HOST METABOLITES THAT PHENOTYPICALLY INCREASE THE RESISTANCE OF HAEMOPHILUS-INFLUENZAE TYPE-B TO CLEARANCE MECHANISMS

被引:20
作者
KURATANA, M
ANDERSON, P
机构
[1] UNIV ROCHESTER,MED CTR,DEPT MICROBIOL,POB 690,ROCHESTER,NY 14642
[2] UNIV ROCHESTER,MED CTR,DEPT PEDIAT,ROCHESTER,NY 14642
关键词
D O I
10.1093/infdis/163.5.1073
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unidentified low-molecular-weight factor(s) in serum or nasopharyngeal secretions were known to phenotypically increase the resistance of Haemophilus influenzae type b (Hib) to bactericidal and opsonic antibodies, and resistance was attributed to two hypothetical mechanisms. Serum components generating resistance were studied. Mechanism 1, present in some Hib strains and their capsule-deficient mutants and accompanied by apparent increases in lipopolysaccharide content, was reproduced with a mixture of glucose, lactate, urea, and bicarbonate. Mechanism 2, present only in capsulated Hib and accompanied by increased capsulation, was reproduced with a mixture of Ca++ and lactate. Hib incubated with these compounds in buffer or grown in serum filtrate was resistant, but Hib grown in conventional media containing the metabolites was not. The resistant phenotype, which resembles Hib in vivo, may depend on nutrient balance as well as the specific factors. Lactate apparently is an important energy source for Hib.
引用
收藏
页码:1073 / 1079
页数:7
相关论文
共 25 条
[1]  
ANDERSON P, 1978, J IMMUNOL, V120, P866
[2]   PHENOTYPIC AND GENETIC-VARIATION IN THE SUSCEPTIBILITY OF HEMOPHILUS-INFLUENZAE TYPE-B TO ANTIBODIES TO SOMATIC ANTIGENS [J].
ANDERSON, P ;
FLESHER, A ;
SHAW, S ;
HARDING, AL ;
SMITH, DH .
JOURNAL OF CLINICAL INVESTIGATION, 1980, 65 (04) :885-891
[3]   PHAGOCYTE-DERIVED LACTATE STIMULATES OXYGEN-CONSUMPTION BY NEISSERIA-GONORRHOEAE - AN UNRECOGNIZED ASPECT OF THE OXYGEN-METABOLISM OF PHAGOCYTOSIS [J].
BRITIGAN, BE ;
KLAPPER, D ;
SVENDSEN, T ;
COHEN, MS .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (02) :318-324
[4]  
Davis BD, 1979, MICROBIOLOGY
[5]   CONSERVATION OF EPITOPES IN THE OLIGOSACCHARIDE PORTION OF THE LIPOOLIGOSACCHARIDE OF HAEMOPHILUS-INFLUENZAE TYPE-B [J].
GULIG, PA ;
PATRICK, CC ;
HERMANSTORFER, L ;
MCCRACKEN, GH ;
HANSEN, EJ .
INFECTION AND IMMUNITY, 1987, 55 (03) :513-520
[6]   IDENTIFICATION OF IMMUNOGENIC OUTER-MEMBRANE PROTEINS OF HEMOPHILUS-INFLUENZAE TYPE-B IN THE INFANT RAT MODEL SYSTEM [J].
HANSEN, EJ ;
FRISCH, CF ;
MCDADE, RL ;
JOHNSTON, KH .
INFECTION AND IMMUNITY, 1981, 32 (03) :1084-1092
[7]   DEFINED MEDIUM FOR GROWTH OF HAEMOPHILUS-INFLUENZAE [J].
HERRIOTT, RM ;
MEYER, EY ;
VOGT, M ;
MODAN, M .
JOURNAL OF BACTERIOLOGY, 1970, 101 (02) :513-&
[8]   A CHEMICALLY DEFINED MEDIUM INDUCES RESISTANCE TO LIPOPOLYSACCHARIDE ANTIBODY IN HAEMOPHILUS-INFLUENZAE TYPE-B [J].
INZANA, TJ .
MICROBIAL PATHOGENESIS, 1986, 1 (05) :483-489
[9]   SERUM FACTOR DEPENDENT RESISTANCE OF HEMOPHILUS-INFLUENZAE TYPE-B TO ANTIBODY TO LIPOPOLYSACCHARIDE [J].
INZANA, TJ ;
ANDERSON, P .
JOURNAL OF INFECTIOUS DISEASES, 1985, 151 (05) :869-877
[10]   ELECTROPHORETIC HETEROGENEITY AND INTERSTRAIN VARIATION OF THE LIPOPOLYSACCHARIDE OF HEMOPHILUS-INFLUENZAE [J].
INZANA, TJ .
JOURNAL OF INFECTIOUS DISEASES, 1983, 148 (03) :492-499