in the external env
197                                       Viable bacilli must then be released as an aerosol via the resp
198 ows and sheep, is caused by slow replicating bacilli Mycobacterium avium subspecies paratuberculosis
199 dentification of nonfermenting Gram-negative bacilli (NFB) is crucial for patient management.
200 dentification of nonfermenting gram-negative bacilli (NFGNB) by a blinded comparison to conventional
201  (n = 150) and nonfermentative gram-negative bacilli (NFGNB; 45 clinical isolates and 8 challenge iso
202 ng in macrophages that neither sterilize the bacilli nor allow them to cause disease.
203 t cells, human CD68(+) macrophages, and high bacilli numbers surrounded by a layer of CD3(+) T cells
204 teriaceae and 26 nonfermenting Gram-negative bacilli) obtained from multiple institutions in the Unit
205 of chromosomal DNA transfer between tubercle bacilli of the early-branching Mycobacterium canettii cl
206 age particles associated with the surface of bacilli of the Sterne strain but not with the surfaces o
207 bapenemase detection among 271 Gram-negative bacilli (of which 131 were carbapenemase producers) usin
208 ut sputum smears were negative for acid-fast bacilli on 3 consecutive days) and 22,716 cases of inact
209  B. anthracis Ames contained high numbers of bacilli, only few vegetative forms could be recovered fr
210 cuum manifold and is designed to concentrate bacilli onto a filter that can be examined microscopical
211  of B. anthracis Sterne spores or vegetative bacilli onto intact or abraded mouse flank skin, followe
212 the MTBDRplus assay after positive acid-fast bacilli or culture.
213 s for identification of common gram-negative bacilli (P > 0.05).
214 ation of infrequently isolated gram-negative bacilli (P < 0.0001).
215 to multidrug-resistant aerobic Gram-negative bacilli (p = 0.008).
216                    The evolution of tubercle bacilli parallels a route from environmental Mycobacteri
217 ulosis (TB), some Mycobacterium tuberculosis bacilli persist in the presence of an active immunity an
218       Unlike phagosomes containing wild-type bacilli, phagosomes containing the DeltacpsA mutant recr
219 rior to infection with 10(5) M. tuberculosis bacilli prevented weight loss and enhanced pulmonary myc
220 ith active tuberculosis, indicating that the bacilli produce pili or pili-associated antigen during h
221     The non-glucose-fermenting Gram-negative bacilli Pseudomonas aeruginosa and Acinetobacter baumann
222  latent tuberculosis (TB) infection, dormant bacilli putatively reside within the hypoxic environment
223 ed at oxygen levels between 0.5 and 10%, the bacilli remained viable throughout the 4 d of culture.
224       Despite reduced phagocytosis, ingested bacilli replicated at a fast rate following serum opsoni
225 ignificant isolates of aerobic Gram-positive bacilli representing 20 genera and 38 species.
226           Here we asked whether encapsulated bacilli require BslA for anthrax pathogenesis in guinea
227 n-replicating persistence indicated that the bacilli require electron transport chain components and
228 itical lesion site where persisting tubercle bacilli reside.
229 ion of antibiotics into granulomas where the bacilli reside.
230 ue caused millions of deaths, and the plague bacilli's potential for weaponization sustains an ongoin
231                    Although present all over bacilli, Sap S-layer patches are not observed at septa.
232    In lethal systemic anthrax, proliferating bacilli secrete large quantities of the toxins lethal fa
233 e patterns along the long axis of rod-shaped bacilli, similar to the localization of lipid II.
234 d increase in the highest grade of acid-fast bacilli smear (AFS).
235  scores (P = 0.016), higher sputum acid-fast bacilli smear microscopy grades (P = 0.007), lower days
236                   Frequency of CSF acid-fast-bacilli smear positivity was 8.9% (95% CI 5.0-15.4), and
237 red and fifty-seven direct patient acid-fast bacilli smear-positive specimens resistant to isoniazid,
238 infection than the standard sputum acid-fast bacilli smear.
239 rcent (680/848) of patients having acid-fast-bacilli-smear-positive specimens had MTD performed; MTD
240  testing of skin-biopsy specimens, acid-fast bacilli smears, and microbial cultures and antimicrobial
241                          Unlike the case for Bacilli species, d-alanine had no effect on C. sordellii
242             We show that infection with live bacilli specifically alters the expression of host genes
243 -37 concentrations correlated with acid fast bacilli sputum smear positivity and weight gt 10% below
244                                Gram-negative bacilli, Staphylococcus aureus, Chlamydia, Mycoplasma, a
245 ely resistant and panresistant Gram-negative bacilli, such as Acinetobacter baumannii, requires consi
246 nd drug-specific effect on the proportion of bacilli surviving antibiotic killing.
247  C10OOc12O was able to enhance gram-negative bacilli susceptibility to antibacterial components of th
248 f virulence after intravenous challenge with bacilli than deletion of lethal toxin or edema toxin alo
249 tests based on products secreted by tubercle bacilli that are strictly associated with viability, we
250          Rothia spp. are Gram-positive cocco-bacilli that cause a wide range of serious infections, e
251 al enzyme probe to detect and image tubercle bacilli that demonstrates REF is likely to be useful for
252 ition of BslO onto the surface of sap mutant bacilli that extends beyond chain septa.
253 its natural environment, C. elegans feeds on Bacilli that possess functional NOS.
254   Gordonia species are aerobic Gram-positive bacilli that rarely cause human infections, often in the
255 play a significant role in the generation of bacilli that survive in the face of multidrug therapy or
256 enger RNA (mRNA) expression of drug-tolerant bacilli that survive the early bactericidal phase with t
257 ecrotizing granuloma (negative for acid-fast bacilli) that grew Mycobacterium kansasii on culture.
258 herefore be useful in fighting gram-negative bacilli threats through sensitization to endogenous and/
259 s, indicating that recognition of vegetative bacilli through Nod1/Nod2 is significant.
260  phase but resulted in substantially shorter bacilli throughout the growth cycle.
261 nd granulomatous lesions containing tubercle bacilli throughout the meninges, all of which were absen
262 ing bacteria with ubiquitin, and delivery of bacilli to autophagosomes requires the ubiquitin-autopha
263 terilization, is based on the ability of the bacilli to be reactivated after immune suppression.
264         We modified microscopy for acid-fast bacilli to diagnose tuberculosis (TB) using small membra
265 vide additional surface molecules that allow bacilli to engage cells or tissues of specific hosts dur
266  of mycobacterial proteins from phagocytosed bacilli to exosomes was dependent on protein ubiquitinat
267 graphed succession of bacterial classes from Bacilli to Gammaproteobacteria to Clostridia, interrupte
268 ics, we attempted to sensitize gram-negative bacilli to innate antibacterial protagonists.
269             After intravenous challenge with bacilli to model the systemic phase of infection, lethal
270  appropriate cellular response and helps the bacilli to overcome the onslaught of host defence mechan
271 nergy and biosynthetic precursors in growing bacilli to pathways for storage compound synthesis durin
272 f anthrax-like disease and the resistance of bacilli to phagocytosis.
273  nutrient starvation, thus enabling tubercle bacilli to restrict growth and shut down metabolism in a
274  spectrum that runs from elimination of live bacilli to subclinical disease: hence, it might be unhel
275  mice with monocytes incapable of delivering bacilli to the autophagy pathway are extremely susceptib
276  Phoenix for identification of gram-negative bacilli to the genus (P < 0.0001) and species (P = 0.000
277     Finally, deletion of bas0520 resulted in bacilli unable to grow efficiently on heme or hemoglobin
278 that the viability and purity of the leprosy bacilli used for in vitro studies determines the extent
279 ry specimens that are negative for acid-fast bacilli using smear microscopy.
280 ) system for identification of gram-negative bacilli, using biochemical testing and/or genetic sequen
281 mma-DPGA) capsule released from B. anthracis bacilli was associated with LT in animal blood in variab
282 fected with either wild-type or ESX-1 mutant bacilli, we found that host genes controlled by ESX-1 in
283                     With a fixed inoculum of bacilli, we were able to reproducibly generate cavities
284 , only live M. avium subsp. paratuberculosis bacilli were able to prevent phagosome maturation and re
285 3-IS levels, whereas members of the class of Bacilli were associated with low 3-IS levels.
286 P10, in the presence and absence of RIF, and bacilli were enumerated using FACS.
287 0 Bactec bottles demonstrating Gram-negative bacilli were prospectively enrolled for this study.
288 and infection by nonfermenting gram-negative bacilli were significantly associated with hospital mort
289 eus, S. mitis, Corynebacterium accolens, and bacilli were significantly more abundant in infants with
290 ided with rapid killing of actively dividing bacilli, whereas slower delayed changes occurred as drug
291 ith the extremely long chain lengths of csaB bacilli, which are incapable of binding proteins with SL
292 ere found to be classic rod-shaped acid-fast bacilli, while in the stationary phase M. smegmatis lost
293 erated cavitary CFU counts of 10(6) to 10(9) bacilli, while non-M. bovis species and BCG yielded CFU
294 ple different gene clusters endow pathogenic bacilli with capsular material, provide for escape from
295 -layer-associated protein BslA, which endows bacilli with invasive attributes for mammalian hosts.
296  We hypothesized that preclearance of latent bacilli with IPT modulates BCG immunogenicity following
297 ivity by human NK cells against B. anthracis bacilli within infected autologous monocytes.
298 n response to the changing physiology of the bacilli within its host.
299 etative outgrowth and killing the developing bacilli within the confines of the exosporium.
300          Xpert detected nonviable, nonintact bacilli without a change in CTvs controls.
301 ectively dispersing chains of bslO-deficient bacilli without lysis and localizing to the septa of veg

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