NDLI: Characterization of the pseudorabies virus-specific immunoglobulin M response and evaluation of its diagnostic use in pigs with preexisting immunity to the virus.

Please wait, while we are loading the content...

Year: 2016, Volume: 54

Year: 2015, Volume: 53

Year: 2014, Volume: 52

Year: 2013, Volume: 51

Year: 2012, Volume: 50

Year: 2011, Volume: 49

Year: 2010, Volume: 48

Year: 2009, Volume: 47

Year: 2008, Volume: 46

Year: 2007, Volume: 45

Year: 2006, Volume: 44

Year: 2005, Volume: 43

Year: 2004, Volume: 42

Year: 2003, Volume: 41

Year: 2002, Volume: 40

Year: 2001, Volume: 39

Year: 2000, Volume: 38

Year: 1999, Volume: 37

Year: 1998, Volume: 36

Year: 1997, Volume: 35

Year: 1996, Volume: 34

Year: 1995, Volume: 33

Year: 1994, Volume: 32

Year: 1993, Volume: 31

Year: 1993, Volume: 31, Issue: 12

Year: 1993, Volume: 31, Issue: 11

Year: 1993, Volume: 31, Issue: 10

Year: 1993, Volume: 31, Issue: 9

Construction of a bioluminescent mycobacterium and its use for assay of antimycobacterial agents.

Gene probes for identification of the botulinal neurotoxin gene and specific identification of neurotoxin types B, E, and F.

DNA-based diagnostic tests for Salmonella species targeting agfA, the structural gene for thin, aggregative fimbriae.

Hybridization probes for conventional DNA fingerprinting used as single primers in the polymerase chain reaction to distinguish strains of Cryptococcus neoformans.

Phenotypical and genotypical characterization of epidemic clumping factor-negative, oxacillin-resistant Staphylococcus aureus.

Comparison of rapid diagnostic techniques for respiratory syncytial and influenza A virus respiratory infections in young children.

Characterization of the neutralizing epitopes of VP7 of the Gottfried strain of porcine rotavirus.

Combining pooling and alternative algorithms in seroprevalence studies.

Restriction endonuclease analysis and ribotyping differentiate Pasteurella haemolytica serotype A1 isolates from cattle within a feedlot.

Characterization of the pseudorabies virus-specific immunoglobulin M response and evaluation of its diagnostic use in pigs with preexisting immunity to the virus.

Rapid competitive enzyme-linked immunosorbent assay using a monoclonal antibody reacting with a 15-kilodalton tegumental antigen of Schistosoma mansoni for serodiagnosis of schistosomiasis.

Diagnosis of Toxoplasma parasitemia in patients with AIDS by gene detection after amplification with polymerase chain reaction.

Rapid broth macrodilution method for determination of MICs for Mycobacterium avium isolates.

Evaluation of counterimmunoelectrophoresis for serotyping Actinobacillus pleuropneumoniae isolates and detection of type-specific antigens in lungs of infected pigs.

Immune response to synthetic peptides of hepatitis delta antigen.

Expression of feline immunodeficiency virus gag and env precursor proteins in Spodoptera frugiperda cells and their use in immunodiagnosis.

Preventing false positives: quantitative evaluation of three protocols for inactivation of polymerase chain reaction amplification products.

Dependence of polymerase chain reaction product inactivation protocols on amplicon length and sequence composition.

Influence of zinc on Pseudomonas aeruginosa susceptibilities to imipenem.

Evaluation of sputum smears concentrated by cytocentrifugation for detection of acid-fast bacilli.

Tentative criteria for confirming the in vitro susceptibilities of Haemophilus influenzae and Neisseria gonorrhoeae to two fluoroquinolones (sparfloxacin and levofloxacin), including quality control parameters.

Bacteremia due to Rochalimaea henselae in a child: practical identification of isolates in the clinical laboratory.

Development of a DNA probe for Streptococcus bovis by using a cloned amylase gene.

Paecilomyces variotii in peritoneal dialysate.

Automated interpretation of disk diffusion antibiotic susceptibility tests with the radial profile analysis algorithm.

Sensitive enzyme-linked immunosorbent assay for detection of Clostridium botulinum neurotoxins A, B, and E using signal amplification via enzyme-linked coagulation assay.

Detection and identification of Mycobacterium tuberculosis directly from sputum sediments by amplification of rRNA.

Epidemiological study of an Acinetobacter baumannii outbreak by using polymerase chain reaction fingerprinting.

Detection of Trypanosoma cruzi in blood specimens of chronic chagasic patients by polymerase chain reaction amplification of kinetoplast minicircle DNA: comparison with serology and xenodiagnosis.

Intrathecal immune response and virus-specific immunoglobulin M antibodies in laboratory diagnosis of acute poliomyelitis.

Analysis of acquired human cytomegalovirus infections by polymerase chain reaction.

Reactogenicity and immunogenicity of a high-titer rhesus rotavirus-based quadrivalent rotavirus vaccine.

Large-scale DNA fingerprinting of Mycobacterium tuberculosis strains as a tool for epidemiological studies of tuberculosis.

Serologic analysis of dogs, horses, and cottontail rabbits for antibodies to an antigenic flagellar epitope of Borrelia burgdorferi.

Neisseria weaveri sp. nov., formerly CDC group M-5, a gram-negative bacterium associated with dog bite wounds.

Species identification of oral viridans streptococci by restriction fragment polymorphism analysis of rRNA genes.

Epidemiologic application of a standardized ribotype scheme for Vibrio cholerae O1.

Prevalence and some properties of verotoxin (Shiga-like toxin)-producing Escherichia coli in seven different species of healthy domestic animals.

New cause for false-positive results with the Pastorex Aspergillus antigen latex agglutination test.

Detection of rotavirus serotypes G1, G2, G3, and G11 in feces of diarrheic calves by using polymerase chain reaction-derived cDNA probes.

Wound isolate of Salmonella typhimurium that became chlorate resistant after exposure to Dakin's solution: concomitant loss of hydrogen sulfide production, gas production, and nitrate reduction.

Identification of vancomycin-resistant lactic bacteria isolated from humans.

Typing of Aspergillus species and Aspergillus fumigatus isolates by interrepeat polymerase chain reaction.

Genomic fingerprinting of Neisseria meningitidis associated with group C meningococcal disease in Canada.

Rapid detection and identification of Mycobacterium avium by amplification of 16S rRNA sequences.

Clonal relationships among classical Vibrio cholerae O1 strains isolated between 1961 and 1992 in Bangladesh.

Cytopathic effect mimicking virus culture due to Mycobacterium tuberculosis.

False-negative cerebrospinal fluid cryptococcal latex agglutination tests for patients with culture-positive cryptococcal meningitis.

Mucor ramosissimus Samutsevitsch isolated from a thigh lesion.

Use of an enzyme-linked immunoassay for Clostridium difficile serogrouping.

Severe human infections caused by Vibrio metschnikovii.

Ceftizoxime interpretive criteria for in vitro susceptibility tests with Neisseria gonorrhoeae.

Reliability of cord formation in BACTEC media for presumptive identification of mycobacteria.

Incidence of Neisseria gonorrhoeae isolates negative by Syva direct fluorescent-antibody test but positive by Gen-Probe accuprobe test in a sexually transmitted disease clinic population.

Quality control guidelines for cefdinir, cefepime, cefetamet, cefmetazole, cefpodoxime, cefprozil, and clinafloxacin (CI-960) for various National Committee for Clinical Laboratory Standards susceptibility testing methods. Quality Control Study Group.

Recovery of a strain of Agrobacterium radiobacter with a mucoid phenotype from an immunocompromised child with bacteremia.

Classification of respiratory tract picornavirus isolates as enteroviruses or rhinoviruses by using reverse transcription-polymerase chain reaction.

Human papillomavirus and cutaneous warts in meat handlers.

Circulating Candida antigens and antibodies: useful markers of candidemia.

Use of selective buffered charcoal-yeast extract medium for isolation of nocardiae from mixed cultures.

Rejection criteria for endotracheal aspirates.

Diagnosis of Helicobacter pylori Infection by Using Pyloriset EIA-G and EIA-A for Detection of Serum Immunoglobulin G (IgG) and IgA Antibodies

Year: 1993, Volume: 31, Issue: 8

Year: 1993, Volume: 31, Issue: 7

Year: 1993, Volume: 31, Issue: 6

Year: 1993, Volume: 31, Issue: 5

Year: 1993, Volume: 31, Issue: 4

Year: 1993, Volume: 31, Issue: 3

Year: 1993, Volume: 31, Issue: 2

Year: 1993, Volume: 31, Issue: 1

Year: 1992, Volume: 30

Year: 1991, Volume: 29

Year: 1990, Volume: 28

Year: 1989, Volume: 27

Year: 1988, Volume: 26

Year: 1987, Volume: 25

Year: 1986, Volume: 24

Year: 1986, Volume: 23

Year: 1985, Volume: 22

Year: 1985, Volume: 21

Year: 1984, Volume: 20

Year: 1984, Volume: 19

Year: 1983, Volume: 18

Year: 1983, Volume: 17

Year: 1982, Volume: 16

Year: 1982, Volume: 15

Year: 1981, Volume: 14

Year: 1981, Volume: 13

Year: 1980, Volume: 12

Year: 1980, Volume: 11

Year: 1979, Volume: 10

Year: 1979, Volume: 9

Year: 1978, Volume: 8

Year: 1978, Volume: 7

Year: 1977, Volume: 6

Year: 1977, Volume: 5

Year: 1976, Volume: 4

Year: 1976, Volume: 3

Year: 1975, Volume: 2

Year: 1975, Volume: 1

Characterization of the pseudorabies virus-specific immunoglobulin M response and evaluation of its diagnostic use in pigs with preexisting immunity to the virus.

Content Provider	PubMed Central
Author	Kimman, T. G.
Abstract	Despite preexisting immunity to pseudorabies virus (PRV), pigs may become infected and may or may not show clinical signs of disease. To investigate whether detection of immunoglobulin M (IgM) antibodies to PRV is suitable for diagnosis of recent infection in pigs with (or without) preexisting immunity, the IgM responses of pigs were examined after both experimental and natural infections. Upon inoculation of seronegative pigs with a low dose of a mildly virulent strain of PRV, IgM was first detectable at day 7 postinoculation (p.i.), reached a maximum at day 14 p.i., and became undetectable again at about days 32 to 36 p.i. In inoculated pigs with maternal antibodies against PRV, the IgM response began later and ended sooner, and peak titers were also lower. In immune pigs with maternally derived antibodies, there was apparently no correlation between the virulence of the inoculated strain and the IgM response. The suitability of the IgM enzyme-linked immunosorbent assay (ELISA) for detection of recent infection in the field was compared with that of the virus neutralization (VN) assay and with an ELISA which specifically detects antibodies directed to glycoprotein I (gI) of PRV. Paired sera were obtained from pigs suspected of PRV infection in an area endemic for PRV infection in which vaccination against PRV is often applied. Practically all pigs had antibodies to PRV in the acute phase of the disease. Compared with the VN assay, the specificity of the IgM ELISA was high but its sensitivity was low. However, all three serotests apparently failed to detect some PRV infections. The IgM ELISA appeared to be especially useful as a diagnostic aid for detection of recent infections in pigs with high levels of neutralizing and gI antibodies, probably maternally derived, in the acute phase of the disease. Such pigs may fail to develop a significant rise in VN antibody titer. The IgM ELISA may be the only serotest for monitoring infections in such pigs.
Starting Page	2309
File Format	PDF
ISSN	1098660X
e-ISSN	1098660X
Journal	Journal of Clinical Microbiology
Issue Number	9
Volume Number	31
Language	English
Publisher Date	1993-09-01
Access Restriction	Open
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Microbiology (medical)

Central Library (ISO-9001:2015 Certified)
Indian Institute of Technology Kharagpur
Kharagpur, West Bengal, India | PIN - 721302

See location in the Map
03222 282435
Mail: support@ndl.gov.in

Sl.	Authority	Responsibilities	Communication Details
1	Ministry of Education (GoI), Department of Higher Education	Sanctioning Authority	https://www.education.gov.in/ict-initiatives
2	Indian Institute of Technology Kharagpur	Host Institute of the Project: The host institute of the project is responsible for providing infrastructure support and hosting the project	https://www.iitkgp.ac.in
3	National Digital Library of India Office, Indian Institute of Technology Kharagpur	The administrative and infrastructural headquarters of the project	Dr. B. Sutradhar bsutra@ndl.gov.in
4	Project PI / Joint PI	Principal Investigator and Joint Principal Investigators of the project	Dr. B. Sutradhar bsutra@ndl.gov.in Prof. Saswat Chakrabarti will be added soon
5	Website/Portal (Helpdesk)	Queries regarding NDLI and its services	support@ndl.gov.in
6	Contents and Copyright Issues	Queries related to content curation and copyright issues	content@ndl.gov.in
7	National Digital Library of India Club (NDLI Club)	Queries related to NDLI Club formation, support, user awareness program, seminar/symposium, collaboration, social media, promotion, and outreach	clubsupport@ndl.gov.in
8	Digital Preservation Centre (DPC)	Assistance with digitizing and archiving copyright-free printed books	dpc@ndl.gov.in
9	IDR Setup or Support	Queries related to establishment and support of Institutional Digital Repository (IDR) and IDR workshops	idr@ndl.gov.in