CA1083480A - Identification of neisseria gonorrhoeae using antibodies from lps antigen - Google Patents

Abstract

ABSTRACT OF THE DISCLOSURE

A reagent and test for the identification of the bacterium Neisseria gonorrhoeae. Lipopolysaccharide anti-gen, found to be common to N. gonorrhoeae strains, is used to inoculate fowl, and serum from the fowl recovered con-taining antibodies causing agglutination of cells of all N. gonorrhoeae strains. The identification test comprises adding the recovered antibody reagent to a suspension of bacterial cells, the occurrence of cell agglutination being a positive test for N. gonorrhoeae.

Description

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,~ , ' Field of the Invention A specific reagent and test for the identification of bacterial cells of Neisseria gonorrhoeae is described.
A common gonococcal antigen (lipopolysaccharide) has been found and used to prepare antibodies by inoculating fowl and recovering antiserum from the fowl. The resulting antibodies have been found to be capable of causing agglu-tination of cells of any N. gonorrhoeae, this agglutination .
being made the basis of a rapid identification test.
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Description of the Prior Art .
The increased incidence of bacterial disease -such as gonorrhea, which has now reached epidemic propor-tions, has focused on the need for rapid diagnostic tech-niques, in order to follow up contacts as quickly as pos-sible. Presently, tests for the identification of Neisseria gonorrhoeae obtained from clinical specimens are beset with difficulties. Sugar fermentations frequently produce un-satisfactory growth patterns, require media of high quality and are time-consuming. A slide co-agglutination method has been described, using Protein-A containing staphylo-cocci absorbed to the Fc portion of anti-gonococcal IgG
(Danielsson, D., and Kronvall, G. Appl. Microbiol. 27:368-374). However, this method requires absorption of the gono-coccal whole-cell antiserum with Neisseria meningitidis, .
and Pseudomonas aeruginosa or Morexella to render the rea-gent specific for N. gonorrhoeae. In addition, the co-. . ~ .
agglutination test when used for the identification of N.

gonorrhoeae in purity cultures grown on serum-containing medium was found to be inadequate, since 50~ of the gono-coccal strains testecl gave pseudo-coagcJlutinations with the sta~hylococcal reagent ~Menck. H. Acta path. mlcrobiol.
scand. ~ect. s 84:139-144. 1976). A radioimmunoassay has . :

8348~) been developed for detecting antibodies to _. gonorrhoeae in human serum (U.S. Patent 3,974,269~. This test which requires human blood samples and radioisotope measuring techniques is used to detect circulating antibody to _.
gonorrhoeae but does not constitute a test for the actual identification of the causative microorganism, N. gonorrhoeae.
The fluorescent antibody (FA) test is sometimes used for the identification of _. gonorrhoeae in primary ;
isolates rom urogenital specimens. The reagent curxently -used for the F~ test is derived from the rabbit. In speci-mens from other sites, namely throat, blood, joint exudate or cerebrospinal fluid, the FA test must be supplemented by sugar fermentation procedures. Considerable experience and -costly equipment is re~uired to use the FA test for the iden~
tification of N. gonorrhoeae.
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Recently, M. B. Perry et al (Can. J. Biochem. `
53:623-629, 1975) have found that a lipopolysaccharide isolated from _. gonorrhoeae colony type 4 is common to ;
all strains of N. gonorrhoeae. This LPS is not immunogenic in rabbits, whether conjugated to a protein carrier or as such, while in mice an immunogenic effect was observed.

Summary of the Invention .
On further investigation, we have found that this common lipopolysaccharide has an active antigenic effect in fowl, e.y., hens, chickens, etc., causing the produc-tion of antibodies to N. gonorrhoeae. We have also found that these fowl antibodies are capable of agglutinating cells of all N. gonorrhoeae strains tested~ The invention is thus di-rected to this preparation of fowl antibody product and to its use in a direct agglutination test for identi~ying ..... ~ ~. -_. gonorrhoeae.

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The invention includes a method of preparing a re- "
agent comprising specific fowl antibodies causing agglutination of cells of Neisseria gonorrhoeae. This includes (a) providing lipopolysaccharide antigen which is isolated from N. gonorrhoeae colony type 4 and is common to N. gonorrhoeae, (b) inoculating live fowl with this lipopolysac-charide antigen in amounts effective to raise antibodies in the fowl, and (c) recovering blood serum containing the anti-bodies from the inoculated fowl.
As an identification test for N. gonorrhoeae, the invention includes the further steps of mixing the antibody reagent with a sample of bacterial cells to be identified, and ob-serving whether cell agglutination occurs, the occurence of agglutination being a positive test for N. gonorrhoeae.
The invention also includes the novel reagent causing agglutination o~ cells of any strain of N. gonorrhoeae comprising antibodies derived from fowl inoculated with lipo-polysaccharide antigen which is common to N. gonorrhoeae.
Both the common lipopolysaccharide antigen and the fowl host seem to be unique and critical in producing this .
type of antibody product able to agglutinate cells of all strains of M. gonorrhoeae yet not other closely related or confusingly similar species. We endeavored to use o-ther gono-coccal antigenic components to raise antisera having the same properties and were unsuccessful. Other animals were inocula-ted with the common antigen (rabbits, mlce, goats, guinea pigs and rats) but the sera recovered were unable to cause agglu-tination of all N. gonorrhoeae strains tested. Thus the com-bination of the common lipopolysaccharide antigen and the fGwl host has resulted in a uni~ue antibody product able ~`

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to serve as the key reagent in a simple agglutina-tion type identification test. ;~ -Detailed Description and Preferred Embodiments The common gonococcal antigen can be prepared as described in the above Perry et al 1975 publication. This antigen can be more fully described as follows. The lipid component (on hydrolysis, methanolysis and GLC analysis) contained about 38~ dodecanoic acid, 25% 3-hydroxydodecanoic acid and 11% 3-hydroxytetradecanoic acid. The major compo-'- ::
nent in the non-lipid portion was a core oligosaccharide of approximate molecular weight about 1570 and having the molar ratio composition as in Table 1.

Composition of N. gonorrhoeae LPS (T~
, core oligosaccharide . .
Component Molar Ratio 2-Amino-2-deoxy-D-glucose 1.97 D-Glucose 2.00 D-~alactose 2.12 L-glycero-D-manno-~eptose 0.96 3-Deoxy-D manno-octulosonic acid 0.95 -Phosphate 0.92 The overall composition of the lipopolysaccharide LPS is given in Table 2.

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TAsLE 2 ,- Composition analysis of N. yonorrhoeae (T4) LPS

Component Weight ~ .
2-Amino-2-deoxy-D-glucose 13.8 D-Glucose 6.0 D-Galactose 6.9 L-glycero-D-manno-Heptose 3.8 - 3-Deoxy-D-manno-octulosonic acid 7.3 Phosphorus 3.6 Total lipid 44.0 Ethanolamine Trace `
.
Protein 0.2 .~' .

The lipopolysaccharide antigen can be suitably in-oculated into hens as a solution in physiological saline.
A suitable inoculation dose range is from about 500;~g to about 2.S mg antigen/kg body weight. The inoculation may be repeated at weekly intervals to give increased antibody `
titers in the fowl. A preferred inoculation regime in hens and recovery of antiserum is as follows:
About 500 micrograms of gonococcal lipopolysaccharide antigen is injected once a week for three weeks. A further 2.5 milligrams i5 given two weeks after the third dose and " `
the fowl bled one week later. The blood (clotted) is held at about 40C until the serum separates. After separation, the serum is stored at a low temperature (4C or -70C).
While hens or chickens are the preferred host for inoculation, other fowl could also be used.

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The fowl antibody product can lf desired be reco-vered by fractionation procedures and stored as lyophilized powder. Before use, this recovered antibody would be dis-solved in distilled water.

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We have conducted stability studies on the antisera obtained from hens immunized with lipopolysaccharide. Serum aliquots lyophilized, or stored at -70C, -20C or at 4C, retained their activity for the full course of our study (6 months).
The antibody can be coupled to a protein or cell to give a more observable agglutination or clumping effect.
This coupling can be accomplished by reagents able to react with reactive sites of both the protein or cell and the anti- `
body, these reagents being e.g., compounds having two or more of the following reactive groups: azo, sul~onic acid, fluoro groups combined with nitro groups, azide, imine, and reactive -~
chloro groups. These reactive groups are capable of reacting with the primary amino, sulfhydryl (mercapto), and hydroxyl sites in the polymer chains of the antibody substances and .
of the protein or cell surfaces. A representative list of known coupling agents is: bis-diazobenzidine, bis-dlazoben-zidine disulfonic acid, diazotized arsanilic acid, tetraazo-p-phenylenediamine, difluorodinitrobenzene, various carbo-diimides, toluene diisocyanate, cyanuric chloride, dichloro-S-triazine, and N-t-butyl-5-methylisoxazolium perchlorate.
If desired, the antibody can also be tagged with a fluorescent or chromophoric marker as is known in the art, and the agglutination and staining effect on the cells of N. gonorrhoeae obser~ed by appropriate spectophotometric and -microscopic techniques. Fluorescein isothiocyana-te (FITC) has been found to be the most suitab]e labeling agent be-cause of its excellent fluorescent charac-teristics includinc~

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both brightness and color which make it stand out against a background. The antibody could instead be tagged with an enzyme such as peroxydase, alkaline phosphatase etc., these tagging enzymes being known in the art.
The agglutination identification test is carried out by combining the unknown culture sample with a solution of the antibody reagent preferably in the presence of buf-fered saline (preferred pH 7.2). Agglutination can be read against a dark background with the naked eye or under magni-fication. Agglutination of N. gonorrhoeae will usually occur a few seconds after admixture of antibodies and gonococci (positive test).
The test can be performed with a single colonygrown on primary isolation medium, whether or not it has been treated with oxidase reagent and is therefore non-viable.
The colony can be picked up, e.g., with a loop under a ste-reoscopic microscope and admixed directly with the specific antiserum.
It has been found that some strains of other un-~0 related types of bacteria such as some Streptococci may give positive results in the test. For instance, in extensive t~sts, 26 out of 77 strains of Streptococci were positive.
There is no problem, however, in distinguishing streptococcus from gonococcus by the oxidase test, colonial morphology and gram staining. Serogroup B Streptococci, often found in vaginal specimens, were negative in the test (except for subgroup B II).
The following Examples are illustrative. As abuEfer, Sorensen's buffered saline pH 7.2 with 0.5% formalin (0.5 ml of 37% formaldehyde in 100 ml of buffer~ was used.

Examp]e_l - Antibody Preparatio~
Five hundred microyrams of the lipopolysaccharide antigen (of the type found common to N. go _rrhoeae), in -7_ .
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physiological saline was injected intravenously via the media wing vein to white Ieghorn hens once a week for three weeks.
A further 2.5 milligrams was given two weeks after the -~
third dose and the hens were bled by heart puncture one week later. The clotted blood was held at 40C for four hours until the serum separated off. This hen serum was stored at -70 until required as a test reagent.
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Example 2 - Slide Test Two separate drops of buffer were placed on a slide sectioned off with a grease pencil, and samples of the un-known culture were emulsified into the drops to obtain a smooth suspension. Then 1 drop of the hen antiserum of Example 1 (1:4 dilution in buffer) was mixed with the cell-buffer mixture with a loop; one drop of buffer was added to the control mixture and also mixed with a loop. The slide - ~;;
was rocked gently for a few seconds and agglutination was read with the naked eye against a dark background, or faci-litated by using a magnifying lamp. Agglutination usually ~ -. . ~ .
occurred a few seconds after admixture of serum and gonococci~
The test has been performed with a single colony whether or not it had been treated with oxidase reagent and was there- -~
fore non-viahle. The colony was picked up with a 5 mm diameter loop under a stereoscopic microscope and admixed directly into both the serum dilution and buffer drops.
(Size of the drops was 0.017 ml).
Table 3 shows that cells of _. gonorrhoeae repre-senting all of the four colony types were agglutlnated by the antiserum. All of the secondary cultures (not colony ~
typed) were identified as N. gonorrhoeae by the slide ag- ;
glutination test. None of the heterologous Neisseria species -~
was agglutinated by the lipopolysaccharide antiserum.

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Agglutination of Neisseria gonorrhoeae and reaction .. .
of other Neisseria species with hen .. :.... .
lipopolysaccharide antiserum ~.
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Neisseria species NA/NT
-Neisseria gonorrhoeae Colony Type 1 7/7

4 7/7 Secondary cultures 1006/1006 Neisseria meningitidisb 0/149 `:
Neisseria lactamica 0/7 Non-pathogenic NeisseriaC 0/14 .. ~ .
aNumber of strains agglutinated/number tested bStrains tested represent all known serotypes of N. menlngitidis CRepresents all other known species of Neisseria Occasionally, when controls were rough or clumpy, the test was performed using as diluent a 1:1 mixtur.e of buffer and - :
glycerol, although with experience, clumps of rough bacteria were readily distinguishable from agglutinated cells. Ir-respective of the medium on which the culture was received whether containing antibiotics, or blood components, sero-logical identification of N. gonorrhoeae did not present .~
any problem (contrary to the difficulties encountered in a ~ -co-agglutination test where about 50~ of the gonococcal strains had to be transferred to media without blood components .
M2nck, El. 1976~ Acta path. mi.crobiol. scand. B 8~:139-14~).

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Bacterial species other than Neisseria were tested for their reactivity with hen gonococcal LPS antisera.
Forty-six strains of P. aeruginosa, 7 strains of sranhamella catarrhalis, 13 Acine-tobacter tincluding 5 strains of Morexella) and 6 Lactobacilli were not agglutinated by the antiserum.
Some strains of Streptococci were agglutinated. However, this cross-reactivity with Streptococci does not pose a se-rious problem since there is no difficulty in distinguishing colonies of Streptococci from N. gonorrhoeae either visually or with the aid of the oxidase test or gram stain.
-~ . . , In the course of extensive tests, 241 N. gonorrhoeae strains received from a local venereal disease clinic and other local agencies were used for parallel stùdies involving direct slide agglutination of the primary isolates and of the secondary cultures. In addition 24 N. meningitidis specimens were also tested in parallel. Of the gonococcal specimens, 239 (99.2~) were identified in primary cultures (Table 4) showing an excellent correlation with the serolo-gical diagnosis of secondary cultures. This procedure ena-bled an identification of N. gonorrhoeae to be made directly - ;
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from the primary isolation medium, without the 2-3 day delay generally required for the confirmation of N. gonorrhoeae by bacteriological methods. Specimens of N meningitidis were not agglutinated by the antiserum.
During these -tests, -three persons each independen-tly tested 350 strains of N. gonorrhoeae or N. meningitidis and the results were in complete agreement. This test method is rapid, does not depend upon purity plate isolation, and has the added advantage of savings in bo-th the technician's time and cost of materials which are incurred during presently used laboratory methods to identify N. gonorrhoeae. To date, a total of 1455 cultures of N. gonorrhoeae have been tested -10- , "

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w.ith the new reagent and all were agglutinated, while no other Neisseria strains reacted.

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Claims (11)

CLAIMS:

1. A method of preparing a reagent comprising antibodies causing agglutination of cells of Neisseria gonorrhoeae comprising (a) providing lipopolysaccharide antigen of the type which is common to N. gonorrhoeae, said antigen having the following components:

(b) inoculating live fowl with this lipopolysaccharide antigen in amounts effective to raise antibodies in the fowl, and (c) recovering blood serum containing the antibodies from the inoculated fowl.

2. The method of claim 1 wherein the fowl are domestic hens or chickens.

3. The method of claim 1 wherein the antibodies are recovered and purified from the serum.

CLAIMS (cont.)

4. The method of claims 1, 2 or 3 wherein the antigen core oligosaccharide has essentially the composition in molar ratio:

5. A reagent causing specific agglutination of cells of Neisseria gonorrhoeae comprising antibodies derived from fowl inoculated with lipopoly-saccharide antigen of the type which is common to N.
gonorrhoeae, said antigen being as defined in claim 1.

6. The reagent of claim 5 in lyophilized form.

7. The reagent of claim 5 in antiserum form.

8. The reagent of claims 5, 6 or 7 in a fluorescent tagged form.

9. The reagent of claims 5, 6 or 7 diluted with buffered saline.

10. The reagent of claims 5, 6 or 7 in an enzyme tagged form.

11. A method of testing the presence of bacterial cells of Neisseria gonorrhoeae comprising mixing the anti-body reagent of claim 5 with a sample of bacterial cells suspected of being N. gonorrhoeae and observing whether cell agglutination occurs, the occurrence of agglutination being a positive test for N. gonorrhoeae with the exception of interfering streptococci strains.