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Volume 6, Issue 1 (Suppl)

Clin Microbiol

ISSN: 2327-5073 CMO, an open access journal

Microbiology & Mycotoxins 2017

February 27-28, 2017

February 27-28, 2017 Amsterdam, Netherlands

7

th

Euro Global Summit on

Clinical Microbiology and Mycotoxins

Clinical findings after indoor micro-fungal and trichothecene exposure

Irene H Grant, Jack D Thrasher

and

Jake Geller

New York Medical College, USA

T

richothecenes (Ts) remain toxic despite disinfection, bind dust, damage skin/mucosa/phagocytes/neurons. Monitoring 45

patients (adults, children, embryos) exposed to 18 Ts-contaminated indoor-environments, fungal IgGs, urine mycotoxins (MCTs)

[Ts, ochratoxin (OTA), aflatoxin (A)], immune parameters (neutrophils, lymphocyte subsets, monocytes, IgG, IgA, IgM, IgE and

subclasses), immunosuppressant medications, nutritional deficiencies (protein, Vitamin D, zinc), genetic MTHFR single-nucleotide-

polymorphisms C677T&A1298C, environmental contamination severity (ECS), hazardous activity severity (HAS), exposure duration

(ED) and clinical findings were rated sorting by disease severity (DS). Bio-statistical analysis correlated DS, ECS, HAS and ED by

using Pearson correlation coefficients.

Aspergillus/Penicillium

(A/P) detected in all 18 Ts-contaminated environments (56% A.

niger

),

Chaetomium

94%,

Stachybotrys

(St) 67%,

Mucor

61%,

Alternaria

44% and 33%

P. brevicompactum

. None had

Fusarium

. Patient

outcomes were: Disabled 54% (23% permanently), neurologic 67% (female predominance), ear/nose/throat 30%, pulmonary 21%

(male predominance) and dermatologic 12%. IgG titers: A/P+93% (91% of the moderately-to-extremely ill, females predominant).

None of the mildly-ill had elevated

A. fumigatus

IgG, P-IgG titers+86%

(P. notatum/P. chrysogenum

74% tested); St 59% (St-IgG+61%

and St-IgA+22% of the moderate-extremely-ill and none of the mildly-ill).

Phoma, Trichoderma

IGGs were elevated and more in

males;

A. fumigatus

IgG, A antigen EIA and

P. notatum

IGG were more in females. Urinary MCTs (91% tested): detectable Ts 97%

(trace 38%, elevated 46%); 31% OTA, 6% A. All extremely-ill excreted Ts; none excreted A. Higher Ts predominated in females (46%

vs. 24%), trace inmales (38% vs. 18%). Overall, disease severity strongly correlated with ECS (p=0.00000001) and HAS (p=0.0000001).

Surprisingly, ED had insignificant correlation. The strongest DS vs. ECS predictors were mucosal injury (p=0.00000003), any detection

of urinary Ts (p=0.0000001) and the development of fungal IGGs (p=.0000009). DS also strongly correlated with HAS, particularly

with genetic MTHFR detoxification defects (p=0.00000008).

Biography

Irene H Grant is an Infectious Disease Specialist trained by Donald Armstrong at Memorial Sloan Kettering. She is a Clinical Assistant Professor of Medicine at NY

Medical College. She has a large practice of treating mold-exposure illness. She is an Albert Einstein College of Medicine graduate. She is knowledgeable and

experienced in the complexities and limitations in microbiologic diagnostic Mycological testing, Microbiology-Mycology reporting, as well as the failure on the part

of physicians to request the Microbiology and/or Pathology Laboratories to perform non-routine specialty studies.

ihg1md@gmail.com

Irene H Grant et al., Clin Microbiol 2017, 6:1(Suppl)

http://dx.doi.org/10.4172/2327-5073.C1.027