Chemotaxigenesis by encapsulated Staphylococcus aureus M

D. J. Schmeling; P. K. Peterson; I. M. Barr; Y. Kim; P. G. Quie

doi:10.1128/iai.27.2.700-703.1980

Chemotaxigenesis by encapsulated Staphylococcus aureus M

D. J. Schmeling
, P. K. Peterson
, I. M. Barr
, Y. Kim
, P. G. Quie

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

Although encapsulated Staphylococcus aureus M is not opsonized by normal human serum, as a chemotaxigen this organism behaved similarly to an unencapsulated variant strain. For optimal chemotaxigenesis, an intact classical complement pathway was required, and C5a appeared to be the major chemotaxin.

Original language	English (US)
Pages (from-to)	700-703
Number of pages	4
Journal	Infection and immunity
Volume	27
Issue number	2
DOIs	https://doi.org/10.1128/iai.27.2.700-703.1980
State	Published - 1980

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@article{f852819d9cc445059465c0fb782a7fab,

title = "Chemotaxigenesis by encapsulated Staphylococcus aureus M",

abstract = "Although encapsulated Staphylococcus aureus M is not opsonized by normal human serum, as a chemotaxigen this organism behaved similarly to an unencapsulated variant strain. For optimal chemotaxigenesis, an intact classical complement pathway was required, and C5a appeared to be the major chemotaxin.",

author = "Schmeling, \{D. J.\} and Peterson, \{P. K.\} and Barr, \{I. M.\} and Y. Kim and Quie, \{P. G.\}",

year = "1980",

doi = "10.1128/iai.27.2.700-703.1980",

language = "English (US)",

volume = "27",

pages = "700--703",

journal = "Infection and immunity",

issn = "0019-9567",

publisher = "American Society for Microbiology",

number = "2",

}

TY - JOUR

T1 - Chemotaxigenesis by encapsulated Staphylococcus aureus M

AU - Schmeling, D. J.

AU - Peterson, P. K.

AU - Barr, I. M.

AU - Kim, Y.

AU - Quie, P. G.

PY - 1980

Y1 - 1980

N2 - Although encapsulated Staphylococcus aureus M is not opsonized by normal human serum, as a chemotaxigen this organism behaved similarly to an unencapsulated variant strain. For optimal chemotaxigenesis, an intact classical complement pathway was required, and C5a appeared to be the major chemotaxin.

AB - Although encapsulated Staphylococcus aureus M is not opsonized by normal human serum, as a chemotaxigen this organism behaved similarly to an unencapsulated variant strain. For optimal chemotaxigenesis, an intact classical complement pathway was required, and C5a appeared to be the major chemotaxin.

UR - https://www.scopus.com/pages/publications/0018841246

UR - https://www.scopus.com/pages/publications/0018841246#tab=citedBy

U2 - 10.1128/iai.27.2.700-703.1980

DO - 10.1128/iai.27.2.700-703.1980

M3 - Article

C2 - 7380548

AN - SCOPUS:0018841246

SN - 0019-9567

VL - 27

SP - 700

EP - 703

JO - Infection and immunity

JF - Infection and immunity

IS - 2

ER -

Chemotaxigenesis by encapsulated Staphylococcus aureus M

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